Authors: VERKARRE V FOURNET JC DELONLAY P RAHIER J ROBERT JJ NIHOULFEKETE C

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Authors: DELONLAY P FOURNET JC VERKARRE V RAHIER J JUNIEN C NIHOULFEKETE C ROBERT JJ SAUDUBRAY JM

Citation: P. Delonlay et al., SYNDROME OF CONGENITAL HYPERINSULINISM AND HYPERAMMONEMIA IN 6 UNRELATED PATIENTS, European journal of human genetics, 6, 1998, pp. 1105-1105

Authors: DELONLAY P FOURNET JC VERKARRE V RAHIER J ROBERT JJ NIHOULFEKETE C SAUDUBRAY JM JUNIEN C

Citation: P. Delonlay et al., PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY (PHHI) IS A HETEROGENEOUS DISORDER WITH 2 HISTOLOGICAL FORMS AND DIFFERENT MOLECULAR-BASIS, European journal of human genetics, 6, 1998, pp. 1108-1108

Authors: VERKARRE V FOURNET JC DELONLAY P GROSSMORAND MS DEVILLERS M RAHIER J BRUNELLE F ROBERT JJ NIHOULFEKUTE C SAUDUBRAY JM JUNIEN C

Citation: V. Verkarre et al., PATERNAL MUTATION OF THE SULFONYLUREA RECEPTOR (SUR1) GENE AND MATERNAL LOSS OF 11P15 IMPRINTED GENES LEAD TO PERSISTENT HYPERINSULINISM INFOCAL ADENOMATOUS HYPERPLASIA, The Journal of clinical investigation, 102(7), 1998, pp. 1286-1291

Authors: DELONLAY P FOURNET JC VERKARRE V RAHIER J GROSSMORAND MS BRUNELLE F ROBERT JJ NIHOULFEKETE C SAUDUBRAY JM JUNIEN C

Citation: P. Delonlay et al., SOMATIC DELETION OF THE IMPRINTED 11P15 REGION IN SPORADIC PERSISTENTHYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY IS SPECIFIC OF FOCAL ADENOMATOUS HYPERPLASIA, American journal of human genetics, 61(4), 1997, pp. 198-198