Interstitial long-arm deletion of chromosome 7 and ectrodactyly
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference23 articles.
1. Cat-like cry and mental retardation owing to 7q interstitial deletion (7q22 leads to 7q32).
2. Clinical, chromosomal and enzymatic studies in four cases of rearrangements of chromosome 7*
3. Partial monosomy 7 with interstitial deletions in two infants with differing congenital abnormalities.
Cited by 44 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Deletion 7q21.2-q22.1 in a case with split hand-split foot malformation, sensorineural hearing loss and intellectual disability: Phenotype subtypes and the correlation with genotypes;European Journal of Medical Genetics;2019-12
2. Interstitial deletion of 7q22.1q31.1 in a boy with structural brain abnormality, cardiac defect, developmental delay, and dysmorphic features;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2016-04-20
3. Delineation of a de novo 7q21.3q31.1 Deletion by CGH-SNP Arrays in a Girl with Multiple Congenital Anomalies Including Severe Glaucoma;Molecular Syndromology;2013
4. The Dysostoses;Emery and Rimoin's Principles and Practice of Medical Genetics;2013
5. Identification of a novelDLX5mutation in a family with autosomal recessive split hand and foot malformation;Journal of Medical Genetics;2011-11-25
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