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Results: 6

Authors: COLLINET M BERTHELON M BENIT P LABORDE K DESBUQUOIS B MUNNICH A ROBERT JJ
Citation: M. Collinet et al., FAMILIAL HYPERPROINSULINAEMIA DUE TO A MUTATION SUBSTITUTING HISTIDINE FOR ARGININE AT POSITION-65 IN PROINSULIN - IDENTIFICATION OF THE MUTATION BY RESTRICTION ENZYME MAPPING, European journal of pediatrics, 157(6), 1998, pp. 456-460

Authors: ELGHOUZZI V LEMERRER M PERRINSCHMITT F LAJEUNIE E BENIT P RENIER D BOURGEOIS P BOLCATOBELLEMIN AL MUNNICH A BONAVENTURE J
Citation: V. Elghouzzi et al., MUTATIONS OF THE TWIST GENE IN THE SAETHRE-CHOTZEN SYNDROME, Nature genetics, 15(1), 1997, pp. 42-46

Authors: BENIT P REY F MELLE D MUNNICH A REY J
Citation: P. Benit et al., 5 NOVEL MISSENSE MUTATIONS OF THE PHENYLALANINE-HYDROXYLASE GENE IN PHENYLKETONURIA, Human mutation, 4(3), 1994, pp. 229-231

Authors: BENIT P REY F MELLE D MUNNICH A REY J
Citation: P. Benit et al., NOVEL FRAME-SHIFT DELETIONS OF THE PHENYLALANINE-HYDROXYLASE GENE IN PHENYLKETONURIA, Human molecular genetics, 3(4), 1994, pp. 675-676

Authors: SIMON M BENIT P VASSAL A DUBOIS C FAYE G
Citation: M. Simon et al., SEQUENCE OF THE PHO2-POL3 (CDC2) REGION OF CHROMOSOME-IV OF SACCHAROMYCES-CEREVISIAE, Yeast, 10(12), 1994, pp. 1653-1656

Authors: SERVILLE F BENIT P SAUGIER P VIBERT M ROYER G PELET A CHERY M MUNNICH A LYONNET S
Citation: F. Serville et al., PRENATAL EXCLUSION OF X-LINKED HYDROCEPHALUS STENOSIS OF THE AQUEDUCTOF SYLVIUS SEQUENCE USING CLOSELY LINKED DNA MARKERS, Prenatal diagnosis, 13(6), 1993, pp. 435-439
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