Mosaicism for deletion 1p36.33 in a patient with obesity and hyperphagia

Prader-Willi Syndrome: Consensus Diagnostic Criteria

1993 • 1,279 citations

Deletions of Chromosome 15 as a Cause of the Prader–Willi Syndrome

1981 • 615 citations

Prader‐Willi syndrome: Current understanding of cause and diagnosis

1990 • 574 citations

Prader-Willi syndrome

1984 • 200 citations

Every pediatrician a geneticist (1983): (With an evolutionary view of disease)

1984 • 150 citations

Food and Children With Prader-Willi Syndrome

1976 • 104 citations

Chromosome 1p terminal deletion: report of new findings and confirmation of two characteristic phenotypes.

1995 • 57 citations

Partial monosomy of chromosome 1p36.3: Characterization of the critical region and delineation of a syndrome

1995 • 53 citations

A variety of genetic mechanisms are associated with the Prader–Willi syndrome

1994 • 43 citations

The ascertainment and implications of an unbalanced translocation in the neonate. Familial 1:15 translocation

1980 • 38 citations

Clinical consequences of deletion 1p35.

1988 • 30 citations

The level of 6‐phosphogluconate dehydrogenase (6‐PGD) activity in a patient with a 1p terminal deletion suggests that the gene locus is not distal to sub‐band p36.3 on chromosome 1

1984 • 19 citations

Reciprocal translocation t(1;15)(p36.2;p11.2): Confirmation of a suggestive cytogenetic diagnosis by in situ hybridization and clinical case report on resulting monosomy (1p)

1992 • 18 citations

De novo translocation involving chromosomes 1 and 4 resulting in partial duplication of 4q and partial deletion of 1p

1994 • 13 citations

De novo deletion 1p(34?pter)

1985 • 12 citations