Literature DB >> 7203479

The 11q;22q translocation: a European collaborative analysis of 43 cases.

M Fraccaro, J Lindsten, C E Ford, L Iselius.   

Abstract

Mesh：

Year:  1980        PMID： 7203479     DOI： 10.1007/bf00281567

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


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  22 in total

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

Authors:  R H Lindenbaum; M Bobrow
Journal:  J Med Genet       Date:  1975-03       Impact factor: 6.318

2.  Abnormal chromosome 22 and recurrence of trisomy-22 syndrome.

Authors:  B S Emanuel; E H Zackai; M M Aronson; W J Mellman; P S Moorhead
Journal:  J Med Genet       Date:  1976-12       Impact factor: 6.318

3.  Balanced translocation, impaired sperm motility, and offspring anomaly.

Authors:  J R Oakley; P Else; P Asplin; L S Taitz
Journal:  Arch Dis Child       Date:  1976-08       Impact factor: 3.791

4.  Cat eye syndrome. Partial trisomy 22 due to translocation in the mother.

Authors:  M K Bofinger; S W Soukup
Journal:  Am J Dis Child       Date:  1977-08

5.  Transposition of 9q34 and 22 (q11toqter) regions has a specific role in chronic myelocytic leukemia.

Authors:  F Pasquali; R Casalone; D Francesconi; D Peretti; M Fraccaro; C Bernasconi; M Lazzarino
Journal:  Hum Genet       Date:  1979-11-01       Impact factor: 4.132

6.  A deleted extra chromosome 22 identified by DNA replication banding.

Authors:  M Parslow; J J Hoo; M Garry; F Rose
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

7.  The problem of partial trisomy 22 reconsidered.

Authors:  G M Feldman; R S Sparkes
Journal:  Hum Genet       Date:  1978-11-24       Impact factor: 4.132

8.  Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction.

Authors:  E H Zackai; B S Emanuel
Journal:  Am J Med Genet       Date:  1980

9.  A case of chronic myelogenous leukemia (CML) with a translocation between chromosomes 12 and 22, t(12;22)(p13;q13), resulting in a Philadelphia (Ph1) chromosome.

Authors:  R S Verma; H Dosik
Journal:  Cytogenet Cell Genet       Date:  1979

10.  [Trisomy 11q. Individualization of a new syndrome].

Authors:  A Aurias; C Laurent
Journal:  Ann Genet       Date:  1975-09
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  56 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.  Tightly clustered 11q23 and 22q11 breakpoints permit PCR-based detection of the recurrent constitutional t(11;22).

Authors:  H Kurahashi; T H Shaikh; E H Zackai; L Celle; D A Driscoll; M L Budarf; B S Emanuel
Journal:  Am J Hum Genet       Date:  2000-07-20       Impact factor: 11.025

3.  Meiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 MI segregation as the cause of liveborn offspring with an unbalanced translocation.

Authors:  S J Armstrong; A S Goldman; R M Speed; M A Hultén
Journal:  Am J Hum Genet       Date:  2000-08-08       Impact factor: 11.025

4.  AT-rich palindromes mediate the constitutional t(11;22) translocation.

Authors:  L Edelmann; E Spiteri; K Koren; V Pulijaal; M G Bialer; A Shanske; R Goldberg; B E Morrow
Journal:  Am J Hum Genet       Date:  2000-11-28       Impact factor: 11.025

5.  Polymorphisms of the 22q11.2 breakpoint region influence the frequency of de novo constitutional t(11;22)s in sperm.

Authors:  Maoqing Tong; Takema Kato; Kouji Yamada; Hidehito Inagaki; Hiroshi Kogo; Tamae Ohye; Makiko Tsutsumi; Jieru Wang; Beverly S Emanuel; Hiroki Kurahashi
Journal:  Hum Mol Genet       Date:  2010-04-13       Impact factor: 6.150

Review 6.  The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements.

Authors:  H Kurahashi; H Inagaki; T Ohye; H Kogo; M Tsutsumi; T Kato; M Tong; B S Emanuel
Journal:  Clin Genet       Date:  2010-10       Impact factor: 4.438

7.  Paternal origin of the de novo constitutional t(11;22)(q23;q11).

Authors:  Tamae Ohye; Hidehito Inagaki; Hiroshi Kogo; Makiko Tsutsumi; Takema Kato; Maoqing Tong; Merryn V E Macville; Livija Medne; Elaine H Zackai; Beverly S Emanuel; Hiroki Kurahashi
Journal:  Eur J Hum Genet       Date:  2010-02-24       Impact factor: 4.246

8.  A unique case of der(11)t(11;22),-22 arising from 3:1 segregation of a maternal t(11;22) in a family with co-segregation of the translocation and breast cancer.

Authors:  Vaidehi Jobanputra; Wendy K Chung; April M Hacker; Beverly S Emanuel; Dorothy Warburton
Journal:  Prenat Diagn       Date:  2005-08       Impact factor: 3.050

9.  XX male with sex reversal and a de novo 11;22 translocation.

Authors:  Merryn V E Macville; Wim H Loneus; Dominique Marcus-Soekarman; Erik H L P G Huys; Eric F P M Schoenmakers; April Schrank-Hacker; Beverly S Emanuel; John J M Engelen
Journal:  Am J Med Genet A       Date:  2006-09-15       Impact factor: 2.802

10.  "Partial trisomy 22 and 11" due to a paternal 11;22 translocation associated with Hirschsprung disease.

Authors:  B Beedgen; W Nützenadel; U Querfeld; P Weiss-Wichert
Journal:  Eur J Pediatr       Date:  1986-08       Impact factor: 3.183
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