Severe clinical phenotype due to an interstitial deletion of the short arm of chromosome 1: A brief review
- 8 August 1997
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 71 (2) , 189-193
- https://doi.org/10.1002/(sici)1096-8628(19970808)71:2<189::aid-ajmg13>3.0.co;2-a
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Role of Ploidy, Chromosome 1p, and Schwann Cells in the Maturation of NeuroblastomaNew England Journal of Medicine, 1996
- Developmental delay and dysmorphic features associated with a previously undescribed deletion on chromosome 1.Journal of Medical Genetics, 1995
- Deletion of chromosome arm 1p in a merkel cell carcinoma (MCC)Genes, Chromosomes and Cancer, 1994
- Interstitial deletion in chromosome 1: Assignment of the breakpointsAmerican Journal of Medical Genetics, 1993
- Interstitial deletion of the short arm of chromosome 1 (46XY), del(1)(p13p22.3)American Journal of Medical Genetics, 1992
- Two cases of interstitial deletion 1p.Journal of Medical Genetics, 1991
- Deletion of chromosome 1p: a short reviewClinical Genetics, 1990
- Interstitial deletion 1p in a 30 year old woman.Journal of Medical Genetics, 1987
- De novo interstitial deletion del(1)(p21p32).Journal of Medical Genetics, 1979
- A large deletion of chromosome no. 1 (46,XY,1?--).Journal of Medical Genetics, 1968