Home LiteratureArticle Details
PMID: 924439 Published · ppublish English Case Reports Journal Article

Yq deletion, aspermia, and short stature.

Human genetics ·Vol. 39 ·No. 1 ·1977-11-02 ·Pages 117-22

Yunis E, García-Conti FL, de Caballero OM, Giraldo A

Abstract

A large Yq deletion involving both the fluorescent and part of the non-fluorescent segment in a 36-year-old phenotypic normal male is presented. His short stature and aspermia gives strong support, after a complete review of the literature, to the existence of factors involved in the control of both characteristics in the non-fluorescent segment of the long arm of chromosome Y, distally within band 11.

MeSH Terms
Adult Biopsy Chromosome Deletion Growth Disorders/diagnosis Humans Infertility, Male/diagnosis Karyotyping Male Phenotype Sex Chromosomes Testis/pathology Y Chromosome
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Yunis E
García-Conti F L
de Caballero O M
Giraldo A
References (18)
18 references, click to expand
  1. New technique for distinguishing between human chromosomes.
    Nat New Biol. 1971 Jul 7;232(27):31-2 PMID: 4105244
  2. Probable long-arm deletion of Y chromosome in boy of short stature.
    Lancet. 1973 Mar 17;1(7803):608 PMID: 4120673
  3. Length variation in the quinacrine-binding segment of human Y chromosomes of different sizes.
    Cytogenetics. 1971;10(3):190-8 PMID: 5156693
  4. Deletion of the long arms of the Y chromosome with normal male development and intelligence.
    J Med Genet. 1974 Jun;11(2):208-11 PMID: 4841088
  5. Structural abnormalities of the Y chromosome in man.
    Nature. 1966 Apr 23;210(5034):352-4 PMID: 5963227
  6. Meiotic studies on a subfertile patient with a ring Y chromosome.
    Cytogenetics. 1971;10(4):295-304 PMID: 5127018
  7. Communications and commentaries: A 46,XYq- male with aspermia.
    Fertil Steril. 1973 Oct;24(10):811-3 PMID: 4742003
  8. A strongly fluorescing abnormal chromosome in a malformed child.
    Humangenetik. 1971;12(1):64-6 PMID: 4104180
  9. Minute Y chromosome.
    Ann Genet. 1971 Jun;14(2):145-8 PMID: 5314803
  10. Isochromosome Y (46,X,i(Yq)) and female phenotype.
    Clin Genet. 1973;4(5):410-4 PMID: 4751309
  11. Normal male development with Y chromosome long arm deletion (Yq-).
    J Med Genet. 1972 Sep;9(3):373-7 PMID: 5079110
  12. A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities.
    Clin Genet. 1975 Oct;8(4):223-43 PMID: 1183067
  13. Localization of male determining factor on short arm of Y chromosome. Case report of a baby with 46, x, t (Yp+;14q-).
    Clin Genet. 1972;3(5):381-7 PMID: 4673472
  14. Ring Y chromosome: 45,X/46,Xr(Y) chromosome mosaicism in a phenotypically normal male with azoospermia.
    Hum Genet. 1976 Sep 10;34(1):99-102 PMID: 965013
  15. Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm.
    Hum Genet. 1976 Oct 28;34(2):119-24 PMID: 1002136
  16. Abnormalities of human sex chromosomes. I. A ring Y without mosaiciam.
    Ann Genet. 1973 Dec;16(4):225-31 PMID: 4544085
  17. Deletion of Y chromosome in a family with muscular dystrophy and hypospadias.
    Br Med J. 1962 Feb 3;1(5274):291-4 PMID: 14477078
  18. X"Y"-XO MOSAICISM IN A PHENOTYPIC INTERSEX; REPORT OF A CASE.
    Am J Clin Pathol. 1965 Mar;43:251-5 PMID: 14270968
Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
Published
1977-11-02
Pages
117-22
Language
English
Region
Germany
NLM ID
7613873
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com