Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotype
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference17 articles.
1. Trisomy 9 confined to the placenta: Prenatal diagnosis and neonatal follow-up
2. Trisomy 9: Review and report of two new cases
3. Localization of the X inactivation centre on the human X chromosome in Xq13
4. Prenatal diagnosis and fetopathological findings in five fetuses with trisomy 9
5. Normal psychomotor development in a child with mosaic trisomy and pericentric inversion of chromosome 9.
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2. De novo complex intra chromosomal rearrangement after ICSI: characterisation by BACs micro array-CGH;Molecular Cytogenetics;2008-12
3. Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation;American Journal of Medical Genetics Part A;2006
4. Spreading of X-chromosome inactivation;Encyclopedia of Genetics, Genomics, Proteomics and Bioinformatics;2005-11-15
5. Molecular cytogenetic analysis of ade novobalanced X;autosome translocation: Evidence for predominant inactivation of the derivative X chromosome in a girl with multiple malformations;American Journal of Medical Genetics Part A;2003-10-21
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