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PMID: 4140834 Published · ppublish English Journal Article

Malformative syndrome with ring chromosome 13.

Humangenetik ·Vol. 24 ·No. 3 ·1974-00-00 ·Pages 235-40

Fryns JP, Deoover J, Van den Berghe H

Abstract

暂无摘要

MeSH Terms
Abnormalities, Multiple/genetics Adolescent Chromosome Aberrations/genetics Chromosome Disorders Chromosomes, Human, 13-15 Craniofacial Dysostosis/genetics Fibroblasts/ultrastructure Humans Intellectual Disability/genetics Karyotyping Lymphocytes/ultrastructure Male Microcephaly/genetics Microphthalmos/genetics Staining and Labeling
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Fryns J P
Deoover J
Van den Berghe H
References (3)
3 references, click to expand
  1. Retinoblastoma and D-chromosome deletions.
    Am J Hum Genet. 1973 Jan;25(1):57-61 PMID: 4119334
  2. Ring chromosome D (13) associated with multiple congenital malformations.
    Ann Genet. 1973 Sep;16(3):157-66 PMID: 4543204
  3. [Ring chromosome D13-case history and survey (author's transl)].
    Klin Padiatr. 1973 May;185(3):192-7 PMID: 4795573
Article Info
Journal
Humangenetik
Abbr.
Humangenetik
ISSN
0018-7348
DOI
10.1007/BF00283592
Published
1974-00-00
Pages
235-40
Language
English
Region
Germany
NLM ID
7607154
Subset
IM
External Links
PubMed source DOI: 10.1007/BF00283592
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