Literature DB >> 8244343

A rare reciprocal translocation (12;21) segregating for nine generations.

S Koskinen1, T Onnelainen, A de la Chapelle, J Kere.   

Abstract

An autosomal reciprocal translocation (12;21) was found in five seemingly unrelated families in Finland. Three families had had multiple spontaneous abortions and two families had a child with Down's syndrome. The genealogies of the five families were traced using population registries, and four families were found to have a common ancestor born in 1752. Kinship to the fifth family could not be established but its ancestors were traced back to the same rural parishes as those of the four other families. The translocation segregated at the same frequency as normal chromosomes. A statistically insignificant increase in spontaneous abortions was detected when the matings of translocation carriers were compared with non-carrier matings. The increase may however be clinically significant. These results permit more accurate counselling in these and similar translocation families.

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Year:  1993        PMID: 8244343     DOI: 10.1007/bf00216460

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  20 in total

1.  Refined sublocalization of the human gene encoding the beta subunit of the S100 protein (S100B) and confirmation of a subtle t(9;21) translocation using in situ hybridization.

Authors:  A M Duncan; J Higgins; R J Dunn; R Allore; A Marks
Journal:  Cytogenet Cell Genet       Date:  1989

2.  First-trimester prenatal diagnosis of homozygous (14;21) translocation in a fetus with 44 chromosomes.

Authors:  B Dallapiccola; G Ferranti; D Altissimi; F Colloridi; R Paesano
Journal:  Prenat Diagn       Date:  1989-08       Impact factor: 3.050

3.  Partial trisomy 12 in a mentally retarded boy and translocation (12;21) in his mother.

Authors:  N Hobolth; P Jacobsen; M Mikkelsen
Journal:  J Med Genet       Date:  1974-09       Impact factor: 6.318

4.  Rare translocation 47,XY,t(12;21) in Down's syndrome.

Authors:  M Mikkelsen
Journal:  Hum Hered       Date:  1974       Impact factor: 0.444

5.  Partial trisomy 16q in the son resulting from paternal 16/21 translocation.

Authors:  M Kosanović; L Lopicić; V Diklić; J Nikolis
Journal:  Acta Med Iugosl       Date:  1983

6.  [Maternal t(7 ;21) translocation. Balanced karyotype in the fetus].

Authors:  P Colombies; G Bourrouillou; M P Ponsy; C Pellegry-Mounie
Journal:  Presse Med       Date:  1983-12-24       Impact factor: 1.228

7.  Translocations involving chromosome 12. I. A report of a 12,21 translocation in a woman with recurrent abortions, and a study of the breakpoints and modes of ascertainment of translocations involving chromosome 12.

Authors:  J H Ford; R H Rofe; R P Pavy
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

8.  Molecular study of parental origin of extra chromosome 21 in regular and de novo translocation trisomies.

Authors:  C Brahe; F Tassone; A Moscetti; A Millington-Ward; R Bova; A Serra
Journal:  Am J Med Genet Suppl       Date:  1990

9.  Meiotic and synaptonemal complex studies in a 14/21 translocation carrier.

Authors:  F Vidal; C Templado; J Navarro; S Marina; J Egozcue
Journal:  Int J Androl       Date:  1982-02

10.  Trisomy 12p syndrome. Evaluation of a family with a t(12;21) (p12.1;p11) translocation with unbalanced offspring.

Authors:  I L Hansteen; L Schirmer; S Hestetun
Journal:  Clin Genet       Date:  1978-04       Impact factor: 4.438

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