doi: 10.1111/j.1399-0004.1980.tb01789.x.
Prenatal diagnosis of a de novo reciprocal translocation 46,XX,t(1;18) (p22;q23)
- PMID: 7449182
- DOI: 10.1111/j.1399-0004.1980.tb01789.x
Item in Clipboard
Prenatal diagnosis of a de novo reciprocal translocation 46,XX,t(1;18) (p22;q23)
Clin Genet.
1980 Dec.
No abstract available
Similar articles
-
A de novo translocation in a family with a balanced reciprocal chromosomal translocation.Clin Genet. 1986 Feb;29(2):143-6. doi: 10.1111/j.1399-0004.1986.tb01238.x. Clin Genet. 1986. PMID: 3955864
-
[Double translocation 46, XX, t(2; 5), t(2; 18) with major reproduction problems].J Genet Hum. 1988 Jan;36(1-2):89-92. J Genet Hum. 1988. PMID: 3379383 French.
-
[Prenatal diagnosis of the cri-du-chat syndrome in the case of balanced 5p--; 18p+ translocation in the mother].Genetika. 1981;17(7):1304-8. Genetika. 1981. PMID: 7196856 Russian.
-
Prenatal diagnosis of a fetus with two balanced de novo chromosome rearrangements.Am J Med Genet. 1996 Dec 11;66(2):197-9. doi: 10.1002/(SICI)1096-8628(19961211)66:2<197::AID-AJMG14>3.0.CO;2-O. Am J Med Genet. 1996. PMID: 8958330 Review.
-
Mesomelic form of chondrodysplasia and congenital glaucoma associated with de novo translocation (13;18)(q14;q23).Genet Couns. 2004;15(2):191-7. Genet Couns. 2004. PMID: 15287419 Review.
Cited by
-
Reciprocal translocation t(1;18)(p32;q21) in a patient with some phenotypical anomalies.Hum Genet. 1987 Dec;77(4):384. doi: 10.1007/BF00291431. Hum Genet. 1987. PMID: 3692481 No abstract available.
-
Acrocephalopolysyndactyly, pentalogy of Fallot, and hypoacusis in a patient with a de novo reciprocal translocation involving the short arm of chromosome 1 and the long arm of chromosome 18: 46,XX,t(1;18)(p31;q11).J Med Genet. 1993 May;30(5):438-9. doi: 10.1136/jmg.30.5.438. J Med Genet. 1993. PMID: 8320714 Free PMC article.
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
