Paper Details

Paper Title

Phenotypic and mutational spectrum of ROR2-related Robinow syndrome.

Paper Journal Title

Hum Mutat

Paper Citation Count

Paper Publication Year

2022

Bio Mention

ROR2, ROR2 variants, Robinow syndrome, WNT, abnormality of the nasal tip, brachydactyly, craniofacial dysmorphisms, disproportionate-limb short stature, exonic deletion variant alleles, exonic deletions, genes/, genital hypoplasia, hypertelorism, loci, mesomelic limb shortening, patients, prominent forehead, short nose, short stature, skeletal defects

Mesh Descriptor

Author Name	Affiliation
H??lya Kayserili	Koc University
Zeynep Coban Akdemir	Baylor College of Medicine
Zeynep Coban Akdemir	School of Public Health
Shalini N Jhangiani	Baylor College of Medicine
Donna M Muzny	Baylor College of Medicine
Donna M Muzny	Baylor College of Medicine
Richard A Gibbs	Baylor College of Medicine
Richard A Gibbs	Baylor College of Medicine
Han G Brunner	Radboud University Nijmegen Medical Centre
Vernon R Sutton	Baylor College of Medicine
Vernon R Sutton	Texas Children's Hospital
James R Lupski	Baylor College of Medicine
James R Lupski	Baylor College of Medicine
James R Lupski	Texas Children's Hospital
James R Lupski	Baylor College of Medicine
James R Lupski	Baylor College of Medicine
James R Lupski	Baylor College of Medicine
James R Lupski	Texas Children's Hospital
James R Lupski	Baylor College of Medicine

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