Familial transmission of a duplication-deficiency X chromosome associated with partial Turner syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1995.tb04117.x/fullpdf
Reference18 articles.
1. Partial Turner's syndrome in four girls with Xq duplication and Xp deficiency;Bjerglund;Hum Genet,1982
2. Determining the origin of human X isochromosomes by use of DNA sequence polymorphism and detection of an apparent i(Xq) with Xp sequences;Callen;Hum Genet,1987
3. Fertility in patients with X chromosome deletions;Fryns;Clin Genet,1982
4. The gene responsible for X-linked cleft palate (CPX) in a British Columbia native family kindred is localized between PGK1 and DXYS1;Gorski;Am J Med Genet,1992
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1. Apparent Neotelomere in a 46,X,del(X)(qter→p11.2:)/46,X,rea(X)(qter→p11.2::q21.2→qter) Novel Mosaicism: Review of 34 Females with a Recombinant-Like dup(Xq) Chromosome;Genetic Testing and Molecular Biomarkers;2011-10
2. Successful pregnancy with preimplantation genetic diagnosis in a woman with mosaic Turner syndrome;Fertility and Sterility;2011-04
3. Recombinant X chromosome in a prenatal diagnosis;Cytogenetic and Genome Research;2006
4. Health Supervision for Children With Turner Syndrome;Pediatrics;2003-03-01
5. Molecular and cytogenetic analysis of familial Xp deletions;American Journal of Medical Genetics;2000
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