Identity-by-descent–guided mutation analysis and exome sequencing in consanguineous families reveals unusual clinical and molecular findings in retinal dystrophy-Reference-Cited by-同舟云学术

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Identity-by-descent–guided mutation analysis and exome sequencing in consanguineous families reveals unusual clinical and molecular findings in retinal dystrophy

Published:2014-09 Issue:9 Volume:16 Page:671-680
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Coppieters Frauke,Van Schil Kristof,Bauwens Miriam,Verdin Hannah,De Jaegher Annelies,Syx Delfien,Sante Tom,Lefever Steve,Abdelmoula Nouha Bouayed,Depasse Fanny,Casteels Ingele,de Ravel Thomy,Meire Françoise,Leroy Bart P.,De Baere Elfride

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/gim201424.pdf

Reference38 articles.

1. RetNet, the Retinal Information Network. http://www.sph.uth.tmc.edu/RetNet. Accessed July 25th, 2013.

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