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

Data up to Jan 2025

Published1981
Citations615
References17

Total Citations Per Year

Abstract

References (17)

RADIOGRAPHIC ATLAS OF SKELETAL DEVELOPMENT OF THE HAND AND WRIST

1959 • 5,245 citations

Localization of heterochromatin in human chromosomes

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Wilkins the Diagnosis and Treatment of Endocrine Disorders in Childhood and Adolescence

1994 • 919 citations

Aniridia-Wilms’ tumor association: evidence for specific deletion of 11p13

1979 • 404 citations

Quantitative analysis of high-resolution trypsin-Giemsa bands on human prometaphase chromosomes

1978 • 248 citations

Prader-Willi syndrome

1972 • 207 citations

The aniridia-Wilms tumor association: The critical role of chromosome band 11p13

1980 • 123 citations

The association of chromosome 3 duplication and the Correlia de Lange syndrome

1978 • 80 citations

The Prader-Willi syndrome with a 15/15 translocation. Case report and review of the literature.

1976 • 79 citations

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1979 • 46 citations

15/15 translocation in Prader-Willi syndrome.

1977 • 45 citations

Translocation between both members of chromosome pair number 15 causing recurrent abortions

1969 • 32 citations

Prader‐Willi syndrome and chromosomal mosaicism 46, XY/47, XY, + mar in two cases

1979 • 28 citations

De novo 13q paracentric inversion in a boy with cleft palate and mental retardation

1979 • 27 citations

A CASE OF PRADER‐WILLI SYNDROME IN A GIRL WITH A SMALL EXTRA CHROMOSOME

1971 • 26 citations

Chromosome 15 and Prader‐Willi Syndrome

1978 • 23 citations

Translocation D/D involving two homologous chromosomes of the pair 15

1977 • 14 citations

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