Y chromosome heterochromatin variation detected at prenatal diagnosis [3]

Prenatal Diagnosis

Volumn 25, Issue 11, 2005, Pages 1062-1063

  Cotter, Philip D ^a,b   Norton, Mary E ^b  

^a CHILDREN S HOSPITAL OAKLAND   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AMNIOCENTESIS; CASE REPORT; CHROMOSOME ABERRATION; CHROMOSOME SIZE; CHROMOSOME TRANSLOCATION; CHROMOSOME VARIANT; FEMALE; FETUS; FETUS ECHOGRAPHY; HETEROCHROMATIN; HUMAN; IN SITU HYBRIDIZATION; KARYOTYPE 46,XY; LETTER; MOSAICISM; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; Y CHROMOSOME;

ADULT; CHROMOSOMES, HUMAN, Y; FEMALE; HETEROCHROMATIN; HUMANS; MALE; MOSAICISM; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 28544435210     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.1280     Document Type: Letter

References (5)

1. Akkari Y, Lawce H, Kelson S, et al. 2005. Y chromosome heterochromatin of differing lengths in two cell populations of the same individual. Prenat Diagn 25: 304-306.
2. Holden JJ, Ridgway P, Smith A. 1986. A possible fragile-site at Yq 12: case report and possible relevance to de novo structural rearrangements of the Y-chromosome. Am J Med Genet 23: 545-555.
3. Ma K, Mallidis C, Bhasin S. 2000. The role of Y chromosome deletions in male infertility. Eur J Endocrinol 142: 418-430.
4. Nazarenko SA, Nazarenko LP, Baranova VA. 1987. Intra-individual polymorphism of human Y chromosome as a result of deletion in the heterochromatin region. Genetika 23: 918-921.
5. Wahlstrom J, Kyllerman M, Hansson A, Taranger J. 1985. Unequal mitotic sister chromatid exchange and different length of Y chromosomes. Hum Genet 70: 186-188.