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Literature DB >> 123589

Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring.

Abstract

Five cases of chromosome imbalance resulting from 3:1 disjunction of reciprocal translocations are described. A review of the literature suggests this phenomenon is more common than has previously been recognized.

Entities: Species

Mesh：

Year: 1975 PMID： 123589 PMCID： PMC1013228 DOI： 10.1136/jmg.12.1.29

Source DB: PubMed Journal: J Med Genet ISSN： 0022-2593 Impact factor: 6.318

99 in total

1. Tandem translocation 15-13.

Authors: F Pasquali; O Zuffardi; F Severi; A Colombo; G R Burgio
Journal: Ann Genet Date: 1973-03

2. Precise identification of various chromosomal abnormalities.

Authors: K Hirschhorn; M Lucas; I Wallace
Journal: Ann Hum Genet Date: 1973-04 Impact factor: 1.670

3. [t(7q-; 21q-plus) and familial and trisomy 21].

Authors: F Giraud; M Hartung; J F Mattei; M G Mattie
Journal: Ann Genet Date: 1974-03

4. A cytogenetic survey of 11,680 newborn infants.

Authors: P A Jacobs; M Melville; S Ratcliffe; A J Keay; J Syme
Journal: Ann Hum Genet Date: 1974-05 Impact factor: 1.670

5. Down's syndrome. The possibility of a pathogenetic segment on chromosome no. 21.

Authors: E Niebuhr
Journal: Humangenetik Date: 1974-01-22

6. Sporadic (GqGq) translocations in Down's syndrome.

Authors: K L Ying
Journal: Can J Genet Cytol Date: 1973-06

7. Structural abnormalities of chromosome 18. 3. Two G-18 translocations, one identified AS 22-18.

Authors: M Fraccaro; P Herin; M Hultén; B I Ivemark; J Jonasson; J Lindsten; L Tiepolo; P Zetterqvist
Journal: Ann Genet Date: 1972-06

8. [Deletion of the short arm of chromosome 18 due to t(22-;18p+) translocation with IgA deficiency. Cytogenetic study with autoradiography and fluorescence].

Authors: S Gilgenkrantz; J M Charles; C Cabrol; G Mauuary; C Vigneron
Journal: Ann Genet Date: 1972-12

9. An 18p21q translocation in a patient with presumptive "monosomy G".

Authors: M M Cohen; T I Putnam
Journal: Am J Dis Child Date: 1972-12

10. High resolution studies on the pattern of induced exchanges in the human karyotype.

Authors: M Seabright
Journal: Chromosoma Date: 1973 Impact factor: 4.316

45 in total

1. Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) families.

Authors: T H Shaikh; M L Budarf; L Celle; E H Zackai; B S Emanuel
Journal: Am J Hum Genet Date: 1999-12 Impact factor: 11.025

2. Trisomy 9p and unusual translocation mongolism in siblings due to different 3:1 segregations of maternal translocation rcp(9;21)(p11;q11).

Authors: M Habedank; J Faust
Journal: Hum Genet Date: 1978-06-27 Impact factor: 4.132

3. The occurrence of a ring 18, an accessory bisatellited fragment, and trisomy 21 within one sibship.

Authors: E Grace; J Sills
Journal: Hum Genet Date: 1978-07-12 Impact factor: 4.132

4. Familial translocation t(lp--;21q+) associated with Down's syndrome.

Authors: E Kubień; A Kleczkowska
Journal: Hum Genet Date: 1978-02-16 Impact factor: 4.132

5. A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21).

Authors: Molly B Sheridan; Takema Kato; Chad Haldeman-Englert; G Reza Jalali; Jeff M Milunsky; Ying Zou; Ruediger Klaes; Georgio Gimelli; Stefania Gimelli; Robert M Gemmill; Harry A Drabkin; April M Hacker; Julia Brown; David Tomkins; Tamim H Shaikh; Hiroki Kurahashi; Elaine H Zackai; Beverly S Emanuel
Journal: Am J Hum Genet Date: 2010-07-30 Impact factor: 11.025