Publications:

Fibrillin-1 gene mutations in a Chinese cohort with congenital ectopia lentis: spectrum and genotype-phenotype analysis.

The British Journal Of Ophthalmology

Chen, Zexu Z; Chen, Tianhui T; Zhang, Min M; Chen, Jiahui J; Deng, Michael M; Zheng, Jialei J; Lan, Li-Na LN; Jiang, Yongxiang Y

Publication Date: 2022-12

Variant appearance in text: FBN1: 4864T>C; Cys1622Arg

PubMed Link: 34281902

Variant Present in the following documents:

• bjophthalmol-2021-319084supp004.pdf
• bjophthalmol-2021-319084supp003.pdf

View BVdb publication page

Need for high-resolution Genetic Analysis in iPSC: Results and Lessons from the ForIPS Consortium.

Scientific Reports

Popp, Bernt B; Krumbiegel, Mandy M; Grosch, Janina J; Sommer, Annika A; Uebe, Steffen S; Kohl, Zacharias Z; Plötz, Sonja S; Farrell, Michaela M; Trautmann, Udo U; Kraus, Cornelia C; Ekici, Arif B AB; Asadollahi, Reza R; Regensburger, Martin M; Günther, Katharina K; Rauch, Anita A; Edenhofer, Frank F; Winkler, Jürgen J; Winner, Beate B; Reis, André A

Publication Date: 2018-11-21

Variant appearance in text: FBN1: 4864T>C; Cys1622Arg

PubMed Link: 30464253

Variant Present in the following documents:

• 41598_2018_35506_MOESM5_ESM.xlsx, sheet 5
• 41598_2018_35506_MOESM5_ESM.xlsx, sheet 4

View BVdb publication page

Whole exome sequencing is an efficient, sensitive and specific method of mutation detection in osteogenesis imperfecta and Marfan syndrome.

Bonekey Reports

McInerney-Leo, Aideen M AM; Marshall, Mhairi S MS; Gardiner, Brooke B; Coucke, Paul J PJ; Van Laer, Lut L; Loeys, Bart L BL; Summers, Kim M KM; Symoens, Sofie S; West, Jennifer A JA; West, Malcolm J MJ; Paul Wordsworth, B B; Zankl, Andreas A; Leo, Paul J PJ; Brown, Matthew A MA; Duncan, Emma L EL

Publication Date: 2013

Variant appearance in text: FBN1: 4864T>C; C1622R

PubMed Link: 24501682

Variant Present in the following documents:

• Main text

View BVdb publication page