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 Partial trisomy 8 (8q24) and the trisomy-8 syndrome.

Literature DB >> 4420964

Partial trisomy 8 (8q24) and the trisomy-8 syndrome.

O Sánchez, J J Yunis.

Abstract

Entities: Disease Gene

Mesh：

Year: 1974 PMID： 4420964 DOI： 10.1007/BF00272513

Source DB: PubMed Journal: Humangenetik ISSN： 0018-7348

× No keyword cloud information.

11 in total

1. Four patients with trisomy 8 identified by the fluorescence and Giemsa banding techniques.

Authors: T Caspersson; J Lindsten; L Zech; K E Buckton; W H Price
Journal: J Med Genet Date: 1972-03 Impact factor: 6.318

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. Probable trisomy 22 identified by fluorescent and trypsin-giemsa banding.

Authors: H N Bass; B F Crandall; R S Sparkes
Journal: Ann Genet Date: 1973-09

4. C8 trisomy mosaicism syndrome.

Authors: J B Bijlsma; J C Wijffels; W H Tegelaers
Journal: Helv Paediatr Acta Date: 1972-07

5. [Trisomy 8 with mosaicism].

Authors: G Malpuech; B Dutrillaux; Y Fonck; J Gaulme; B Bouche
Journal: Arch Fr Pediatr Date: 1972-10

6. Trisomy of the short arm of chromosome 8: association with translocation between chromosomes 8 and 22 46,XY,22-,t(8p22q) plus.

Authors: I M Rosenthal; E Krmpotic; M Bocian; K Szego
Journal: Clin Genet Date: 1973-06 Impact factor: 4.438

7. [Translocation 8-22 with no length change and partial trisomy for 8q. Detection by heat denaturation].

Authors: J Lejeune; M O Rethore; B Dutrillaux; G Martin
Journal: Exp Cell Res Date: 1972-09 Impact factor: 3.905

8. Trisomy 22: a clinical entity.

Authors: L Y Hsu; L R Shapiro; M Gertner; E Lieber; K Hirschhorn
Journal: J Pediatr Date: 1971-07 Impact factor: 4.406

9. [Clinical and cytogenetic observations on 2 mosaic C trisomic adults. Individualization of the supernumerary chromosome with the modern denaturation technic: 47, XY, ?8 +].

Authors: C Laurent; J M Robert; J Grambert; B Dutrillaux
Journal: Lyon Med Date: 1971-12-26

10. [Study by fluorescence of a trisomy C mosaic, probably 8: 46,XY-47,XY,?8+].

Authors: J de Grouchy; C Turleau; C Léonard
Journal: Ann Genet Date: 1971-03

13 in total

1. 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

2. Nonrandom distribution of exchange points in patients with structural rearrangements.

Authors: Y Nakagome; H Chiyo
Journal: Am J Hum Genet Date: 1976-01 Impact factor: 11.025

3. New chromosomal malformation syndromes. I. Partial monosomy 8p. An attempt to establish a new chromosome deletion syndrome.

Authors: A Rodewald; S Stengel-Rutkowski; P Schulz; H Cleve
Journal: Eur J Pediatr Date: 1977-04-26 Impact factor: 3.183

Partial trisomy 8 (8q24) and the trisomy-8 syndrome.

1. Four patients with trisomy 8 identified by the fluorescence and Giemsa banding techniques.

2. Precise identification of various chromosomal abnormalities.

3. Probable trisomy 22 identified by fluorescent and trypsin-giemsa banding.

4. C8 trisomy mosaicism syndrome.

5. [Trisomy 8 with mosaicism].

6. Trisomy of the short arm of chromosome 8: association with translocation between chromosomes 8 and 22 46,XY,22-,t(8p22q) plus.

7. [Translocation 8-22 with no length change and partial trisomy for 8q. Detection by heat denaturation].

8. Trisomy 22: a clinical entity.

9. [Clinical and cytogenetic observations on 2 mosaic C trisomic adults. Individualization of the supernumerary chromosome with the modern denaturation technic: 47, XY, ?8 +].

10. [Study by fluorescence of a trisomy C mosaic, probably 8: 46,XY-47,XY,?8+].

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

2. Nonrandom distribution of exchange points in patients with structural rearrangements.

3. New chromosomal malformation syndromes. I. Partial monosomy 8p. An attempt to establish a new chromosome deletion syndrome.

4. Partial trisomy 8q in half-sisters with distinct dysmorphic patterns not similar to the trisomy 8 mosaicism syndrome.

5. Partial trisomy 15q1.

6. Deletion of the long arm of chromosome 8 resulting from a de novo translocation t(4;8) (q13;q213).

7. Small structural changes of chromosome 8. Two cases with evidence for deletion.

8. A child with a recombinant of chromosome 8 inherited from her carrier mother.

9. Familial distal trisomy 8(q24.13----qter).

10. The G-banded prophase chromosomes of man.