FGFR1 c.*1632A>G

Variant ID: 8-38269514-T-C

NM_023110.2(FGFR1):c.*1632A>G

This variant was identified in 39 publications

View GRCh38 version.




Publications:


Evidence for a genetic contribution to the ossification of spinal ligaments in Ossification of Posterior Longitudinal Ligament and Diffuse idiopathic skeletal hyperostosis: A narrative review.

Frontiers In Genetics
Couto, Ana Rita AR; Parreira, Bruna B; Power, Deborah M DM; Pinheiro, Luís L; Madruga Dias, João J; Novofastovski, Irina I; Eshed, Iris I; Sarzi-Puttini, Piercarlo P; Pappone, Nicola N; Atzeni, Fabiola F; Verlaan, Jorrit-Jan JJ; Kuperus, Jonneke J; Bieber, Amir A; Ambrosino, Pasquale P; Kiefer, David D; Khan, Muhammad Asim MA; Mader, Reuven R; Baraliakos, Xenofon X; Bruges-Armas, Jácome J
Publication Date: 2022

Variant appearance in text: rs13317
PubMed Link: 36276944
Variant Present in the following documents:
  • Main text
  • fgene-13-987867.pdf
View BVdb publication page



Case Report: Primary Leptomeningeal Medulloblastoma in a Child: Clinical Case Report and Literature Review.

Frontiers In Pediatrics
Morgacheva, Daria D; Daks, Alexandra A; Smirnova, Anna A; Kim, Aleksandr A; Ryzhkova, Daria D; Mitrofanova, Lubov L; Staliarova, Alena A; Omelina, Evgeniya E; Pindyurin, Alexey A; Fedorova, Olga O; Shuvalov, Oleg O; Petukhov, Alexey A; Dinikina, Yulia Y
Publication Date: 2022

Variant appearance in text: rs13317
PubMed Link: 35899134
Variant Present in the following documents:
  • Table_1.xlsx, sheet 1
View BVdb publication page



Tendon and Ligament Genetics: How Do They Contribute to Disease and Injury? A Narrative Review.

Life (Basel, Switzerland)
Ribbans, William J WJ; September, Alison V AV; Collins, Malcolm M
Publication Date: 2022-04-29

Variant appearance in text: rs13317
PubMed Link: 35629331
Variant Present in the following documents:
  • Main text
  • life-12-00663.pdf
View BVdb publication page



Effects of Genetic Variation on Endurance Performance, Muscle Strength, and Injury Susceptibility in Sports: A Systematic Review.

Frontiers In Physiology
Appel, Milena M; Zentgraf, Karen K; Krüger, Karsten K; Alack, Katharina K
Publication Date: 2021

Variant appearance in text: rs13317
PubMed Link: 34366884
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association between miRNA Target Sites and Incidence of Primary Osteoarthritis in Women from Volga-Ural Region of Russia: A Case-Control Study.

Diagnostics (Basel, Switzerland)
Tyurin, Anton A; Shapovalova, Daria D; Gantseva, Halida H; Pavlov, Valentin V; Khusainova, Rita R
Publication Date: 2021-07-06

Variant appearance in text: rs13317
PubMed Link: 34359306
Variant Present in the following documents:
  • Main text
  • diagnostics-11-01222.pdf
View BVdb publication page



Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy.

Bmc Cardiovascular Disorders
Lin, Xiaoping X; Ma, Yuankun Y; Cai, Zhejun Z; Wang, Qiyuan Q; Wang, Lihua L; Huo, Zhaoxia Z; Hu, Dan D; Wang, Jian'an J; Xiang, Meixiang M
Publication Date: 2020-02-11

Variant appearance in text: rs13317
PubMed Link: 32046637
Variant Present in the following documents:
  • 12872_2020_1369_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



Genetics of Degenerative Cervical Myelopathy: A Systematic Review and Meta-Analysis of Candidate Gene Studies.

Journal Of Clinical Medicine
Pope, Daniel H DH; Davies, Benjamin M BM; Mowforth, Oliver D OD; Bowden, A Ramsay AR; Kotter, Mark R N MRN
Publication Date: 2020-01-20

Variant appearance in text: rs13317
PubMed Link: 31968564
Variant Present in the following documents:
  • Main text
  • jcm-09-00282.pdf
View BVdb publication page



Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports SH3PXD2A as a Clefting Susceptibility Gene.

Genes
van Rooij, Iris Alm IA; Ludwig, Kerstin U KU; Welzenbach, Julia J; Ishorst, Nina N; Thonissen, Michelle M; Galesloot, Tessel E TE; Ongkosuwito, Edwin E; Bergé, Stefaan J SJ; Aldhorae, Khalid K; Rojas-Martinez, Augusto A; Kiemeney, Lambertus Alm LA; Vermeesch, Joris Robert JR; Brunner, Han H; Roeleveld, Nel N; Devriendt, Koen K; Dormaar, Titiaan T; Hens, Greet G; Knapp, Michael M; Carels, Carine C; Mangold, Elisabeth E
Publication Date: 2019-12-07

Variant appearance in text: rs13317
PubMed Link: 31817908
Variant Present in the following documents:
  • Main text
  • genes-10-01023.pdf
View BVdb publication page



PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology
Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S
Publication Date: 2019-10-22

Variant appearance in text: rs13317
PubMed Link: 31640808
Variant Present in the following documents:
  • 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft.

Plos Genetics
Huang, Lulin L; Jia, Zhonglin Z; Shi, Yi Y; Du, Qin Q; Shi, Jiayu J; Wang, Ziyan Z; Mou, Yandong Y; Wang, Qingwei Q; Zhang, Bihe B; Wang, Qing Q; Ma, Shi S; Lin, He H; Duan, Shijun S; Yin, Bin B; Lin, Yansong Y; Wang, Yiru Y; Jiang, Dan D; Hao, Fang F; Zhang, Lin L; Wang, Haixin H; Jiang, Suyuan S; Xu, Huijuan H; Yang, Chengwei C; Li, Chenghao C; Li, Jingtao J; Shi, Bing B; Yang, Zhenglin Z
Publication Date: 2019-10

Variant appearance in text: rs13317
PubMed Link: 31609978
Variant Present in the following documents:
  • Main text
  • pgen.1008357.pdf
View BVdb publication page



MicroRNA-374a, -4680, and -133b suppress cell proliferation through the regulation of genes associated with human cleft palate in cultured human palate cells.

Bmc Medical Genomics
Suzuki, Akiko A; Li, Aimin A; Gajera, Mona M; Abdallah, Nada N; Zhang, Musi M; Zhao, Zhongming Z; Iwata, Junichi J
Publication Date: 2019-07-01

Variant appearance in text: rs13317
PubMed Link: 31262291
Variant Present in the following documents:
  • 12920_2019_546_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page



Genetics of rotator cuff tears: no association of col5a1 gene in a case-control study.

Bmc Medical Genetics
Longo, Umile Giuseppe UG; Margiotti, Katia K; Petrillo, Stefano S; Rizzello, Giacomo G; Fusilli, Caterina C; Maffulli, Nicola N; De Luca, Alessandro A; Denaro, Vincenzo V
Publication Date: 2018-12-20

Variant appearance in text: rs13317
PubMed Link: 30572822
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genomic analyses in African populations identify novel risk loci for cleft palate.

Human Molecular Genetics
Butali, Azeez A; Mossey, Peter A PA; Adeyemo, Wasiu L WL; Eshete, Mekonen A MA; Gowans, Lord J J LJJ; Busch, Tamara D TD; Jain, Deepti D; Yu, Wenjie W; Huan, Liu L; Laurie, Cecelia A CA; Laurie, Cathy C CC; Nelson, Sarah S; Li, Mary M; Sanchez-Lara, Pedro A PA; Magee, William P WP; Magee, Kathleen S KS; Auslander, Allyn A; Brindopke, Frederick F; Kay, Denise M DM; Caggana, Michele M; Romitti, Paul A PA; Mills, James L JL; Audu, Rosemary R; Onwuamah, Chika C; Oseni, Ganiyu O GO; Owais, Arwa A; James, Olutayo O; Olaitan, Peter B PB; Aregbesola, Babatunde S BS; Braimah, Ramat O RO; Oginni, Fadekemi O FO; Oladele, Ayodeji O AO; Bello, Saidu A SA; Rhodes, Jennifer J; Shiang, Rita R; Donkor, Peter P; Obiri-Yeboah, Solomon S; Arthur, Fareed Kow Nanse FKN; Twumasi, Peter P; Agbenorku, Pius P; Plange-Rhule, Gyikua G; Oti, Alexander Acheampong AA; Ogunlewe, Olugbenga M OM; Oladega, Afisu A AA; Adekunle, Adegbayi A AA; Erinoso, Akinwunmi O AO; Adamson, Olatunbosun O OO; Elufowoju, Abosede A AA; Ayelomi, Oluwanifemi I OI; Hailu, Taiye T; Hailu, Abiye A; Demissie, Yohannes Y; Derebew, Miliard M; Eliason, Steve S; Romero-Bustillous, Miguel M; Lo, Cynthia C; Park, James J; Desai, Shaan S; Mohammed, Muiawa M; Abate, Firke F; Abdur-Rahman, Lukman O LO; Anand, Deepti D; Saadi, Irfaan I; Oladugba, Abimibola V AV; Lachke, Salil A SA; Amendt, Brad A BA; Rotimi, Charles N CN; Marazita, Mary L ML; Cornell, Robert A RA; Murray, Jeffrey C JC; Adeyemo, Adebowale A AA
Publication Date: 2019-03-15

Variant appearance in text: rs13317
PubMed Link: 30452639
Variant Present in the following documents:
  • Main text
View BVdb publication page



Six NSCL/P Loci Show Associations With Normal-Range Craniofacial Variation.

Frontiers In Genetics
Indencleef, Karlijne K; Roosenboom, Jasmien J; Hoskens, Hanne H; White, Julie D JD; Shriver, Mark D MD; Richmond, Stephen S; Peeters, Hilde H; Feingold, Eleanor E; Marazita, Mary L ML; Shaffer, John R JR; Weinberg, Seth M SM; Hens, Greet G; Claes, Peter P
Publication Date: 2018

Variant appearance in text: rs13317
PubMed Link: 30410503
Variant Present in the following documents:
  • Main text
  • fgene-09-00502.pdf
View BVdb publication page



Molecular pathogenesis of fracture nonunion.

Journal Of Orthopaedic Translation
Ding, Zi-Chuan ZC; Lin, Yi-Kai YK; Gan, Yao-Kai YK; Tang, Ting-Ting TT
Publication Date: 2018-07

Variant appearance in text: rs13317
PubMed Link: 30035032
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Genetic Variants Associated with Clinicopathological Profiles in Sporadic Breast Cancer in Sri Lankan Women.

Journal Of Breast Cancer
Sirisena, Nirmala Dushyanthi ND; Adeyemo, Adebowale A; Kuruppu, Anchala Ishani AI; Samaranayake, Nilakshi N; Dissanayake, Vajira Harshadeva Weerabaddana VHW
Publication Date: 2018-06

Variant appearance in text: rs13317
PubMed Link: 29963112
Variant Present in the following documents:
  • Main text
  • jbc-21-165.pdf
View BVdb publication page



Genome-wide association study identifies a locus associated with rotator cuff injury.

Plos One
Roos, Thomas R TR; Roos, Andrew K AK; Avins, Andrew L AL; Ahmed, Marwa A MA; Kleimeyer, John P JP; Fredericson, Michael M; Ioannidis, John P A JPA; Dragoo, Jason L JL; Kim, Stuart K SK
Publication Date: 2017

Variant appearance in text: rs13317
PubMed Link: 29228018
Variant Present in the following documents:
  • Main text
  • pone.0189317.pdf
View BVdb publication page



Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10

Variant appearance in text: rs13317
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 1
  • oncotarget-08-95841-s002.xlsx, sheet 4
View BVdb publication page



The Pathogenesis of Ossification of the Posterior Longitudinal Ligament.

Aging And Disease
Yan, Liang L; Gao, Rui R; Liu, Yang Y; He, Baorong B; Lv, Shemin S; Hao, Dingjun D
Publication Date: 2017-10

Variant appearance in text: rs13317
PubMed Link: 28966802
Variant Present in the following documents:
  • Main text
  • ad-8-5-570.pdf
View BVdb publication page



Genetic Factors in Tendon Injury: A Systematic Review of the Literature.

Orthopaedic Journal Of Sports Medicine
Vaughn, Natalie H NH; Stepanyan, Hayk H; Gallo, Robert A RA; Dhawan, Aman A
Publication Date: 2017-08

Variant appearance in text: rs13317
PubMed Link: 28856171
Variant Present in the following documents:
  • Main text
View BVdb publication page



Targeted sequencing in FGF/FGFR genes and association analysis of variants for mandibular prognathism.

Medicine
Xiong, Xueyan X; Li, Shuyuan S; Cai, Ying Y; Chen, Fengshan F
Publication Date: 2017-06

Variant appearance in text: rs13317
PubMed Link: 28640125
Variant Present in the following documents:
  • Main text
  • medi-96-e7240.pdf
View BVdb publication page



Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity.

Nature Communications
Yu, Yanqin Y; Zuo, Xianbo X; He, Miao M; Gao, Jinping J; Fu, Yuchuan Y; Qin, Chuanqi C; Meng, Liuyan L; Wang, Wenjun W; Song, Yaling Y; Cheng, Yong Y; Zhou, Fusheng F; Chen, Gang G; Zheng, Xiaodong X; Wang, Xinhuan X; Liang, Bo B; Zhu, Zhengwei Z; Fu, Xiazhou X; Sheng, Yujun Y; Hao, Jiebing J; Liu, Zhongyin Z; Yan, Hansong H; Mangold, Elisabeth E; Ruczinski, Ingo I; Liu, Jianjun J; Marazita, Mary L ML; Ludwig, Kerstin U KU; Beaty, Terri H TH; Zhang, Xuejun X; Sun, Liangdan L; Bian, Zhuan Z
Publication Date: 2017-02-24

Variant appearance in text: rs13317
PubMed Link: 28232668
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic and familial predisposition to rotator cuff disease: a systematic review.

Journal Of Shoulder And Elbow Surgery
Dabija, Dominique I DI; Gao, Chan C; Edwards, Todd L TL; Kuhn, John E JE; Jain, Nitin B NB
Publication Date: 2017-06

Variant appearance in text: rs13317
PubMed Link: 28162885
Variant Present in the following documents:
  • Main text
View BVdb publication page



Contribution of FGFR1 Variants to Craniofacial Variations in East Asians.

Plos One
Adel, Mohamed M; Yamaguchi, Tetsutaro T; Tomita, Daisuke D; Nakawaki, Takatoshi T; Kim, Yong-Il YI; Hikita, Yu Y; Haga, Shugo S; Takahashi, Masahiro M; Nadim, Mohamed A MA; Kawaguchi, Akira A; Isa, Mutsumi M; El-Kenany, Walid H WH; El-Kadi, Abbadi A AA; Park, Soo-Byung SB; Ishida, Hajime H; Maki, Koutaro K; Kimura, Ryosuke R
Publication Date: 2017

Variant appearance in text: rs13317
PubMed Link: 28129408
Variant Present in the following documents:
  • Main text
  • pone.0170645.pdf
View BVdb publication page



Associations between microRNA binding site SNPs in FGFs and FGFRs and the risk of non-syndromic orofacial cleft.

Scientific Reports
Li, Dandan D; Zhang, Hongchuang H; Ma, Lan L; Han, Yue Y; Xu, Min M; Wang, Zhendong Z; Jiang, Hongbing H; Zhang, Weibing W; Wang, Lin L; Pan, Yongchu Y
Publication Date: 2016-08-11

Variant appearance in text: rs13317
PubMed Link: 27511275
Variant Present in the following documents:
  • Main text
  • srep31054.pdf
View BVdb publication page



Pharmacogenetic analysis of cinacalcet response in secondary hyperparathyroidism patients.

Drug Design, Development And Therapy
Jeong, Sohyun S; Kim, In-Wha IW; Oh, Kook-Hwan KH; Han, Nayoung N; Joo, Kwon Wook KW; Kim, Hyo Jin HJ; Oh, Jung Mi JM
Publication Date: 2016

Variant appearance in text: rs13317
PubMed Link: 27468225
Variant Present in the following documents:
  • Main text
View BVdb publication page



Targeted next-generation sequencing reveals multiple deleterious variants in OPLL-associated genes.

Scientific Reports
Chen, Xin X; Guo, Jun J; Cai, Tao T; Zhang, Fengshan F; Pan, Shengfa S; Zhang, Li L; Wang, Shaobo S; Zhou, Feifei F; Diao, Yinze Y; Zhao, Yanbin Y; Chen, Zhen Z; Liu, Xiaoguang X; Chen, Zhongqiang Z; Liu, Zhongjun Z; Sun, Yu Y; Du, Jie J
Publication Date: 2016-06-01

Variant appearance in text: rs13317
PubMed Link: 27246988
Variant Present in the following documents:
  • Main text
  • srep26962-s1.pdf
  • srep26962.pdf
View BVdb publication page



Genome-wide association study combined with biological context can reveal more disease-related SNPs altering microRNA target seed sites.

Bmc Genomics
Wu, Di D; Yang, Gang G; Zhang, Lifang L; Xue, Jiwei J; Wen, Zhining Z; Li, Menglong M
Publication Date: 2014-08-08

Variant appearance in text: rs13317
PubMed Link: 25106527
Variant Present in the following documents:
  • Main text
  • 12864_2014_Article_6678.pdf
View BVdb publication page



Involvement of fibroblast growth factor receptor genes in benign prostate hyperplasia in a Korean population.

Disease Markers
Park, Hae Jeong HJ; Kim, Su Kang SK; Kim, Jong Woo JW; Lee, Sang Hyub SH; Yoo, Koo Han KH; Chung, Joo-Ho JH
Publication Date: 2013

Variant appearance in text: rs13317
PubMed Link: 24385678
Variant Present in the following documents:
  • Main text
  • DM35-06-792941.pdf
View BVdb publication page



Genetic predictors of response to serotonergic and noradrenergic antidepressants in major depressive disorder: a genome-wide analysis of individual-level data and a meta-analysis.

Plos Medicine
Tansey, Katherine E KE; Guipponi, Michel M; Perroud, Nader N; Bondolfi, Guido G; Domenici, Enrico E; Evans, David D; Hall, Stephanie K SK; Hauser, Joanna J; Henigsberg, Neven N; Hu, Xiaolan X; Jerman, Borut B; Maier, Wolfgang W; Mors, Ole O; O'Donovan, Michael M; Peters, Tim J TJ; Placentino, Anna A; Rietschel, Marcella M; Souery, Daniel D; Aitchison, Katherine J KJ; Craig, Ian I; Farmer, Anne A; Wendland, Jens R JR; Malafosse, Alain A; Holmans, Peter P; Lewis, Glyn G; Lewis, Cathryn M CM; Stensbøl, Tine Bryan TB; Kapur, Shitij S; McGuffin, Peter P; Uher, Rudolf R
Publication Date: 2012

Variant appearance in text: rs13317
PubMed Link: 23091423
Variant Present in the following documents:
  • pmed.1001326.s001.pdf
View BVdb publication page



Association study of fibroblast growth factor 2 and fibroblast growth factor receptors gene polymorphism in korean ossification of the posterior longitudinal ligament patients.

Journal Of Korean Neurosurgical Society
Jun, Jae-Kyun JK; Kim, Sung-Min SM
Publication Date: 2012-07

Variant appearance in text: rs13317
PubMed Link: 22993671
Variant Present in the following documents:
  • Main text
View BVdb publication page



The influence of genetics on response to treatment with ranibizumab (Lucentis) for age-related macular degeneration: the Lucentis Genotype Study (an American Ophthalmological Society thesis).

Transactions Of The American Ophthalmological Society
Francis, Peter James PJ
Publication Date: 2011-12

Variant appearance in text: rs13317
PubMed Link: 22253485
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic studies in the Nigerian population implicate an MSX1 mutation in complex oral facial clefting disorders.

The Cleft Palate-Craniofacial Journal : Official Publication Of The American Cleft Palate-Craniofacial Association
Butali, A A; Mossey, P A PA; Adeyemo, W L WL; Jezewski, P A PA; Onwuamah, C K CK; Ogunlewe, M O MO; Ugboko, V I VI; Adejuyigbe, O O; Adigun, A I AI; Abdur-Rahman, L O LO; Onah, I I II; Audu, R A RA; Idigbe, E O EO; Mansilla, M A MA; Dragan, E A EA; Petrin, A L AL; Bullard, S A SA; Uduezue, A O AO; Akpata, O O; Osaguona, A O AO; Olasoji, H O HO; Ligali, T O TO; Kejeh, B M BM; Iseh, K R KR; Olaitan, P B PB; Adebola, A R AR; Efunkoya, E E; Adesina, O A OA; Oluwatosin, O M OM; Murray, J C JC; ,
Publication Date: 2011-11

Variant appearance in text: rs13317
PubMed Link: 21740177
Variant Present in the following documents:
  • Main text
View BVdb publication page



AXIS inhibition protein 2, orofacial clefts and a family history of cancer.

Journal Of The American Dental Association (1939)
Menezes, Renato R; Marazita, Mary Louise ML; Goldstein McHenry, Toby T; Cooper, Margaret E ME; Bardi, Kathleen K; Brandon, Carla C; Letra, Ariadne A; Martin, Rick A RA; Vieira, Alexandre Rezende AR
Publication Date: 2009-01

Variant appearance in text: rs13317
PubMed Link: 19119171
Variant Present in the following documents:
  • Main text
View BVdb publication page



Studies of genes in the FGF signaling pathway and oral clefts with or without dental anomalies.

American Journal Of Medical Genetics. Part A
Menezes, Renato R; Letra, Ariadne A; Ruff, Joe J; Granjeiro, Jose M JM; Vieira, Alexandre R AR
Publication Date: 2008-06-15

Variant appearance in text: rs13317
PubMed Link: 18478591
Variant Present in the following documents:
  • Main text
View BVdb publication page



A genome-wide linkage scan for cleft lip and cleft palate identifies a novel locus on 8p11-23.

American Journal Of Medical Genetics. Part A
Riley, B M BM; Schultz, R E RE; Cooper, M E ME; Goldstein-McHenry, T T; Daack-Hirsch, S S; Lee, K T KT; Dragan, E E; Vieira, A R AR; Lidral, A C AC; Marazita, M L ML; Murray, J C JC
Publication Date: 2007-04-15

Variant appearance in text: rs13317
PubMed Link: 17366557
Variant Present in the following documents:
  • Main text
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Impaired FGF signaling contributes to cleft lip and palate.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Riley, Bridget M BM; Mansilla, M Adela MA; Ma, Jinghong J; Daack-Hirsch, Sandra S; Maher, Brion S BS; Raffensperger, Lisa M LM; Russo, Erilynn T ET; Vieira, Alexandre R AR; Dodé, Catherine C; Mohammadi, Moosa M; Marazita, Mary L ML; Murray, Jeffrey C JC
Publication Date: 2007-03-13

Variant appearance in text: rs13317
PubMed Link: 17360555
Variant Present in the following documents:
  • Main text
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Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis.

American Journal Of Medical Genetics. Part A
Vieira, Alexandre R AR; Modesto, Adriana A; Meira, Raquel R; Barbosa, Anna Renata Schneider AR; Lidral, Andrew C AC; Murray, Jeffrey C JC
Publication Date: 2007-03-15

Variant appearance in text: rs13317
PubMed Link: 17318851
Variant Present in the following documents:
  • Main text
View BVdb publication page