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Publications by J O van Hemel

Linkage Analysis With Chromosome 15q11-13 Markers Shows Genomic Imprinting in Familial Angelman Syndrome.

Journal of Medical Genetics

English

Related publications

Common Genetic Variation in the Angelman Syndrome Imprinting Centre Affects the Imprinting of Chromosome 15

European Journal of Human Genetics

English

Prader-Willi, Angelman, and 15q11-Q13 Duplication Syndromes

Pediatric Clinics of North America

English

A Putative Gene Family in 15q11-13 and 16p11.2: Possible Implications for Prader-Willi and Angelman Syndromes.

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

English

Microarray Based Comparative Genomic Hybridization Testing in Deletion Bearing Patients With Angelman Syndrome: Genotype-Phenotype Correlations

Journal of Medical Genetics

English

Parental Origin Effects in Human Trisomy for Chromosome 14q: Implications for Genomic Imprinting.

Journal of Medical Genetics

English

Mutation Analysis of UBE3A in Angelman Syndrome Patients

American Journal of Human Genetics

English

Oguchi Disease: Suggestion of Linkage to Markers on Chromosome 2q.

Journal of Medical Genetics

English

High-Density Genome Scan in Crohn Disease Shows Confirmed Linkage to Chromosome 14q11-12

American Journal of Human Genetics

English

Genomic Imprinting in Marsupial Placentation

Reproductive Medicine

English