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Publications by Faysal Gok

Newly Discovered Mutations in the GALNT3 Gene Causing Autosomal Recessive Hyperostosis-Hyperphosphatemia Syndrome

Acta Orthopaedica
MedicineSurgeryOrthopedicsSports Medicine
2009English

Related publications

Mutations in the Nebulin Gene Associated With Autosomal Recessive Nemaline Myopathy

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
1999English

Mutations in GRHL2 Result in an Autosomal-Recessive Ectodermal Dysplasia Syndrome

American Journal of Human Genetics
Genetics
2014English

Loss-Of-Function Mutations in HPSE2 Cause the Autosomal Recessive Urofacial Syndrome

American Journal of Human Genetics
Genetics
2010English

Mutations in EOGT Confirm the Genetic Heterogeneity of Autosomal-Recessive Adams-Oliver Syndrome

American Journal of Human Genetics
Genetics
2013English

Autosomal Recessive Chorioretinopathy-Microcephaly Syndrome

2020English

New Autosomal Recessive Faciodigitogenital Syndrome.

Journal of Medical Genetics
Genetics
1988English

Autosomal Recessive Distal Osteolysis Syndrome

2020English

Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability

American Journal of Human Genetics
Genetics
2012English

Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts

American Journal of Human Genetics
Genetics
2011English

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