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Literature DB >> 5097902

Patterns of D chromosome involvement in human (DqDq) and (DqGq) Robertsonian rearrangements.

F Hecht, W J Kimberling.

Abstract

Entities: Species

Mesh：

Substances：
Tritium
Thymidine

Year: 1971 PMID： 5097902 PMCID： PMC1706712

Source DB: PubMed Journal: Am J Hum Genet ISSN： 0002-9297 Impact factor: 11.025

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33 in total

1. Nonrandomness of translocations in man: preferential entry of chromosomes into 13-15-21 translocations.

Authors: F Hecht; M P Case; E W Lovrien; J V Higgins; H C Thuline; J Melnyk
Journal: Science Date: 1968-07-26 Impact factor: 47.728

2. D/D balanced translocations.

Authors: J Ott; A Robinson; D C Peakman
Journal: Lancet Date: 1968-12-21 Impact factor: 79.321

3. Trisomy D1 with two D-D translocation chromosomes. Report of a case.

Authors: M M Cohen; N Takagi; E K Harrod
Journal: Am J Dis Child Date: 1968-02

4. A family with D-D translocation.

Authors: E Krmpotic; K Ramanathan; A Grossman
Journal: J Med Genet Date: 1968-09 Impact factor: 6.318

5. A chromosome survey of 2,400 normal newborn infants.

Authors: S Walzer; G Breau; P S Gerald
Journal: J Pediatr Date: 1969-03 Impact factor: 4.406

6. A mouse translocation with 38 and 39 chromosomes but normal N. F.

Authors: B J White; J H Tjio
Journal: Hereditas Date: 1967 Impact factor: 3.271

7. Transmission of a D/D reciprocal translocation in a family with high incidence of mental retardation.

Authors: A S Dekaban
Journal: Am J Hum Genet Date: 1966-05 Impact factor: 11.025

8. A new marker for chromosome studies in the mouse.

Authors: A Léonard; G Deknudt
Journal: Nature Date: 1967-04-29 Impact factor: 49.962

9. The identification of the chromosomes of the D group (13-15) Denver: an autoradiographic and measurement study.

Authors: F Giannelli; R M Howlett
Journal: Cytogenetics Date: 1966

10. Identification of translocated chromosomes by means of autoradiography.

Authors: M Higurashi; Y Nakagome; T Nagao; M Naganuma; I Matsui
Journal: Paediatr Univ Tokyo Date: 1967-06

18 in total

1. Identification and characterization of satellite III subfamilies to the acrocentric chromosomes.

Authors: R Bandyopadhyay; C McQuillan; S L Page; K H Choo; L G Shaffer
Journal: Chromosome Res Date: 2001 Impact factor: 5.239

2. Transmission of a t(13q22q) chromosome observed in three generations with segregation of the translocation D1-trisomy syndrome.

Authors: T Abe; M Morita; K Kawai; S Misawa; H Kanai; G Hirose; H Fujita
Journal: Humangenetik Date: 1975-09-20

3. The Prader-Willi syndrome with a 15/15 translocation. Case report and review of the literature.

Authors: C J Hawkey; A Smithies
Journal: J Med Genet Date: 1976-04 Impact factor: 6.318

4. De novo 21/21 translocation Down syndrome. Studies of parental origin of the translocation and acrocentric associations in parents.

Authors: J Nikolis; V Kekić
Journal: Hum Genet Date: 1986-06 Impact factor: 4.132

9. Structural basis for Robertsonian translocations in man: association of ribosomal genes in the nucleolar fibrillar center in meiotic spermatocytes and oocytes.

Authors: A Stahl; J M Luciani; M Hartung; M Devictor; J L Bergé-Lefranc; M Guichaoua
Journal: Proc Natl Acad Sci U S A Date: 1983-10 Impact factor: 11.205

10. A girl with the Prader-Willi syndrome and Robertsonian translocation 45,XX,t(14;15)(p11;q11) which was present in three normal family members.

Authors: A Smith; M Noel
Journal: Hum Genet Date: 1980 Impact factor: 4.132