Robin sequence and a deficiency of the left forearm in a girl with a deletion of chromosome 4q33-qter
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference9 articles.
1. Oromandibular Limb Hypogenesis Syndromes
2. Del(4)(q33----qter): another case report of a child with mild dysmorphism.
3. A terminal deletion of the long arm of chromosome 4 [46,XX,del(4)(q33)] in an infant with phenotypic features of Williams syndrome.
4. Interstitial and terminal deletions of the long arm of chromosome 4: Further delineation of phenotypes
5. Deletions of different segments of the long arm of chromosome 4
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1. Clinical comparison between terminal and interstitial 4q deletion in two unrelated children;2022-10-10
2. Clinical, cytogenetic, and molecular outcomes in a series of 66 patients with Pierre Robin sequence and literature review: 22q11.2 deletion is less common than other chromosomal anomalies;American Journal of Medical Genetics Part A;2016-01-12
3. Bilateral absence of the ulna in 4q terminal deletion syndrome;Clinical Dysmorphology;2015-07
4. Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature;BMC Medical Genetics;2014-06-25
5. 2q34-qter duplication and 4q34.2-qter deletion in a patient with developmental delay;European Journal of Medical Genetics;2012-03
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