Literature DB >> 5563410

Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocation.

H Hoehn, W Engel, H Reinwein.   

Abstract

Mesh：

Year:  1971        PMID： 5563410     DOI： 10.1007/bf00702772

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


× No keyword cloud information.
  7 in total

1.  Spontaneous fragility of an abnormally wide secondary constriction region in a human chromosome no. 9.

Authors:  W Schmid; D Vischer
Journal:  Humangenetik       Date:  1969

2.  Satellite DNA associated with heterochromatin in Rhynchosciara.

Authors:  R A Eckhardt; J G Gall
Journal:  Chromosoma       Date:  1971-03-16       Impact factor: 4.316

3.  Preferential breakage of sensitive regions of human chromosomes.

Authors:  B R Reeves; S D Lawler
Journal:  Humangenetik       Date:  1970

4.  [4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity].

Authors:  M O Rethoré; L Larget-Piet; D Abonyi; M Boeswillwald; R Berger; S Carpentier; J Cruveiller; B Dutrillau; J Lafourcade; M Penneau; J Lejeune
Journal:  Ann Genet       Date:  1970-12

5.  Familial transmission of an unusual variant of a group C chromosome.

Authors:  E Tuckerman; J E Gray; J Salmon
Journal:  Ann Genet       Date:  1970-09

6.  [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

7.  Deletions of the X chromosomes in Microtus agrestis cells in vitro.

Authors:  J E Cooper; F E Arrighi; T C Hsu
Journal:  Cytogenetics       Date:  1970
  7 in total
  17 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

2.  A case of partial (9p) trisomy in a family with a balanced translocation 46,XX,t(1p+9q-).

Authors:  M K Mason; D A Spencer; A Rutter
Journal:  J Med Genet       Date:  1975-09       Impact factor: 6.318

3.  Possible intrachromosomal duplication in a case of trisomy 9p.

Authors:  H Chiyo; J Furuyama; N Suehara; Y Obashi; H Kikkawa
Journal:  Hum Genet       Date:  1976-10-28       Impact factor: 4.132

4.  A case of trisomy for the short arm of chromosome no. 9(+9(p)).

Authors:  M E Käosaar; A V Mikelsaar; T A Talvik; R V Mikelsaar
Journal:  Hum Genet       Date:  1976-09-10       Impact factor: 4.132

5.  Trisomy 9p resulting from maternal 9/21 translocation.

Authors:  I Sŭbrt; B Blehová; B Pallová
Journal:  Hum Genet       Date:  1976-05-19       Impact factor: 4.132

6.  47,+(9q-) in unrelated three children with plasma growth hormone deficiency.

Authors:  H Fujita; M Shimazaki; T Takeuchi; Y Hayakawa; T Oura
Journal:  Hum Genet       Date:  1976-03-12       Impact factor: 4.132

7.  De novo trisomy 9pter leads to q13.

Authors:  N B Kardon; H R Salwen; M A Krauss; J G Davis; E C Jenkins
Journal:  Hum Genet       Date:  1977-06-30       Impact factor: 4.132

8.  Partial trisomy 9 with resemblance to Coffin-Siris syndrome.

Authors:  T Kushnick; G M Adessa
Journal:  J Med Genet       Date:  1976-06       Impact factor: 6.318

Review 9.  Genetics of the +p9 syndrome.

Authors:  I W Lurie; G I Lazjuk; D B Gurevich; S S Usoev
Journal:  Hum Genet       Date:  1976-04-15       Impact factor: 4.132

10.  Partial 9 trisomy by 3:1 segregation of balanced maternal translocation (7q+; 9q-).

Authors:  V B Penehaszadeh; R Coco
Journal:  J Med Genet       Date:  1975-09       Impact factor: 6.318
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.