Triple structural mosaicism of chromosome 18 in a child with MR/MCA syndrome and abnormal skin pigmentation.

Author:

Bocian E,Mazurczak T,Bulawa E,Stanczak H,Rowicka G

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference9 articles.

1. Hypomelanosis of Ito: a manifestation of mosaicism or chimerism;Donnai D, Read AP, McKeown C, Andrews T;J Med Genet,1988

2. Invited editorial comment: pigmentary dysplasia, hypomelanosis of Ito, and genetic mosaicism;Flannery, D.;Am J Med Genet,1990

3. Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism;Thomas, I.T.; Frias, J.L.; Cantu, E.S.; Lafer, C.Z.; Flannery, D.B.; Graham, J.G.;Am J Hum Genet,1989

4. Unusual cytogenetic mosaicism involving chromosome 14 abnormalities in a child with an MR/MCA syndrome and abnormal pigmentation;Cantu, E.; Thomas, I.; Frias, J.;Clin Genet,1989

5. Trisomy 14 mosaicism with t(14; 15)(qll; pll) in offspring of a balanced translocation carrier mother;Fujimoto, A.; Lin, M.; Korula, S.; Wilson, M.;Am J Hum Genet,1985

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