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Publications by Fowzan Alkuraya
Syndromic Congenital Sensorineural Deafness, Microtia and Microdontia Resulting From a Novel Homoallelic Mutation in Fibroblast Growth Factor 3 (FGF3)
European Journal of Human Genetics
Genetics
Related publications
Novel Fibroblast Growth Factor Receptor 1 Mutations in Patients With Congenital Hypogonadotropic Hypogonadism With and Without Anosmia
Journal of Clinical Endocrinology and Metabolism
Biochemistry
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Clinical Biochemistry
Medicine
Metabolism
Diabetes
1201 Whole Exon Deletion in the Claudin 16 Gene, a Novel Mutation in Familial Hypomagnesemia/Hypercalciuria/Nephrocalcinosis (FHHNC) and Sensorineural Deafness (SND)
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Mutation Spectrum of Common Deafness-Causing Genes in Patients With Non-Syndromic Deafness in the Xiamen Area, China
PLoS ONE
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Hearing Loss in Congenital Microtia
Fibroblast Growth Factor Receptor 3-IIIc Mediates Colorectal Cancer Growth and Migration
British Journal of Cancer
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Aging and Deafness. Long Term Observation of Sensorineural Deafness.
AUDIOLOGY JAPAN
A Novel De Novo Dominant Mutation of NOTCH1 Gene in an Iranian Family With Non‐syndromic Congenital Heart Disease
Journal of Clinical Laboratory Analysis
Allergy
Immunology
Biochemistry
Public Health
Medical Laboratory Technology
Clinical Biochemistry
Hematology
Microbiology
Environmental
Occupational Health
Visual Impairment in Severe and Profound Sensorineural Deafness.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Ectodermal Dysplasia-Sensorineural Deafness Syndrome
