Ectrodactyly and proximal/intermediate interstitial deletion 7q
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference38 articles.
1. Cat-like cry and mental retardation owing to 7q interstitial deletion (7q22 leads to 7q32).
2. EC syndrome In a girl with paracentric inversion (7)(q22A;q36.3)
3. Clinico-pathological conference: A preterm infant with multiple congenital anomalies
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1. Osteogenesis Imperfecta and Split Foot Malformation due to 7q21.2q21.3 Deletion Including COL1A2, DLX5/6 Genes: Review of the Literature;Journal of Pediatric Genetics;2021-11-02
2. 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
3. Duplication of 10q24 locus: broadening the clinical and radiological spectrum;European Journal of Human Genetics;2019-01-08
4. 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
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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