Zain Dardas
0000-0003-2387-3122
Baylor College of Medicine
14 papers found
Refreshing results…
NODAL variants are associated with a continuum of laterality defects from simple D-transposition of the great arteries to heterotaxy
HMZDupFinder: a robust computational approach for detecting intragenic homozygous duplications from exome sequencing data
SLC26A4 Phenotypic Variability Influences Intra- and Inter-Familial Diagnosis and Management
Long read sequencing and expression studies ofAHDC1deletions in Xia‐Gibbs syndrome reveal a novel genetic regulatory mechanism
Unique Variant Spectrum in a Jordanian Cohort with Inherited Retinal Dystrophies
<p>Effect of Genetic Testing on Diagnosing Gastrointestinal Pediatric Patients with Previously Undiagnosed Diseases</p>
Clinical heterogeneity in retinitis pigmentosa caused by variants in RP1 and RLBP1 in five extended consanguineous pedigrees.
Enteric anendocrinosis attributable to a novel Neurogenin-3 variant
The impact of exome sequencing on the diagnostic yield of muscular dystrophies in consanguineous families
Extending the spectrum of CLRN1 ‐ and ABCA4 ‐associated inherited retinal dystrophies caused by novel and recurrent variants using exome sequencing
Genotoxicity of cisplatin and carboplatin in cultured human lymphocytes: a comparative study
The frequency of NOTCH1 variants in T-acute lymphoblastic leukemia/lymphoma and chronic lymphocytic leukemia/small lymphocytic lymphoma among Jordanian patients
Novel CERKL variant in consanguineous Jordanian pedigrees with inherited retinal dystrophies
Novel frameshift variant in the IDUA gene underlies Mucopolysaccharidoses type I in a consanguineous Yemeni pedigree
Missing publications? Search for publications with a matching author name.