Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 [2 cases of trisomy 11q(q231--qter) by translocation t(11;22) (q231;q111) in 2 different families].

Literature DB >> 1080981

[2 cases of trisomy 11q(q231--qter) by translocation t(11;22) (q231;q111) in 2 different families].

A Aurias, C Turc, Y Michiels, P M Sinet, D Graveleau, J Lejeune.

Abstract

Two cases of partial trisomy 11q are reported, both apparently due to segregation in both patients' families of the same translocation between a n degrees 11 and a n degrees 22. R-, T-, and G- banding showed the breakage points to be 11q231 and 22q111. The clinical syndrome results from trisomy for the q231 leads to qter segment of chromosome 11.

Entities: Species

Mesh：

Year: 1975 PMID： 1080981

Source DB: PubMed Journal: Ann Genet ISSN： 0003-3995

Keyword Cloud
Cited

15 in total

1. At least nine cases of trisomy 11q23-->qter in one generation as a result of familial t(11;13) translocation.

Authors: D Smeets; C van Ravenswaaij; J de Pater; K Gerssen-Schoorl; J Van Hemel; G Janssen; A Smits
Journal: J Med Genet Date: 1997-01 Impact factor: 6.318

2. 47,XY,+der(11;22)(q23;q12) following balanced translocation t(11;22)(q23;q12)mat. Remarks on the problem of trisomy 22.

Authors: E Kessel; R A Pfeiffer
Journal: Hum Genet Date: 1977-06-10 Impact factor: 4.132

3. Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis.

Authors: D H Lockwood; A Farrier; F Hecht; J Allanson
Journal: Hum Genet Date: 1989-10 Impact factor: 4.132

Review 4. Factors predisposing to adjacent 2 and 3:1 disjunctions: study of 161 human reciprocal translocations.

Authors: P Jalbert; B Sele
Journal: J Med Genet Date: 1979-12 Impact factor: 6.318

5. 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

6. Incomplete trisomy 22. I. Familial 11/22 translocation with 3:1 meiotic disjunction. Delineation of a common clinical picture and report of nine new cases from six families.

Authors: A Schinzel; W Schmid; P Auf der Maur; H Moser; K H Degenhardt; M Geisler; A Grubisic
Journal: Hum Genet Date: 1981 Impact factor: 4.132

[2 cases of trisomy 11q(q231--qter) by translocation t(11;22) (q231;q111) in 2 different families].

1. At least nine cases of trisomy 11q23-->qter in one generation as a result of familial t(11;13) translocation.

2. 47,XY,+der(11;22)(q23;q12) following balanced translocation t(11;22)(q23;q12)mat. Remarks on the problem of trisomy 22.

3. Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis.

Review 4. Factors predisposing to adjacent 2 and 3:1 disjunctions: study of 161 human reciprocal translocations.

5. The problem of partial trisomy 22 reconsidered.

6. Incomplete trisomy 22. I. Familial 11/22 translocation with 3:1 meiotic disjunction. Delineation of a common clinical picture and report of nine new cases from six families.

7. Reciprocal translocations: a way to predict the mode of imbalanced segregation by pachytene-diagram drawing.

8. The aetiology of the cat eye syndrome reconsidered.

9. Assignment of human uroporphyrinogen I synthase locus to region 11qter by gene dosage effect.

10. Systematic analysis of 95 reciprocal translocations of autosomes.