Bilateral complete radioulnar synostosis associated with ectrodactyly and sensorineural hearing loss: a variant of SHFM1
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference21 articles.
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3. Split hand/split foot malformation, deafness, and mental retardation with a complex cytogenetic rearrangement involving 7q21.3;Ignatius;J Med Genet,1996
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1. Genetic cold cases: lessons from solving complex congenital limb disorders;Genes & Development;2023-03-29
2. Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani-Lenz-like non-syndromic oligosyndactyly;Journal of Medical Genetics;2010-07-07
3. 22q11 Deletion Syndrome and Limb Anomalies: Report on Two Brazilian Patients;The Cleft Palate-Craniofacial Journal;2008-09
4. The common inversion of the Williams–Beuren syndrome region at 7q11.23 does not cause clinical symptoms;American Journal of Medical Genetics Part A;2008-07-15
5. Genotype–phenotype correlations in mapped split hand foot malformation (SHFM) patients;American Journal of Medical Genetics Part A;2006
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