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Author Details
Full Name
Zerin Hyder
Affiliation
University of Manchester
ORCID
Career Start Year
2017
Papers
8
H Index
5
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
34612517
Biallelic TMEM260 variants cause truncus arteriosus, with or without renal defects.
Clin Genet
2022
32917767
Constitutional de novo deletion CNV encompassing <i>REST</i> predisposes to diffuse hyperplastic perilobar nephroblastomatosis (HPLN).
J Med Genet
2021
33603162
ERBB4 exonic deletions on chromosome 2q34 in patients with intellectual disability or epilepsy.
Eur J Hum Genet
2021
34758253
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.
N Engl J Med
2021
33993487
Isolated- and Beckwith-Wiedemann syndrome related- lateralised overgrowth (hemihypertrophy): Clinical and molecular correlations in 94 individuals.
Clin Genet
2021
32045981
Risk of Contralateral Breast Cancer in Women with and without Pathogenic Variants in <i>BRCA1, BRCA2</i>, and <i>TP53</i> Genes in Women with Very Early-Onset (<36 Years) Breast Cancer.
Cancers (Basel)
2020
31045593
Chromosome 1q31.2q32.1 deletion in an adult male with intellectual disability, dysmorphic features and obesity.
Clin Dysmorphol
2019
28166087
Genitourinary malformations: an under-recognized feature of ectrodactyly, ectodermal dysplasia and cleft lip/palate syndrome.
Clin Dysmorphol
2017
1 - 8 of 8
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