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Results: 1-7 |
Results: 7
GERMLINE MUTATIONS IN THE PTEN MMAC1 GENE IN PATIENTS WITH COWDEN-DISEASE/
Authors: NELEN MR VANSTAVEREN WCG PEETERS EAJ BENHASSEL M GORLIN RJ HAMM H LINDBOE CF FRYNS JP SIJMONS RH WOODS DG MARIMAN ECM PADBERG GW KREMER H
Citation: Mr. Nelen et al., GERMLINE MUTATIONS IN THE PTEN MMAC1 GENE IN PATIENTS WITH COWDEN-DISEASE/, Human molecular genetics, 6(8), 1997, pp. 1383-1387
IDENTIFICATION OF PTEN MMAC1 GERMLINE MUTATIONS IN COWDEN-DISEASE PATIENTS/
Authors: NELEN MR VANSTAVEREN W PEETERS E HASSEL M GORLIN R HAMM H LINBOE C FRYNS J SIJMONS R WOODS D MARINAN E PADBERG G KREMER H
Citation: Mr. Nelen et al., IDENTIFICATION OF PTEN MMAC1 GERMLINE MUTATIONS IN COWDEN-DISEASE PATIENTS/, American journal of human genetics, 61(4), 1997, pp. 414-414
LOCALIZATION OF THE GENE FOR COWDEN DISEASE TO CHROMOSOME 10Q22-23
Authors: NELEN MR PADBERG GW PEETERS EAJ LIN AY VANDENHELM B FRANTS RR COULON V GOLDSTEIN AM VANREEN MMM EASTON DF EELES RA HODGSON S MULVIHILL JJ MURDAY VA TUCKER MA MARIMAN ECM STARINK TM PONDER BAJ ROPERS HH KREMER H LONGY M ENG C
Citation: Mr. Nelen et al., LOCALIZATION OF THE GENE FOR COWDEN DISEASE TO CHROMOSOME 10Q22-23, Nature genetics, 13(1), 1996, pp. 114-116
IN ORGANELLO FOOTPRINT ANALYSIS OF HUMAN MITOCHONDRIAL-DNA - HUMAN MITOCHONDRIAL TRANSCRIPTION FACTOR-A INTERACTIONS AT THE ORIGIN OF REPLICATION
Authors: GHIVIZZANI SC MADSEN CS NELEN MR AMMINI CV HAUSWIRTH WW
Citation: Sc. Ghivizzani et al., IN ORGANELLO FOOTPRINT ANALYSIS OF HUMAN MITOCHONDRIAL-DNA - HUMAN MITOCHONDRIAL TRANSCRIPTION FACTOR-A INTERACTIONS AT THE ORIGIN OF REPLICATION, Molecular and cellular biology, 14(12), 1994, pp. 7717-7730
FAMILIAL ANGELMAN SYNDROME WITH A CROSSOVER IN THE CRITICAL DELETION REGION
Authors: NELEN MR VANDERBURGT CJAM NILLESEN WN VIS A SMEETS HJM
Citation: Mr. Nelen et al., FAMILIAL ANGELMAN SYNDROME WITH A CROSSOVER IN THE CRITICAL DELETION REGION, American journal of medical genetics, 52(3), 1994, pp. 352-357
IDENTIFICATION OF 4 NOVEL MUTATIONS IN THE COL4A5 GENE OF PATIENTS WITH ALPORT SYNDROME
Authors: LEMMINK HH SCHRODER CH BRUNNER HG NELEN MR ZHOU J TRYGGVASON K HAAGSMASCHOUTEN WAG ROODVOETS AP RASCHER W VANOOST BA SMEETS HJM
Citation: Hh. Lemmink et al., IDENTIFICATION OF 4 NOVEL MUTATIONS IN THE COL4A5 GENE OF PATIENTS WITH ALPORT SYNDROME, Genomics, 17(2), 1993, pp. 485-489
X-LINKED BORDERLINE MENTAL-RETARDATION WITH PROMINENT BEHAVIORAL DISTURBANCE - PHENOTYPE, GENETIC LOCALIZATION, AND EVIDENCE FOR DISTURBED MONOAMINE METABOLISM
Authors: BRUNNER HG NELEN MR VANZANDVOORT P ABELING NGGM VANGENNIP AH WOLTERS EC KUIPER MA ROPERS HH VANOOST BA
Citation: Hg. Brunner et al., X-LINKED BORDERLINE MENTAL-RETARDATION WITH PROMINENT BEHAVIORAL DISTURBANCE - PHENOTYPE, GENETIC LOCALIZATION, AND EVIDENCE FOR DISTURBED MONOAMINE METABOLISM, American journal of human genetics, 52(6), 1993, pp. 1032-1039
Risultati: 1-7 |