Case Reports
[Mosaic trisomy 13 with isochromosome: 46, XX-46, XX, 13-, 13 q:]
[Article in
French]
- PMID: 4537722
Item in Clipboard
Case Reports
[Mosaic trisomy 13 with isochromosome: 46, XX-46, XX, 13-, 13 q:]
[Article in
French]
Ann Genet.
1972 Jun.
No abstract available
Similar articles
-
[Mosaic 14 trisomy in a female child with multiple abnormalities].Ann Genet. 1975 Mar;18(1):71-4. Ann Genet. 1975. PMID: 1080041 French.
-
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.
-
A mildly retarded woman with 46,XX/47,XX, + 18 mosaicism.Am J Med Genet. 1985 Oct;22(2):343-6. doi: 10.1002/ajmg.1320220218. Am J Med Genet. 1985. PMID: 4050867
-
Optic atrophy, microcephaly, mental retardation and mosaic variegated aneuploidy: a human mitotic mutation.Ann Genet. 1994;37(2):75-7. Ann Genet. 1994. PMID: 7985982 Review.
-
Mosaic isochromosome 8p.Am J Med Genet. 1993 Jun 15;46(5):517-9. doi: 10.1002/ajmg.1320460511. Am J Med Genet. 1993. PMID: 8322812 Review.
Cited by
-
A somatic origin of homologous Robertsonian translocations and isochromosomes.Am J Hum Genet. 1994 Feb;54(2):290-302. Am J Hum Genet. 1994. PMID: 8304346 Free PMC article.
-
Inheritance of a t(13;14)(q10;q10) Robertsonian translocation with a low level of trisomy 13 mosaicism.Eur J Pediatr. 2010 Jul;169(7):789-93. doi: 10.1007/s00431-009-1111-0. Epub 2009 Dec 3. Eur J Pediatr. 2010. PMID: 19957191
-
Trisomy 22 in a newborn with multiple malformations.Hum Genet. 1987 Jul;76(3):298-301. doi: 10.1007/BF00283629. Hum Genet. 1987. PMID: 3474207
-
Different forms of incomplete trisomy 13. Mosaicism and partial trisomy for the proxim.Humangenetik. 1974;22(4):287-98. doi: 10.1007/BF00295488. Humangenetik. 1974. PMID: 4139096 No abstract available.
-
Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX, - 13, + t(13;13)(p11;q11)/46,XX,del(13)(p11).Hum Genet. 1979 Jan 25;46(2):237-41. doi: 10.1007/BF00291927. Hum Genet. 1979. PMID: 422207