Genetic and molecular analysis of a new unbalanced X;18 rearrangement: localization of the diminished ovarian reserve disease locus in the distal Xq POF1 region

Author:

Fusco Francesca,Paciolla Mariateresa,Chen Emily,Li Xu,Genesio Rita,Conti Anna,Jones Julie,Poeta Loredana,Lioi Maria Brigida,Ursini Matilde Valeria,Miano Maria Giuseppina

Publisher

Oxford University Press (OUP)

Subject

Obstetrics and Gynecology,Rehabilitation,Reproductive Medicine

Reference59 articles.

1. Array comparative genomic hybridization profiling analysis reveals deoxyribonucleic acid copy number variations associated with premature ovarian failure;Aboura;J Clin Endocrinol Metab,2009

2. Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation;Allen;Am J Hum Genet,1992

3. Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation;Auber;Mol Cytogenet,2009

4. Autoimmune diseases in a Danish cohort of 4,866 carriers of constitutional structural chromosomal rearrangements;Bache;Arthritis Rheum,2007

5. Molecular cytogenetic definition of a translocation t(X;15) associated with premature ovarian failure;Bertini;Fertil Steril,2010

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