Sex dependent transmission of Beckwith-Wiedemann syndrome associated with a reciprocal translocation t(9;11)(p11.2;p15.5).

Author:

Tommerup N,Brandt C A,Pedersen S,Bolund L,Kamper J

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference21 articles.

1. Lymphoblastoid cell lines from the two translocation carriers;1812-89L/1813-89L

2. Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature;Pettenati, M.J.; Haines, J.L.; Higgins, R.R.; Wappner, R.S.; Palmer, C.G.; Weaver, D.D.;Hum Genet,1986

3. Wiedemann-Beckwith syndrome: autosomal-dominant inheritance in a family;Best, L.G.; Hoekstra, R.E.

4. The Wiedemann-Beckwith syndrome: pedigree studies on five families with evidence for autosomal dominant inheritance with variable expressivity;Niikawa, N.; Takahashi, Ishikiriyama;Am J7 Med Genet,1986

5. Dominant inheritance of Wiedemann-Beckwith syndrome: further evidence for transmission of unstable premutation through carrier women;Aleck, K.A.; Hadro, T.A.;Am I Med Genet,1989

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