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Publications by Fatema Al-Zahrani
Mutations in EOGT Confirm the Genetic Heterogeneity of Autosomal-Recessive Adams-Oliver Syndrome
American Journal of Human Genetics
Genetics
Related publications
Loss-Of-Function Mutations in HPSE2 Cause the Autosomal Recessive Urofacial Syndrome
American Journal of Human Genetics
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Mutations in GRHL2 Result in an Autosomal-Recessive Ectodermal Dysplasia Syndrome
American Journal of Human Genetics
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Novel Mutations Confirm That COL11A2 Is Responsible for Autosomal Recessive Non-Syndromic Hearing Loss DFNB53
Molecular Genetics and Genomics
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Newly Discovered Mutations in the GALNT3 Gene Causing Autosomal Recessive Hyperostosis-Hyperphosphatemia Syndrome
Acta Orthopaedica
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Orthopedics
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Current Opinion in the Molecular Genetics of Adams-Oliver Syndrome
Expert Opinion on Orphan Drugs
Toxicology
Pharmaceutics
Pharmacology
Health Policy
Autosomal Recessive Chorioretinopathy-Microcephaly Syndrome
New Autosomal Recessive Faciodigitogenital Syndrome.
Journal of Medical Genetics
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Autosomal Recessive Distal Osteolysis Syndrome
Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability
American Journal of Human Genetics
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