Fusion of the short arms of one X chromosome in a patient with gonadal dysgenesis.

Humangenetik ·Vol. 24 ·No. 2 ·1974-00-00 ·Pages 159-60

Ruthner U, Golob E

Abstract

暂无摘要

MeSH Terms

Adult Cell Division Chromatids Chromosome Aberrations Female Heterochromatin Humans Karyotyping Ovum/growth & development Sex Chromosomes Turner Syndrome/genetics

Chemicals

Heterochromatin

Authors & Affiliations

2 authors, click to expand affiliations / ORCID

Ruthner U

Golob E

References (1)

1 references, click to expand

An abnormal large human chromosome identified as an end-to-end fusion of two X's by combined results of the new banding techniques and microdensitometry.
Clin Genet. 1972;3(5):388-95 PMID: 4117330

Article Info

Journal

Humangenetik

Abbr.

Humangenetik

ISSN

0018-7348

DOI

10.1007/BF00283775

Published

1974-00-00

Pages

159-60

Language

English

Region

Germany

NLM ID

7607154

Subset

External Links

PubMed source DOI: 10.1007/BF00283775

Analysis Services

Fusion of the short arms of one X chromosome in a patient with gonadal dysgenesis.

Contact

WeChat Official Account