Genotype–phenotype correlation inCC2D2A-related Joubert syndrome reveals an association with ventriculomegaly and seizures-Reference-Cited by-同舟云学术

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Genotype–phenotype correlation inCC2D2A-related Joubert syndrome reveals an association with ventriculomegaly and seizures

Published:2012-01-12 Issue:2 Volume:49 Page:126-137
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:J Med Genet

Author:

Bachmann-Gagescu Ruxandra,Ishak Gisele E,Dempsey Jennifer C,Adkins Jonathan,O'Day Diana,Phelps Ian G,Gunay-Aygun Meral,Kline Antonie D,Szczaluba Krzysztof,Martorell Loreto,Alswaid Abdulrahman,Alrasheed Shatha,Pai Shashidhar,Izatt Louise,Ronan Anne,Parisi Melissa A,Mefford Heather,Glass Ian,Doherty Dan

Publisher

BMJ

Subject

Genetics(clinical),Genetics

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