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Literature DB >> 1248831

Partial trisomy 11,46,XX,-3,-20, + der3, + der20,t(3:11:20), resulting from a complex maternal rearrangement of chromosomes 3, 11, 20.

C G Palmer, C Poland, T Reed, J Kojetin.

Abstract

Clinical findings of partial trisomy 11p are described in a patient bearing t(3;11;20) (p13;p11;q13). The translocation was present in balanced form in her mother (46, XX)t(3;11;20) (p13;p11;q13).

Entities: Gene Species

Mesh：

Year: 1976 PMID： 1248831 DOI： 10.1007/bf00296149

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

14 in total

1. Familial balanced (7;11;21) translocation and Down's syndrome in two siblings.

Authors: E Schwinger; M Mikkelsen; M Niesen
Journal: Clin Genet Date: 1975-04 Impact factor: 4.438

2. [Crying cat disease associated with complex chromosome rearrangement in a dizygotic twin].

Authors: J L Taillemite; G Baheux-Morlier; L Cathelineau; C Roux
Journal: Ann Genet Date: 1973-06

3. [Complexe de novo rearrangement involving 4 chromosomes in a newborn infant].

Authors: J Martinetti; B Noel
Journal: Ann Genet Date: 1973-12

4. Complex five-break rearrangement.

Authors: M G Fitzgerald
Journal: Clin Genet Date: 1974-01 Impact factor: 4.438

5. Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13.

Authors: O Sanchez; J J Yunis; J I Escobar
Journal: Humangenetik Date: 1974-04-24

6. Partial trisomy of chromosome 11: a case report.

Authors: R E Falk; R E Carrel; M Valente; B F Crandall; R S Sparkes
Journal: Am J Ment Defic Date: 1973-01

7. A pericentric inversion, 5 p-q+, and additional complex rearrangements in a case of cri-du-chat syndrome.

Authors: A Catti; W Schmid
Journal: Cytogenetics Date: 1971

8. A case of multople chromosomal rearrangements with persistence of foetal haemoglobin.

Authors: F Nuzzo; A Marini; C Baglioni; C E Ford; L De Carli; L Piceni Sereni
Journal: Cytogenetics Date: 1968

9. A complex familial translocation involving chromosomes 5, 9 and 13.

Authors: K Fredga; B Hall
Journal: Cytogenetics Date: 1970

10. Possible complex translocation t(9;14;13) (q12;pl?;Q31) in mother of a child with 9-p trisomy syndrome.

Authors: H Fujita; T Abe; K Yamamoto; J Furuyama
Journal: Humangenetik Date: 1974

8 in total

1. Prenatal diagnosis and follow up of a child with a complex chromosome rearrangement.

Authors: M H Bogart; C L Bradshaw; O W Jones; J E Schanberger
Journal: J Med Genet Date: 1986-04 Impact factor: 6.318

2. Familial complex autosomal translocations involving chromosomes 7, 8, and 9 exhibiting male and female transmission with segregation and recombination.

Authors: S Walker; P J Howard; D Hunter
Journal: J Med Genet Date: 1985-12 Impact factor: 6.318

8. A woman carrier of two apparently unrelated reciprocal translocations: prenatal diagnosis of normal karyotype in the foetus.

Authors: G Simoni; E Montali; F Rossella; L Dalprà; F Lo Curto
Journal: Hum Genet Date: 1979-01-25 Impact factor: 4.132