The human chromosomal gene for necdin, a neuronal growth suppressor, in the Prader-Willi syndrome deletion region

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Elsevier

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C11orf21, a novel gene within the Beckwith-Wiedemann syndrome region in human chromosome 11p15.5

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Prader-Willi Syndrome: Obesity due to Genomic Imprinting

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Identification of a putative DNA replication origin in the -aminobutyric acid receptor subunit 3 and 5 gene cluster on human chromosome 15q11-q13, a region associated with parental imprinting and allele-specific replication timing

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A 1.5-Mb Physical Map of the Hidrotic Ectodermal Dysplasia (Clouston Syndrome) Gene Region on Human Chromosome 13q11

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