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PMID: 4209591 Published · ppublish English Journal Article

A woman with multiple congenital anomalies, mental retardation and mosaicism for an unusual translocation chromosome t(6;19).

Clinical genetics ·Vol. 5 ·No. 3 ·1974-00-00 ·Pages 188-95

Pallister PD, Patau K, Inhorn SL, Opitz JM

Abstract

暂无摘要

MeSH Terms
Abnormalities, Multiple/genetics Adult Chromatids Chromosome Aberrations Chromosomes, Human, 19-20 Chromosomes, Human, 6-12 and X Chronic Disease Cleft Lip/genetics Cleft Palate/genetics Electroencephalography Epilepsy, Tonic-Clonic/genetics Female Fibroblasts/cytology Humans Intellectual Disability/genetics Karyotyping Lymphocytes/cytology Microscopy, Fluorescence Mosaicism Otitis Media/genetics Phenotype
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Pallister P D
Patau K
Inhorn S L
Opitz J M
Article Info
Journal
Clinical genetics
Abbr.
Clin Genet
ISSN
0009-9163
Published
1974-00-00
Pages
188-95
Language
English
Region
Denmark
NLM ID
0253664
Subset
IM
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