Paternal deletion of the GNAS imprinted locus (including Gnasxl) in two girls presenting with severe pre- and post-natal growth retardation and intractable feeding difficulties

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Paternal deletion of the GNAS imprinted locus (including Gnasxl) in two girls presenting with severe pre- and post-natal growth retardation and intractable feeding difficulties

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Edité par CCSD ; Nature Publishing Group -

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Paternal deletion of the GNAS imprinted locus (including Gnasxl) in two girls presenting with severe pre- and post-natal growth retardation and intractable feeding difficulties

Consulter en ligne

Suggestions

Du même auteur

Cryptic terminal deletion of chromosome 9q34: a novel cause of syndromic obesity in childhood?

Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders.

Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype.

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Paternal deletion of the GNAS imprinted locus (including Gnasxl) in two girls presenting with severe pre- and post-natal growth retardation and intractable feeding difficulties

Consulter en ligne

Suggestions

Du même auteur

Cryptic terminal deletion of chromosome 9q34: a novel cause of syndromic obesity in childhood?

Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders.

Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype.

Liens utiles

Coordonnées