High resolution chromosome banding in the Rubinstein—Taybi syndrome
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[1] D. Ledbetter,et al. Deletions of chromosome 15 as a cause of the Prader-Willi syndrome. , 1981, The New England journal of medicine.
[2] David W. Smith,et al. Monozygotic twinning and structural defects. , 1979, The Journal of pediatrics.
[3] U. Francke,et al. Partial triplication and deletion of 13q: study of a family presenting with bilateral retinoblastomas , 1979, Clinical genetics.
[4] U. Francke,et al. Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion. , 1978, Pediatrics.
[5] A. Salisbury. The National Foundation ‐ March of Dimes , 1974, Progress in clinical and biological research.
[6] G. Carp,et al. [Rubinstein-Taybi syndrome with karyotype changes and recurrent pneumopathy]. , 1973, Ftiziologia.
[7] S. Ne. The Rubinstein-Taybi Syndrome: chromosomal studies. , 1973 .
[8] N. Simpson. The Rubinstein-Taybi Syndrome: chromosomal studies. , 1973, American Journal of Human Genetics.
[9] C. Oancea,et al. [The Rubinstein-Taybi syndrome]. , 1971, Neurologia, psihiatria, neurochirurgia.
[10] J H RUBINSTEIN,et al. Broad thumbs and toes and facial abnormalities. A possible mental retardation syndrome. , 1963, American journal of diseases of children.