The Rubinstein-Taybi Syndrome: chromosomal studies
- PMID: 4735812
- PMCID: PMC1762544
The Rubinstein-Taybi Syndrome: chromosomal studies
Similar articles
-
The Bubinstein-Taybi syndrome: familial and dermatoglyphic data.Am J Hum Genet. 1973 May;25(3):225-9. Am J Hum Genet. 1973. PMID: 4704855 Free PMC article. No abstract available.
-
[Rubinstein-Taybi syndrome. (2 cases studied also from a chromosomal point of view)].Haematologica. 1969;54(12):899-919. Haematologica. 1969. PMID: 4993256 Italian. No abstract available.
-
[Rubinstein-Taybi syndrome. Discussion of incomplete and familial forms].Pediatrie. 1970 Jan-Feb;25(1):89-102. Pediatrie. 1970. PMID: 5416723 French. No abstract available.
-
Terminal deletion of the long arm of chromosome 4 in a mother and two sons.Clin Genet. 1996 Dec;50(6):538-40. doi: 10.1111/j.1399-0004.1996.tb02733.x. Clin Genet. 1996. PMID: 9147894 Review.
-
Rubinstein-Taybi syndrome.J Med Genet. 1987 Sep;24(9):562-6. doi: 10.1136/jmg.24.9.562. J Med Genet. 1987. PMID: 3312608 Free PMC article. Review. No abstract available.
Cited by
-
Partial trisomy 13: karyotype 46,XY,-6, plus t(13q,6q).Humangenetik. 1974 Jan 22;21(1):47-54. doi: 10.1007/BF00278564. Humangenetik. 1974. PMID: 4837512 No abstract available.
References
MeSH terms
LinkOut - more resources
Full Text Sources