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PMID: 5046906 Published · ppublish English Journal Article

Short arm deletion of chromosome 14.

Humangenetik ·Vol. 15 ·No. 1 ·1972-00-00 ·Pages 33-8

Emerit I, Noel B, Thiriet M, Loubon M, Quack B

Abstract

暂无摘要

MeSH Terms
Autoradiography Blood Group Antigens Child Chromosome Aberrations Chromosome Disorders Chromosomes, Human, 13-15 Chromosomes, Human, 21-22 and Y Cytogenetics Epilepsy Female Humans Intellectual Disability Karyotyping Male Pedigree Phenotype
Chemicals
Blood Group Antigens
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Emerit I
Noel B
Thiriet M
Loubon M
Quack B
References (9)
9 references, click to expand
  1. Exclusion of marker genes from the short arm of the human chromosome D1 by deletion mapping.
    Hereditas. 1969;62(1):116-30 PMID: 5399209
  2. Haptoglobin: a locus on the D1 chromosome?
    Am J Hum Genet. 1967 May;19(3 Pt 2):393-8 PMID: 6026932
  3. 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
  4. DNA REPLICATION PATTERNS OF HUMAN CHROMOSOMES.
    Cytogenetics. 1963;2:175-93 PMID: 14101501
  5. Atypical acrocentric chromosomes in Negro and Caucasian Mongols.
    Am J Hum Genet. 1967 Mar;19(2):162-73 PMID: 4225661
  6. [A short arm deletion of chromosome 13].
    Ann Genet. 1968 Sep;11(3):184-6 PMID: 5304619
  7. [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
  8. [Studies of the DNA replication pattern of the chromosome groups 4-5, 13-15 and 21-22 in invitro cultured human leukocytes].
    Humangenetik. 1966;2(3):246-61 PMID: 5984968
  9. RESEARCH ON PREMATURE INFANTS--SOME PERSPECTIVES.
    Pediatrics. 1963 Sep;32:319-25 PMID: 14063509
Article Info
Journal
Humangenetik
Abbr.
Humangenetik
ISSN
0018-7348
Published
1972-00-00
Pages
33-8
Language
English
Region
Germany
NLM ID
7607154
Subset
IM
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