Atypical gonadal dysgenesis: the role of Yq in determining phenotype and malignancy risk
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1984.tb01987.x/fullpdf
Reference17 articles.
1. Isochromosome Y(46,X, i(Yq)) and female phenotype;Böök;Clin. Genet,1973
2. Familial Y/22 transloc-ation in a woman;Chieri;J. Genet. Hum.,1978
3. True hermaphroditism: clinical description and proposed function for long arm of Y chromosome;Donahoe;J. Pediatr. Surg.,1978
4. Isochromosome for the long arm of Y chromosome in a patient with Turner's Syndrome and sex chromosome mosaicism 45,X/46,Xyqi;Ferguson-Smith;J. Med. Genet,1969
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1. Genomic distribution of 5‘ TTCCA 3’ repeat motif and its diagnostic potential in human Y-chromosome-related anomalies;Clinical Genetics;2008-06-28
2. Gonadoblastoma and Y-chromosome fluorescence;Clinical Genetics;2008-04-23
3. Phenotype/Karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases;American Journal of Medical Genetics;1994-11-01
4. Three cases of 45,X/46,XYnf mosaicism;Human Genetics;1987-06
5. Abnormal sexual differentiation and neoplasia;Cancer Genetics and Cytogenetics;1987-04
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