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BMJ Case Reports|July 7, 2011

Isolated imprinting mutation of the DLK1/GTL2 locus associated with a clinical presentation of maternal uniparental disomy of chromosome 14I K Temple, V Shrubb, M Lever, et al.

Journal of Medical Genetics|July 3, 2007

Isolated imprinting mutation of the DLK1/GTL2 locus associated with a clinical presentation of maternal uniparental disomy of chromosome 14I K Temple, V Shrubb, M Lever, et al.

Disability and Rehabilitation|July 14, 2001

Opinion statement on the minimal acceptable standards of healthcare in cerebral palsyA M Bakheit, E Bower, A Cosgrove, et al.

Cytogenetic and Genome Research|July 21, 2009

Constitutional haploinsufficiency of tumor suppressor genes in mentally retarded patients with microdeletions in 17p13.1A C V Krepischi-Santos, D Rajan, I K Temple, et al.

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Showing results (1-10 of 4) with videos related to

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Pageof 1

BMJ Case Reports|July 7, 2011

Isolated imprinting mutation of the DLK1/GTL2 locus associated with a clinical presentation of maternal uniparental disomy of chromosome 14I K Temple, V Shrubb, M Lever, et al.

Journal of Medical Genetics|July 3, 2007

Isolated imprinting mutation of the DLK1/GTL2 locus associated with a clinical presentation of maternal uniparental disomy of chromosome 14I K Temple, V Shrubb, M Lever, et al.

Disability and Rehabilitation|July 14, 2001

Opinion statement on the minimal acceptable standards of healthcare in cerebral palsyA M Bakheit, E Bower, A Cosgrove, et al.

Cytogenetic and Genome Research|July 21, 2009

Constitutional haploinsufficiency of tumor suppressor genes in mentally retarded patients with microdeletions in 17p13.1A C V Krepischi-Santos, D Rajan, I K Temple, et al.

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