Case Reports
Familial Y/22 translocation in a woman
- PMID: 571896
Item in Clipboard
Case Reports
Familial Y/22 translocation in a woman
J Genet Hum.
1978 Dec.
Abstract
A phenotypically normal 35-year-old woman who had a malformed fetus was found to have a Y/22 translocation. One brother as well as a sister and her three children also have the Y/22 chromosome while another sister lacks it. The problem raised by the presence of this translocated chromosome for genetic counseling, especially for prenatal diagnosis, is emphasized.
Similar articles
-
[Familial translocation 22/Y and partial autosomal trisomy in a young girl].J Genet Hum. 1979 Mar;27(1):45-51. J Genet Hum. 1979. PMID: 573310 French.
-
[Reciprocal translocation at the origin of a Robertsonian translocation 15;22 by the loss of a metacentric chromosome. Genetic counseling].J Genet Hum. 1984 Dec;32(5):363-8. J Genet Hum. 1984. PMID: 6527132 French.
-
Ring chromosome 21 in a normal female.Ann Genet. 1984;27(2):126-8. Ann Genet. 1984. PMID: 6331791
-
Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literature.Prenat Diagn. 1999 Mar;19(3):282-6. Prenat Diagn. 1999. PMID: 10210132 Review.
-
[Numerical and structural aberrations of human Y chromosome].Pol Tyg Lek. 1980 Apr 14;35(15):543-6. Pol Tyg Lek. 1980. PMID: 6995959 Review. Polish. No abstract available.
Cited by
-
Localisation of male determining factors in man: a thorough review of structural anomalies of the Y chromosome.J Med Genet. 1981 Jun;18(3):161-95. doi: 10.1136/jmg.18.3.161. J Med Genet. 1981. PMID: 7017147 Free PMC article. Review.