Frequency of 9qh+ and risk of chromosome aberrations in the progeny of individuals with 9qh+
- 1 January 1974
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 21 (3) , 211-216
- https://doi.org/10.1007/bf00279014
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Banding characteristics of paracentric marker constrictions in human chromosomesHereditas, 2009
- A familial variant of chromosome 9.Journal of Medical Genetics, 1971
- Localization of heterochromatin in human chromosomesCytogenetic and Genome Research, 1971
- Cytogenetics of Down’s Syndrome (Mongolism) I. Data on a Consecutive Series of Patients Referred for Genetic Counselling and DiagnosisCytogenetic and Genome Research, 1965