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Literature DB >> 4225661

Atypical acrocentric chromosomes in Negro and Caucasian Mongols.

M N Starkman, M W Shaw.

Abstract

Mesh：

Year: 1967 PMID： 4225661 PMCID： PMC1706145

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

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19 in total

1. AN EXTRA ABNORMAL CHROMOSOME IN A CHILD WITH MONGOLISM AND ACUTE MYELOBLASTIC LEUKEMIA. REPORT OF A CASE.

Authors: R D MERCER; M K KELLER; D LONSDALE
Journal: Cleve Clin Q Date: 1963-10

2. QUANTITATIVE STUDIES ON A2, SICKLE CELL, AND FETAL HEMOGLOBINS IN NEGROES WITH MONGOLISM, WITH OBSERVATIONS ON TRANSLOCATION MONGOLISM IN NEGROES.

Authors: E D WEINSTEIN; D L RUCKNAGEL; M W SHAW
Journal: Am J Hum Genet Date: 1965-09 Impact factor: 11.025

3. A chromosome abnormality with fragment in a paramongol child.

Authors: B R MIGEON; B N KAUFMANN; W J YOUNG
Journal: Bull Johns Hopkins Hosp Date: 1962-10

4. Enlarged satellites as a familial chromosome marker.

Authors: H L COOPER; K HIRSCHHORN
Journal: Am J Hum Genet Date: 1962-06 Impact factor: 11.025

5. Nucleolus-organisers in the causation of chromosomal anomalies in man.

Authors: S OHNO; J M TRUJILLO; W D KAPLAN; R KINOSITA
Journal: Lancet Date: 1961-07-15 Impact factor: 79.321

6. 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

7. Human oogenesis.

Authors: S OHNO; H P KLINGER; N B ATKIN
Journal: Cytogenetics Date: 1962

8. Racial differences in the length of the human Y chromosome.

Authors: M M Cohen; M W Shaw; J W MacCluer
Journal: Cytogenetics Date: 1966

9. Autosomal polymorphism via a translocation in the guinea pig, Cavia porcellus L.

Authors: M M Cohen; L Pinsky
Journal: Cytogenetics Date: 1966

10. Chromosome studies on randomly chosen men and women.

Authors: W M Brown; P A Jacobs; M Brunton
Journal: Lancet Date: 1965-09-18 Impact factor: 79.321

15 in total

1. Human karyotype polymorphism. III. Routine ank fluorescence microscopic investigation of chromosomes in normal adults and mentally retarded children.

Authors: A V Mikelsaar; M E Käosaar; S J Tüür; M H Viikmaa; T A Talvik; J Lääts
Journal: Humangenetik Date: 1975

2. Down's syndrome and deletion of short arms of a G chromosome.

Authors: G H Ballantyne; M I Parslow; A M Veale; D H Pullon
Journal: J Med Genet Date: 1977-04 Impact factor: 6.318

3. Familial 13p+ chromosome with mental retardation and dysmorphic features of two children.

Authors: C Stoll; A Rohmer; R Korn; G Heumann
Journal: Hum Genet Date: 1976-09-10 Impact factor: 4.132

4. Familial short arm deletion of chromosome no. 15.

Authors: J J Hoo; U Hillig; H Cramer; S Hansen; F Hermann
Journal: Humangenetik Date: 1974

5. Frequency of deletion of short arm satellites in acrocentric chromosomes.

Authors: J Nielsen; U Friedrich; A B Hreidarsson
Journal: J Med Genet Date: 1974-06 Impact factor: 6.318

Review 6. Satellite DNA.

Authors: K W Jones
Journal: J Med Genet Date: 1973-09 Impact factor: 6.318

10. [To the genetics and clinical aspects of small chromosome aberrations. A chromosome Gp-h and a chromosome Gs- in one family].

Authors: U Wolf; H Reinwein; H Lohmann
Journal: Humangenetik Date: 1968