Submicroscopic deletions at 16p13.3 in Rubinstein-Taybi syndrome: frequency and clinical manifestations in a North American population.

Author:

Wallerstein R,Anderson C E,Hay B,Gupta P,Gibas L,Ansari K,Cowchock F S,Weinblatt V,Reid C,Levitas A,Jackson L

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference15 articles.

1. Broad thumbs and toes and facial abnormalities. A possible mental retardation syndrome;Rubinstein, J.H.; Taybi, H.;Am 7 Dis Child,1963

2. Apparent dominant transmission of the Rubinstein-Taybi syndrome;Marion, R.W.; Garcia, D.M.; Karasik, J.B.;Amn_T Med Genet,1993

3. Rubinstein-Taybi syndrome in a mother and son;Hennekam, R.C.M.; Lommen, E.J.P.; Strengers, J.C.M.; Van Spijker, H.G.; Jansen-Kokx, T.M.G.,1989

4. Tentative assignment of a locus for Rubinstein-Taybi syndrome to 16fpl3.3 by a de novo reciprocal translocation t(7; 16)(q34; p13.3);Tommerup, N.; Van der Hagen, C.B.; Heiberg, A.;Cytogenet Cell Genet,1991

5. Rubinstein-Taybi syndrome with de novo reciprocal translocation t(2; 16)(pl3.3; pl3.3);Imaizumi, K.; Kuroki, Y.;Am.7 Med Genet,1991

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