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11 in total

1. Chromosome preparations of leukocytes cultured from human peripheral blood.

Authors: P S MOORHEAD; P C NOWELL; W J MELLMAN; D M BATTIPS; D A HUNGERFORD
Journal: Exp Cell Res Date: 1960-09 Impact factor: 3.905

2. A Transmissible Dicentric Chromosome.

Authors: E R Sears; A Câmara
Journal: Genetics Date: 1952-03 Impact factor: 4.562

3. Down's syndrome associated with a familial (21q-; 22q+) translocation.

Authors: M M Cohen; R G Davidson
Journal: Cytogenetics Date: 1967

4. Identification of G-group chromosomes involved in a G-G tandem-translocation by the giemsa-band technique.

Authors: W Vogel
Journal: Humangenetik Date: 1972

5. Localization of heterochromatin in human chromosomes.

Authors: F E Arrighi; T C Hsu
Journal: Cytogenetics Date: 1971

6. Karyotype analysis utilizing differentially stained constitutive heterochromatin of human and murine chromosomes.

Authors: T R Chen; F H Ruddle
Journal: Chromosoma Date: 1971 Impact factor: 4.316

7. Fluorescent staining of human chromosomes: identification of some common aberrations.

Authors: I A Uchida; C C Lin
Journal: Can Med Assoc J Date: 1971-09-04 Impact factor: 8.262

8. Fluorescent chromosomes of a tandem translocation in a mongol patient.

Authors: S Sachdeva; J Wodnicki; G F Smith
Journal: J Ment Defic Res Date: 1971-09

9. [Tandem chromosome (G-G) with satellites on short and long arm in a patient with trisomy G1].

Authors: W Vogel; H Reinwein; W Engel
Journal: Humangenetik Date: 1970

10. [A case of G-G translocation in tandem].

Authors: J Lejeune; R Berger; O R Vidal; M O Réthoré
Journal: Ann Genet Date: 1965

7 in total

1. Down's syndrome. The possibility of a pathogenetic segment on chromosome no. 21.

Authors: E Niebuhr
Journal: Humangenetik Date: 1974-01-22

2. [Masculinization of XX males (author's transl)].

Authors: M Bartsch-Sandhoff; H Schade; W Wiegelmann; H G Solbach; W Scholz
Journal: Humangenetik Date: 1974

3. Mirror image duplications of chromosome 21. Three new cases and discussion of the mechanisms of origin.

Authors: R A Pfeiffer; J Loidl
Journal: Hum Genet Date: 1982 Impact factor: 4.132

4. Dicentric chromosome 13 and centromere inactivation.

Authors: S Schwartz; C G Palmer; D D Weaver; J Priest
Journal: Hum Genet Date: 1983 Impact factor: 4.132

5. Familial Down syndrome due to t(10;21) translocation: evidence that the Down phenotype is related to trisomy of a specific segment of chromosome 21.

Authors: J D Williams; R L Summitt; P R Martens; R A Kimbrell
Journal: Am J Hum Genet Date: 1975-07 Impact factor: 11.025

6. No significant effect of monosomy for distal 21q22.3 on the Down syndrome phenotype in "mirror" duplications of chromosome 21.

Authors: C Pangalos; D Théophile; P M Sinet; A Marks; D Stamboulieh-Abazis; Z Chettouh; M Prieur; C Verellen; M O Rethoré; J Lejeune
Journal: Am J Hum Genet Date: 1992-12 Impact factor: 11.025

7. Partial trisomy 21. Further evidence that trisomy of band 21q22 is essential for Down's phenotype.

Authors: A Hagemeijer; E M Smit
Journal: Hum Genet Date: 1977-08-31 Impact factor: 4.132

7 in total