Interstitial deletion in the long arms of chromosome 1: 46,XY,del(1)(pter leads to q22::q25 leads to qter).
Open Access
- 1 December 1980
- journal article
- case report
- Published by BMJ in Journal of Medical Genetics
- Vol. 17 (6) , 483-486
- https://doi.org/10.1136/jmg.17.6.483
Abstract
A child was brought to us with multiple anomalies. On examination we found an interstitial deletion in the long arms of chromosome 1. We studied genetic and chromosome markers, comparing our clinical and cytogenetic findings with other reported cases of chromosome 1 interstitial deletion.Keywords
This publication has 11 references indexed in Scilit:
- Deletion in the long arm of chromosome 1 from a subject with multiple congenital anomaliesCytogenetic and Genome Research, 1978
- Four further families informative for 1q and the Duffy blood groupCytogenetic and Genome Research, 1978
- Assignment of a molecular form of UDP glucose pyrophosphorylase (UGPP2) to chromosome 2 in manCytogenetic and Genome Research, 1978
- Partial Deletion of 1q, Following a Pericentric Inversion, in a Boy with Multiple Minor Morphologic Anomalies and Mental RetardationActa geneticae medicae et gemellologiae, 1977
- Partial monosomy or trisomy resulting from crossing over within a rearranged chromosome 1Clinical Genetics, 1976
- PRIMARY HYPOTHYROIDISM, GROWTH HORMONE DEFICIENCY AND CONGENITAL MALFORMATIONS IN A CHILD WITH THE KARYOTYPE 46, XY, del(l)(q25q32)Acta Paediatrica, 1976
- [De novo interstitial deletion Del (1) (q24 q32.1) in a malformed child].1974
- Centromere staining at meiosis in manHuman Genetics, 1973
- A RAPID BANDING TECHNIQUE FOR HUMAN CHROMOSOMESThe Lancet, 1971
- Identification of human chromosomes by DNA-binding fluorescent agentsChromosoma, 1970