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Results: 1-11 |
Results: 11
GENETIC AND ENVIRONMENTAL RISK-FACTORS IN PARKINSONS-DISEASE
Authors: VELDMAN BAJ WIJN AM KNOERS N PRAAMSTRA P HORSTINK MWIM
Citation: Baj. Veldman et al., GENETIC AND ENVIRONMENTAL RISK-FACTORS IN PARKINSONS-DISEASE, Clinical neurology and neurosurgery, 100(1), 1998, pp. 15-26
CHARACTERIZATION OF THE GENE ENCODING HUMAN SARCOLIPIN (SLN), A PROTEOLIPID ASSOCIATED WITH SERCA1 - ABSENCE OF STRUCTURAL MUTATIONS IN 5 PATIENTS WITH BRODY-DISEASE
Authors: ODERMATT A TASCHNER PEM SCHERER SW BEATTY B KHANNA VK CORNBLATH DR CHAUDHRY V YEE WC SCHRANK B KARPATI G BREUNING MH KNOERS N MACLENNAN DH
Citation: A. Odermatt et al., CHARACTERIZATION OF THE GENE ENCODING HUMAN SARCOLIPIN (SLN), A PROTEOLIPID ASSOCIATED WITH SERCA1 - ABSENCE OF STRUCTURAL MUTATIONS IN 5 PATIENTS WITH BRODY-DISEASE, Genomics, 45(3), 1997, pp. 541-553
GENETIC-LINKAGE OF 2 DIFFERENT PHENOTYPES OF ROD AND CONE DYSTROPHY IN A FAMILY WITH PSEUDO-DOMINANT INHERITANCE TO 1P21-P13
Authors: HOYNG CB DEUTMAN AF VANDEPOL D KNOERS N PINCKERS A CREMERS FPM
Citation: Cb. Hoyng et al., GENETIC-LINKAGE OF 2 DIFFERENT PHENOTYPES OF ROD AND CONE DYSTROPHY IN A FAMILY WITH PSEUDO-DOMINANT INHERITANCE TO 1P21-P13, Investigative ophthalmology & visual science, 38(4), 1997, pp. 3690-3690
REFINEMENT OF THE LOCUS FOR THE NAIL-PATELLA SYNDROME AT 9Q34
Authors: HOL FA GEURDS MPA MARIMAN ECM KNOERS N
Citation: Fa. Hol et al., REFINEMENT OF THE LOCUS FOR THE NAIL-PATELLA SYNDROME AT 9Q34, American journal of human genetics, 61(4), 1997, pp. 1627-1627
LINKAGE ANALYSIS IN A FAMILY WITH PSEUDO-DOMINANTLY INHERITED CONE-ROD DYSTROPHY AND RETINITIS-PIGMENTOSA SUGGESTS THAT THE DEFECTS RESIDE IN THE STARGARDT-DISEASE GENE ABCR
Authors: CREMERS F VANDEPOL D ROZET JM GERBER S VANHAREN F TIJMES N BLANKENAGEL A BERGEN A KNOERS N KREMER H DAHL N PINCKERS A DEUTMAN A KAPLAN J HOYNG C
Citation: F. Cremers et al., LINKAGE ANALYSIS IN A FAMILY WITH PSEUDO-DOMINANTLY INHERITED CONE-ROD DYSTROPHY AND RETINITIS-PIGMENTOSA SUGGESTS THAT THE DEFECTS RESIDE IN THE STARGARDT-DISEASE GENE ABCR, American journal of human genetics, 61(4), 1997, pp. 1930-1930
X-LINKED MENTAL-RETARDATION - RESULTS OF A COMBINED CLINICAL, CYTOGENETIC AND MOLECULAR APPROACH
Authors: HAMEL BCJ SMEETS DFCM SMITS APT VANDENHELM B KREMER H KNOERS N ROPERS HH MARIMAN EC
Citation: Bcj. Hamel et al., X-LINKED MENTAL-RETARDATION - RESULTS OF A COMBINED CLINICAL, CYTOGENETIC AND MOLECULAR APPROACH, American journal of medical genetics, 64(1), 1996, pp. 19-19
X-LINKED MENTAL-RETARDATION - THE NIJMEGEN EXPERIENCE - HIGHLIGHTS AND PITFALLS
Authors: HAMEL BCJ SMEETS DFCM SMITS APT VANDENHELM B KREMER H KNOERS N ROPER HH MARIMAN EC
Citation: Bcj. Hamel et al., X-LINKED MENTAL-RETARDATION - THE NIJMEGEN EXPERIENCE - HIGHLIGHTS AND PITFALLS, American journal of medical genetics, 64(1), 1996, pp. 19-19
ABERRANT PROTEOGLYCAN COMPOSITION OF THE GLOMERULAR-BASEMENT-MEMBRANEIN A PATIENT WITH DENYS-DRASH SYNDROME
Authors: VANDENHEUVEL LP WESTENEND PJ VANDENBORN J KNOERS N ASSMANN KJM MONNENS LAH
Citation: Lp. Vandenheuvel et al., ABERRANT PROTEOGLYCAN COMPOSITION OF THE GLOMERULAR-BASEMENT-MEMBRANEIN A PATIENT WITH DENYS-DRASH SYNDROME, Kidney international, 50(5), 1996, pp. 1813-1813
ABERRANT PROTEOGLYCAN COMPOSITION OF THE GLOMERULAR-BASEMENT-MEMBRANEIN A PATIENT WITH DENYS-DRASH SYNDROME
Authors: VANDENHEUVEL LPWJ WESTENEND PJ VANDENBORN J ASSMANN KJM KNOERS N MONNENS LAH
Citation: Lpwj. Vandenheuvel et al., ABERRANT PROTEOGLYCAN COMPOSITION OF THE GLOMERULAR-BASEMENT-MEMBRANEIN A PATIENT WITH DENYS-DRASH SYNDROME, Nephrology, dialysis, transplantation, 10(12), 1995, pp. 2205-2211
ABERRANT PROTEOGLYCAN COMPOSITION OF THE GLOMERULAR-BASEMENT-MEMBRANEIN A PATIENT WITH DENYS-DRASH SYNDROME
Authors: VANDENHEUVEL LP WESTENEND PJ VANDENBORN J KNOERS N ASSMANN KJM SCHRODER CH MONNENS LAH
Citation: Lp. Vandenheuvel et al., ABERRANT PROTEOGLYCAN COMPOSITION OF THE GLOMERULAR-BASEMENT-MEMBRANEIN A PATIENT WITH DENYS-DRASH SYNDROME, Journal of the American Society of Nephrology, 5(3), 1994, pp. 653-653
NEPHROGENIC DIABETES-INSIPIDUS - IDENTIFICATION OF THE GENETIC-DEFECT
Authors: KNOERS N VONDEROUWELAND A DREESEN J VERDIJK M MONNENS LAH VONOOST BA
Citation: N. Knoers et al., NEPHROGENIC DIABETES-INSIPIDUS - IDENTIFICATION OF THE GENETIC-DEFECT, Pediatric nephrology, 7(5), 1993, pp. 685-688
Risultati: 1-11 |