Molecular studies of an X;Y translocation chromosome in a woman with deletion of the pseudoautosomal region but normal height
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1997.tb02486.x/fullpdf
Reference28 articles.
1. Y-to-X chromosome translocation observed in two generations;Akesson;Hum Genet,1980
2. X:Y translocation in an adolescent mentally normal phenotypic male with features of hypogonadism;Bernstein;J Med Genet,1980
3. Genetic evidence equating SRY and the testis determining factor;Berta;Nature,1990
4. The human Y chromosome: overlapping DNA clones spanning the euchromistic region;Foote;Science,1992
5. Molecular diagnosis of Turner's syndrome;Gicquel;J Med Genet,1992
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1. Fate of SRY, PABY, DYS1, DYZ3 and DYZ1 loci in Indian patients harbouring sex chromosomal anomalies;MHR: Basic science of reproductive medicine;2005-02-01
2. Genomics of the human Y-chromosome;Gene;2003-12
3. SHOX: A Geneticist’s View;The Journal of Clinical Endocrinology & Metabolism;2002-04-01
4. Brachytelephalangic dwarfism due to the loss of ARSE and SHOX genes resulting from an X;Y translocation;Clinical Genetics;2001-02
5. Atypical phenotype in a female with a large Xp deletion;American Journal of Medical Genetics;2001
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