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Literature DB >> 770307

Genetics of the +p9 syndrome.

I W Lurie, G I Lazjuk, D B Gurevich, S S Usoev.

Abstract

An analysis of data about the +p9 syndrome revealed that this clinical entity may occur in some different genetic forms. The recurrence risk in cases with familial translocations is due to the type of meiotic segregation, 2:2 or 3:1. It was shown a nonrandomness of involvement of chromosomes 15 and 22 in translocations with chromosome number 9.

Mesh：

Year: 1976 PMID： 770307 DOI： 10.1007/bf00569973

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

37 in total

1. Trisomy 9p in a girl whose mother has a translocation t(9;20)(q12;p13).

Authors: C Stoll; J M Levy; A Gardea
Journal: Humangenetik Date: 1975

Review 2. Partial monosomies 18. Review of cytogenetical and phenotypical variants.

Authors: I W Lurie; G I Lazjuk
Journal: Humangenetik Date: 1972

3. Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15pplus;9qminus) in three generations.

Authors: P E Podruch; B Weisskopf
Journal: J Pediatr Date: 1974-07 Impact factor: 4.406

4. [Partial tetrasomy of number 9 chromosome, and mosaicism in a child with multiple malformations (author's transl)].

Authors: D Ghymers; B Hermann; C Distèche; J Frederic
Journal: Humangenetik Date: 1973-12-10

5. 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

6. An inherited B-C translocation in a dysplastic girl with partial C trisomy.

Authors: B Hall; N Svenningsen
Journal: Acta Paediatr Scand Date: 1969-03

7. [Familial Cc-F translocation determining a trisomy for the short arm of chromosome 12].

Authors: J Lejeuen; R Berger; M O Réthoré; C Salmon; M Kaplan
Journal: Ann Genet Date: 1966

8. Additional small acrocentric chromosome: two cases.

Authors: J Nielsen; T Tsuboi; U Friedrich; M Mikkelsen; B Lund; O Steinicke
Journal: J Ment Defic Res Date: 1969-06

9. 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

10. Four cases of 9p trisomy resulting from a balanced familial translocation (9:15) (q13;q11). Clinical picture and cytogenetic findings.

Authors: J Zaremba; E Zdzienicka; I Glogowska; T Abramowicz; B Taracha
Journal: J Ment Defic Res Date: 1974-06

11 in total

1. 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

9. The quantitative analysis of polymorphism on human chromosomes 1, 9, 16, and Y. III. Study of relationships of C segments' lengths in individual karyotypes.

Authors: O A Podugolnikova
Journal: Hum Genet Date: 1979-07-18 Impact factor: 4.132

Review 10. Adjacent 2 meiotic disjunction. report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literature.

Authors: D P Duckett; S H Roberts
Journal: Hum Genet Date: 1981 Impact factor: 4.132

Genetics of the +p9 syndrome.

1. Trisomy 9p in a girl whose mother has a translocation t(9;20)(q12;p13).

Review 2. Partial monosomies 18. Review of cytogenetical and phenotypical variants.

3. Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15pplus;9qminus) in three generations.

4. [Partial tetrasomy of number 9 chromosome, and mosaicism in a child with multiple malformations (author's transl)].

5. Trisomy 22: a clinical entity.

6. An inherited B-C translocation in a dysplastic girl with partial C trisomy.

7. [Familial Cc-F translocation determining a trisomy for the short arm of chromosome 12].

8. Additional small acrocentric chromosome: two cases.

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

10. Four cases of 9p trisomy resulting from a balanced familial translocation (9:15) (q13;q11). Clinical picture and cytogenetic findings.

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

2. De novo trisomy 9pter leads to q13.

3. Familial trisomy 9p and spinal muscular atrophy: clinical, cytogenetic and embryological findings.

4. Duplication 9p due to unequal sister chromatid exchange.

5. t(9/22) with centric fission and NOR translocation leading to a case of pure 9p trisomy in the offspring.

6. Duplication of the short arm of chromosome 9. Analysis of five cases.

7. Trisomy 9p with i(9p) and t(9q18p).

8. Systematic analysis of 95 reciprocal translocations of autosomes.

9. The quantitative analysis of polymorphism on human chromosomes 1, 9, 16, and Y. III. Study of relationships of C segments' lengths in individual karyotypes.

Review 10. Adjacent 2 meiotic disjunction. report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literature.