A familial Xp+ chromosome, dup (Xq26.3-->qter).

Author:

Vasquez A I,Rivera H,Bobadilla L,Crolla J A

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference20 articles.

1. A new syndrome with mental retardation, short stature and an Xq duplication;Thode, A.; Partington, M.W.; Yip, M.Y.; Chapman, C.; Richardson, V.F.; Turner, G.;Am J Med Genet,1988

2. Duplications of the X chromosome in males: evidence that most parts of the X chromosome can be active in two copies;Schmidt, M.; Du Sart, D.; Kalitsis, P.;Hum Genet,1991

3. Growth hormone deficiency and empty sella syndrome in a boy with dup(X)(ql3,3--q21.2);Yokoyama, Y.; Narahara, K.; Tsuji, K.;AmJTMed Genet,1992

4. Dir dup(X)(ql3-qter) in a girl with growth retardation, microcephaly, developmental delay, seizures, and minor anomalies;Aughton, D.J.; AlSaadi, A.A.; Johnson, J.A.; Transue, D.J.; Trock, G.L.;Am J Med Genet,1993

5. Cytogenetic and molecular studies on a recombinant human X chromosome: implications for the spreading of X chromosome inactivation;Mohandas, T.; Geller, R.L.; Yen, P.H.;Proc Natl Acad Sci USA,1987

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