Cytogenetic and clinical characteristics of a case involving complete duplication of Xpter-->Xq13.

Author:

Jalal S M,Dahl R,Erickson L,Zimmerman D,Lindor N

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference12 articles.

1. The distribution of chromosomal genotype associated with Turner's syndrome: livebirth prevalence rates and evidence ofdiminished fetal mortality and arm deletion and those described for p arm duplication in the earlier publications. severity in genotypes associated with structural X abnormalities or mosaicism;Hook, E.B.; Warburton, D.;Hum Genet,1983

2. Isochromosome for the short arm of X: a human mosaic 45;Fitzgerald, P.H.; Donald, R.A.,1975

3. Isochromosome for short arm of X with primary amenorrhea and pituitary tumor;Keogh, E.J.; de Krester, D.M.; Fitzgerald, M.G.,1973

4. 46, XXip karyotype in a woman with normnal stature and gonadal dysgenesis without other congenital anomalies;den Berghe H, Van; JP, Fryns; F, Devos;Humangenetik,1973

5. Center for Barr body condensation on the proximal part of Xq: a hypothesis;Therman, E.; Sarto, G.E.; Patau, K.;Chromosoma (Berl),1974

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2. Prenatal Diagnosis of Sex Chromosome Abnormalities;Genetic Disorders and the Fetus;2015-11-23

3. Prenatal Diagnosis of Sex Chromosome Abnormalities;Genetic Disorders and the Fetus;2010-09-24

4. Improvement of pancytopenia and thrombocytopenia with decreasing mosaicism for isochromosome Xp;Pediatric Blood & Cancer;2009-05

5. How exhaustive are reviews in research review articles?;American Journal of Medical Genetics Part A;2007-06-01

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