Parental origin of the X chromosome, X chromosome mosaicism and screening for “hidden” Y chromosome in 45,X Turner syndrome ascertained cytogenetically

Author:

Larsen Torben,Gravholt Claus Højbjerg,Tillebeck Annette,Larsen Hanne,Jensen Marianne Bryder,Nielsen Johannes,Friedrich Ursula

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference38 articles.

1. Dinucleotide repeat polymorphism at the MAOA locus;Black;Nucleic Acids Res,1991

2. Possible role of imprinting in the Turner phenotype;Chu;J Med Genet,1994

3. Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa;Coleman;Am J Hum Genet,1990

4. Molecular genetics of Turner's syndrome;Connor;Acta Paediatr Scand Suppl,1989

5. Repeated sequence specific to human males;Cooke;Nature,1976

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1. Recognition of the Y chromosome in Turner syndrome using peripheral blood or oral mucosa tissue;Annals of Pediatric Endocrinology & Metabolism;2021-12-31

2. Detection of the SRY gene in patients with Turner Syndrome;Journal of Gynecology Obstetrics and Human Reproduction;2019-04

3. Genetic Defects of Female Sexual Differentiation;Hormones, Brain and Behavior;2017

4. Buccal cell FISH and blood PCR-Y detect high rates of X chromosomal mosaicism and Y chromosomal derivatives in patients with Turner syndrome;European Journal of Medical Genetics;2013-09

5. Turner Syndrome;Atlas of Genetic Diagnosis and Counseling;2012

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