Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21).

A RAPID BANDING TECHNIQUE FOR HUMAN CHROMOSOMES

1971 • 5,049 citations

Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome.

1968 • 347 citations

Congenital Malformations in Autosomal Trisomy Syndromes

1966 • 237 citations

The 13q-deletion syndrome.

1969 • 152 citations

Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations.

1972 • 116 citations

The cri du chat syndrome in adolescents and adults: Clinical finding in 13 older patients with partial deletion of the short arm of chromosome No. 5(5p-)

1970 • 86 citations

New Syndrome of Neonatal Hypoglycemia

1966 • 70 citations

An investigation of 69 cases of exomphalos.

1953 • 59 citations

Partial deletion of the short arm of chromosome No. 4(4p-): Clinical studies in five unrelated patients

1970 • 54 citations

Chromosome analysis of two related heteroploid mouse cell lines by quinacrine fluorescence

1973 • 46 citations

GENETIC ASPECTS OF ABORTION

1959 • 38 citations

Familial Chromosome-2, 3 Translocation Ascertained through an Infant with Multiple Malformations

1964 • 29 citations

Assignment of the Human Gene for Hexose-1-phosphate Uridylyltransferase to Chromosome 3

1974 • 24 citations

Familial 2/3 translocation.

1966 • 18 citations

Familial 2/3 translocation.

1967 • 13 citations

LOCALISATION OF HUMAN GENE FOR GALACTOSE-1-PHOSPHATE-URIDYLTRANS-FERASE

1975 • 10 citations