Terminal deletion of the long arm of chromosome 1 in a malformed newborn
- 1 January 1978
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 42 (3), 333-337
- https://doi.org/10.1007/bf00291316
Abstract
Microcephaly and craniofacial dysmorphia, cleft palate, cardiac malformation, and hypospadias are observed in a child with 46,XY,del (1)(q42).This publication has 7 references indexed in Scilit:
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- PRIMARY HYPOTHYROIDISM, GROWTH HORMONE DEFICIENCY AND CONGENITAL MALFORMATIONS IN A CHILD WITH THE KARYOTYPE 46, XY, del(l)(q25q32)Acta Paediatrica, 1976
- Terminal (1)(q43) long-arm deletion of chromosome no. 1 in a three-year-old female.1976
- [De novo interstitial deletion Del (1) (q24 q32.1) in a malformed child].1974
- Ring-1 Chromosome, Microcephalic Dwarfism, and Acute Myeloid LeukemiaArchives of Pediatrics & Adolescent Medicine, 1973
- Ring 1 chromosome and dwarfism—a possible syndromeThe Journal of Pediatrics, 1967
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