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PMID: 4135219 Published · ppublish English Journal Article

Frequency of deletion of short arm satellites in acrocentric chromosomes.

Journal of medical genetics ·Vol. 11 ·No. 2 ·1974-06-00 ·Pages 177-80

Nielsen J, Friedrich U, Hreidarsson AB

Abstract

暂无摘要

MeSH Terms
Adolescent Adult Cell Division Chromosome Aberrations Chromosomes, Human, 13-15 Chromosomes, Human, 21-22 and Y Denmark Female Genetics, Population Hospitals, Psychiatric Humans Infant, Newborn Karyotyping Male Pedigree Personality Disorders/genetics Prisons Staining and Labeling
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Nielsen J
Friedrich U
Hreidarsson A B
References (12)
12 references, click to expand
  1. [Deletion of the short arm of a 13-15 chromosome, hypertelorism and Hp0 haptoglobin phenotype in the same family].
    Ann Genet. 1966 Jun;9(2):80-5 PMID: 5296303
  2. Atypical acrocentric chromosomes in Negro and Caucasian Mongols.
    Am J Hum Genet. 1967 Mar;19(2):162-73 PMID: 4225661
  3. Haptoglobin: a locus on the D1 chromosome?
    Am J Hum Genet. 1967 May;19(3 Pt 2):393-8 PMID: 6026932
  4. Unilateral fixation of the ossicular chain associated with G-group chromosome deletion.
    Can Med Assoc J. 1967 May 27;96(21):1405-7 PMID: 6026993
  5. Familial deletion of the short arm of the D1-chromosome (46, XX, 13 p-) not associated with loss of haptoglobin or catalase activity.
    Clin Pediatr (Phila). 1969 Aug;8(8):453-8 PMID: 5797429
  6. Familial occurrence of a short arm deletion of a G-group chromosome.
    Jinrui Idengaku Zasshi. 1969 Sep;14(2):140-4 PMID: 5392344
  7. The G deletion syndromes.
    J Pediatr. 1970 Oct;77(4):658-63 PMID: 5454712
  8. Exclusion of marker genes from the short arm of the human chromosome D1 by deletion mapping.
    Hereditas. 1969;62(1):116-30 PMID: 5399209
  9. Group G deletion syndromes.
    J Med Genet. 1971 Sep;8(3):341-5 PMID: 5097140
  10. Chromosome studies in a neonatal population.
    Can Med Assoc J. 1972 Apr 8;106(7):776-9 PMID: 4259580
  11. Short arm deletion of chromosome 14.
    Humangenetik. 1972;15(1):33-8 PMID: 5046906
  12. FAMILIAL VARIANT AUTOSOMES: NEW HUMAN CYTOGENETIC MARKERS.
    Bull Johns Hopkins Hosp. 1965 Jun;116:396-402 PMID: 14300779
Article Info
Journal
Journal of medical genetics
Abbr.
J Med Genet
ISSN
0022-2593
DOI
10.1136/jmg.11.2.177
Published
1974-06-00
Pages
177-80
Language
English
Region
England
NLM ID
2985087R
PMCID
PMC1013115
Subset
IM
External Links
PubMed source DOI: 10.1136/jmg.11.2.177 PMC Full Text View journal details
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