[Cp trisomy: a new syndrome]
[Article in
French]
- PMID: 5315464
Item in Clipboard
[Cp trisomy: a new syndrome]
[Article in
French]
Ann Genet.
1971 Sep.
No abstract available
Similar articles
-
Familial translocation between chromosomes of groups C and D (46, T(Cq-;Dq+).Sov Genet. 1974 Jun 1;8(5):651-7. Sov Genet. 1974. PMID: 4413436 No abstract available.
-
[4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity].Ann Genet. 1970 Dec;13(4):217-32. Ann Genet. 1970. PMID: 5313386 French. No abstract available.
-
[Partial 7q trisomy].Ann Genet. 1975 Mar;18(1):67-70. Ann Genet. 1975. PMID: 1080040 French.
-
Trisomy of the short arm of chromosome 4: the changing phenotype with age.Ann Genet. 1992;35(4):217-23. Ann Genet. 1992. PMID: 1296518 Review.
-
[Trisomy 22. A new case].Ann Pediatr (Paris). 1976 Nov 2;23(11):705-11. Ann Pediatr (Paris). 1976. PMID: 16106879 Review. French. No abstract available.
Cited by
-
47,+(9q-) in unrelated three children with plasma growth hormone deficiency.Hum Genet. 1976 Mar 12;31(3):271-82. doi: 10.1007/BF00270857. Hum Genet. 1976. PMID: 955626
-
Partial 9 trisomy by 3:1 segregation of balanced maternal translocation (7q+; 9q-).J Med Genet. 1975 Sep;12(3):301-5. doi: 10.1136/jmg.12.3.301. J Med Genet. 1975. PMID: 1177284 Free PMC article.
-
A new case of trisomy for the short arm of No. 9 chromosome.J Med Genet. 1973 Sep;10(3):296-9. doi: 10.1136/jmg.10.3.296. J Med Genet. 1973. PMID: 4774540 Free PMC article.
-
Trisomy 12p due to familial t(12p-,6q plus) translocation.Humangenetik. 1974;24(3):247-52. Humangenetik. 1974. PMID: 4140836 No abstract available.
-
Trisomy 9p resulting from maternal 9/21 translocation.Hum Genet. 1976 May 19;32(2):217-20. doi: 10.1007/BF00291508. Hum Genet. 1976. PMID: 944684
MeSH terms
LinkOut - more resources
Miscellaneous