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A familial variant of chromosome 9.

Data up to Jan 2025

Published1971
Citations28
References22

Total Citations Per Year

Abstract

References (22)

Sequential tests for the detection of linkage.

1955 • 1,590 citations

Meiotic Drive as an Evolutionary Force

1957 • 455 citations

Probable assignment of the Duffy blood group locus to chromosome 1 in man.

1968 • 276 citations

EFFECTS OF MITOMYCIN C ON HUMAN CHROMOSOMES

1964 • 171 citations

Enhancement of Secondary Constrictions and the Heterochromatic X in Human Cells

1962 • 125 citations

THE EFFECT OF ABNORMAL CHROMOSOME 10 ON PREFERENTIAL SEGREGATION AND CROSSING OVER IN MAIZE

1966 • 124 citations

Chromosome studies on adults

1966 • 123 citations

Chromosome Studies on Adults

1967 • 101 citations

Secondary Constrictions in Human Chromosomes

1965 • 56 citations

Chromosomal study in patients with cysts of the jaw, multiple nevoid basal cell carcinomata and bifid rib syndrome

1963 • 53 citations

The effect of 5-bromodeoxyuridine on human chromosomes

1964 • 50 citations

ASYMMETRY OF CHROMOSOME NUMBER 1 PAIR IN THREE GENERATIONS OF A PHENOTYPICALLY NORMAL FAMILY

1968 • 41 citations

A FAMILIAL CHROMOSOME VARIANT IN A SUBJECT WITH ANOMALOUS SEX DIFFERENTIATION.

1963 • 37 citations

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

1969 • 33 citations

Inheritance of marker chromosomes from a cytogenetic survey of congenital heart disease

1966 • 31 citations

A GENETIC STUDY OF SEGREGATION IN A TRANSLOCATION HETEROZYGOTE IN DROSOPHILA

1955 • 22 citations

THE IDIOGRAM OF THE SHEEP WITH PARTICULAR REFERENCE TO SECONDARY CONSTRICTIONS

1967 • 19 citations

Preferential Segregation of Chromosomes from a Trivalent in Haplopappus gracilis

1964 • 19 citations

Short arm enlargement in acrocentric chromosomes.

1969 • 17 citations

Genetic linkage analysis of human hemoglobin variants.

1970 • 13 citations

Anomalie d'un chromosome du groupe C chez plusieurs membres d'une m�me famille

1968 • 3 citations

A CASE OF WERDNIG-HOFFMAN MUSCULAR DYSTROPHY WITH AN UNUSUAL CHROMOSOME COMPLEMENT

2009 • 3 citations

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A familial variant of chromosome 9. (1971) – Journal of Medical Genetics | Metascience Observatory Explorer