Searchable abstracts of presentations at key conferences in endocrinology

Endocrine Abstracts

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8th European Congress of Endocrinology incorporating the British Endocrine Societies

Oral Communications

Endocrine genetics

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Neuroendocrinology and neoplasia
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Calcium and bone OC49 Novartis Oncology Young Investigator Award

ea0011oc41 | Endocrine genetics

Mutations in Cullin 7, a cofactor for Ubiquitination, cause the 3M intra-uterine growth retardation syndrome

ea0011oc42 | Endocrine genetics

Linkage of a fourth gene for familial glucocorticoid deficiency to chromosome 13q

ea0011oc43 | Endocrine genetics

Mutation screening of SLC26A4 (PDS) gene in patients with Pendred syndrome and nonsyndromic enlarged vestibular aqueduct

ea0011oc44 | Endocrine genetics

Functional impact of polymorphic variation in the gene encoding 11β-hydroxylase (CYP11B1): reduced adrenal 11-hydroxylase efficiency identifies a key intermediate phenotype in hypertension

ea0011oc45 | Endocrine genetics

Genotype/phenotype correlation of PRKAR1A mutations in patients with Carney complex (CNC) and/or sporadic primary pigmented nodular adrenocortical disease (PPNAD) from the CNC network

ea0011oc46 | Endocrine genetics

Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC-gene

ea0011oc47 | Endocrine genetics

Frequent involvement of BMP15 gene variants in women with premature ovarian failure

ea0011oc48 | Endocrine genetics

Progressive osseous heteroplasia: a phenotype associated with mutations of the GNAS1 gene

Published by BioScientifica

Endocrine Abstracts
ISSN 1470-3947 (print) | ISSN 1479-6848 (online)
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