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Results: 1-25 | 26-49
Results: 1-25/49
LOCALIZATION OF THE GENE FOR A DOMINANT CONGENITAL SPINAL MUSCULAR-ATROPHY PREDOMINANTLY AFFECTING THE LOWER-LIMBS TO CHROMOSOME 12Q23-Q24
Authors: VANDERVLEUTEN AJW VANRAVENSWAAIJARTS CMA FRIJNS CJM SMITS APT HAGEMAN G PADBERG GW KREMER H
Citation: Ajw. Vandervleuten et al., LOCALIZATION OF THE GENE FOR A DOMINANT CONGENITAL SPINAL MUSCULAR-ATROPHY PREDOMINANTLY AFFECTING THE LOWER-LIMBS TO CHROMOSOME 12Q23-Q24, European journal of human genetics, 6(4), 1998, pp. 376-382
NON-ALLELIC GENETIC-HETEROGENEITY IN A FAMILY WITH NONSYNDROMAL DEAFNESS
Authors: KREMER H CREMERS CWRJ VANDENHELM B MARRES HAM MEERMAN GJT BLEIJS DA ROPERS HH MARIMAN ECM
Citation: H. Kremer et al., NON-ALLELIC GENETIC-HETEROGENEITY IN A FAMILY WITH NONSYNDROMAL DEAFNESS, European journal of human genetics, 6, 1998, pp. 4168-4168
EXCLUSION OF THE MYOSIN LIGHT-CHAIN-2 GENE AND THE RIBOSOMAL-PROTEIN L6 GENE FROM A CAUSATIVE ROLE IN THE PATHOGENESIS OF NOONAN-SYNDROME
Authors: KREMER H CROSBY AH VANREEN M KENMOCHI N ION A JAMIESON CR VANDERBURGT I PATTON MA MARIMAN ECM JEFFERY S
Citation: H. Kremer et al., EXCLUSION OF THE MYOSIN LIGHT-CHAIN-2 GENE AND THE RIBOSOMAL-PROTEIN L6 GENE FROM A CAUSATIVE ROLE IN THE PATHOGENESIS OF NOONAN-SYNDROME, European journal of human genetics, 6, 1998, pp. 4184-4184
THE ROLE OF THE TH-1 TO TH-2 SHIFT OF THE CYTOKINE PROFILES OF CD4 HELPER-CELLS IN THE PATHOGENESIS OF AUTOIMMUNE AND HYPERCATABOLIC DISEASES
Authors: HASSIG A KREMER H LIANG WX STAMPFLI K
Citation: A. Hassig et al., THE ROLE OF THE TH-1 TO TH-2 SHIFT OF THE CYTOKINE PROFILES OF CD4 HELPER-CELLS IN THE PATHOGENESIS OF AUTOIMMUNE AND HYPERCATABOLIC DISEASES, Medical hypotheses, 51(1), 1998, pp. 59-63
LOCALIZATION OF A GENE FOR NONSPECIFIC X-LINKED MENTAL-RETARDATION (MRX46) TO XQ25-Q26
Authors: YNTEMA HG HAMEL BCJ SMITS APT VANROOSMALEN T VANDENHELM B KREMER H ROPERS HH SMEETS DFCM VANBOKHOVEN H
Citation: Hg. Yntema et al., LOCALIZATION OF A GENE FOR NONSPECIFIC X-LINKED MENTAL-RETARDATION (MRX46) TO XQ25-Q26, Journal of Medical Genetics, 35(10), 1998, pp. 801-805
NATURALLY-OCCURRING TESTIS-SPECIFIC HISTONE H3 ANTISENSE TRANSCRIPTS IN DROSOPHILA
Authors: AKHMANOVA A KREMER H MIEDEMA K HENNIG W
Citation: A. Akhmanova et al., NATURALLY-OCCURRING TESTIS-SPECIFIC HISTONE H3 ANTISENSE TRANSCRIPTS IN DROSOPHILA, Molecular reproduction and development, 48(4), 1997, pp. 413-420
FURTHER DELINEATION OF THE CRITICAL REGION FOR NOONAN-SYNDROME ON THELONG ARM OF CHROMOSOME-12
Authors: BRADY AF JAMIESON CR VANDERBURGT I CROSBY A VANREEN M KREMER H MARIMAN E PATTON MA JEFFERY S
Citation: Af. Brady et al., FURTHER DELINEATION OF THE CRITICAL REGION FOR NOONAN-SYNDROME ON THELONG ARM OF CHROMOSOME-12, European journal of human genetics, 5(5), 1997, pp. 336-337
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
INDUCTION OF OVULATION WITH SEMINAL PLASMA IN GILTS - INVESTIGATION ON THE LOCAL SIGNAL-TRANSDUCTION
Authors: WABERSKI D HUNTER RHF KREMER H NETO GB JUNGBLUT PW KALLWEIT E WEITZE KF
Citation: D. Waberski et al., INDUCTION OF OVULATION WITH SEMINAL PLASMA IN GILTS - INVESTIGATION ON THE LOCAL SIGNAL-TRANSDUCTION, Reproduction in domestic animals, 32(1-2), 1997, pp. 10-10
FAMILIAL SPASTIC PARAPLEGIA - EVIDENCE FOR A 4TH LOCUS
Authors: BRUYN RPM VANVEEN MMM KREMER H SCHELTENS PH PADBERG GW
Citation: Rpm. Bruyn et al., FAMILIAL SPASTIC PARAPLEGIA - EVIDENCE FOR A 4TH LOCUS, Clinical neurology and neurosurgery, 99(2), 1997, pp. 87-90
A MEDICAL MYSTERY
Authors: KREMER H
Citation: H. Kremer, A MEDICAL MYSTERY, The New England journal of medicine, 336(12), 1997, pp. 846-846
FINE MAPPING OF THE GENE FOR AUTOSOMAL-DOMINANT CONGENITAL FACIAL PARALYSIS ON CHROMOSOME 3Q
Authors: PADBERG GW VANDERHELM B KUYT LP VANREEN M MARIMAN ECM KREMER H
Citation: Gw. Padberg et al., FINE MAPPING OF THE GENE FOR AUTOSOMAL-DOMINANT CONGENITAL FACIAL PARALYSIS ON CHROMOSOME 3Q, Neurology, 48(3), 1997, pp. 68001-68001
2 TYPES OF POLYADENATED MESSENGER-RNAS ARE SYNTHESIZED FROM DROSOPHILA REPLICATION-DEPENDENT HISTONE GENES
Authors: AKHMANOVA A MIEDEMA K KREMER H HENNIG W
Citation: A. Akhmanova et al., 2 TYPES OF POLYADENATED MESSENGER-RNAS ARE SYNTHESIZED FROM DROSOPHILA REPLICATION-DEPENDENT HISTONE GENES, European journal of biochemistry, 244(2), 1997, pp. 294-300
DIFFERENTIAL LOSS OF HETEROZYGOSITY IN THE REGION OF THE COWDEN LOCUSWITHIN 10Q22-23 IN FOLLICULAR THYROID ADENOMAS AND CARCINOMAS
Authors: MARSH DJ ZHENG ZM ZEDENIUS J KREMER H PADBERG GW LARSSON C LONGY M ENG C
Citation: Dj. Marsh et al., DIFFERENTIAL LOSS OF HETEROZYGOSITY IN THE REGION OF THE COWDEN LOCUSWITHIN 10Q22-23 IN FOLLICULAR THYROID ADENOMAS AND CARCINOMAS, Cancer research, 57(3), 1997, pp. 500-503
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 A CONGENITAL NONPROGRESSIVE SPINAL MUSCULAR-ATROPHY AFFECTING THE LOWER-LIMBS TO CHROMOSOME 12Q23-Q24
Authors: VANRAVENSWAAIJ CMA VANDERVLEUTEN AJW SMITS APT PADBERG GW KREMER H
Citation: Cma. Vanravenswaaij et al., LOCALIZATION OF THE GENE FOR A CONGENITAL NONPROGRESSIVE SPINAL MUSCULAR-ATROPHY AFFECTING THE LOWER-LIMBS TO CHROMOSOME 12Q23-Q24, American journal of human genetics, 61(4), 1997, pp. 1744-1744
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
ICHTHYOSIS BULLOSA OF SIEMENS - A DISTINCT TYPE OF EPIDERMOLYTIC HYPERKERATOSIS
Authors: LENZNER U HAPPLE R KREMER H MENSING H REINEL D STEIJLEN PM ULRICH R
Citation: U. Lenzner et al., ICHTHYOSIS BULLOSA OF SIEMENS - A DISTINCT TYPE OF EPIDERMOLYTIC HYPERKERATOSIS, EJD. European journal of dermatology, 6(3), 1996, pp. 164-167
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
LOCALIZATION OF A GENE FOR MOBIUS-SYNDROME TO CHROMOSOME 3Q BY LINKAGE ANALYSIS IN A DUTCH FAMILY
Authors: KREMER H KUYT LP VANDENHELM B VANREEN M LEUNISSEN JAM HAMEL BCJ JANSEN C MARIMAN ECM FRANTS RR PADBERG GW
Citation: H. Kremer et al., LOCALIZATION OF A GENE FOR MOBIUS-SYNDROME TO CHROMOSOME 3Q BY LINKAGE ANALYSIS IN A DUTCH FAMILY, Human molecular genetics, 5(9), 1996, pp. 1367-1371
OPTIMIZING THE COMBUSTION IN THE CALCINER OF A CEMENT PLANT
Authors: JESCHAR R JENNES R KREMER H KELLERHOFF T
Citation: R. Jeschar et al., OPTIMIZING THE COMBUSTION IN THE CALCINER OF A CEMENT PLANT, ZKG INTERNATIONAL, 49(6), 1996, pp. 304-317
LOCALIZATION OF THE GENE (OR GENES) FOR A SYNDROME WITH X-LINKED MENTAL-RETARDATION, ATAXIA, WEAKNESS, HEARING IMPAIRMENT, LOSS OF VISION AND A FATAL COURSE IN EARLY-CHILDHOOD
Authors: KREMER H HAMEL BCJ VANDENHELM B ARTS WFM DEWIJS IJ SISTERMANS EA ROPERS HH MARIMAN ECM
Citation: H. Kremer et al., LOCALIZATION OF THE GENE (OR GENES) FOR A SYNDROME WITH X-LINKED MENTAL-RETARDATION, ATAXIA, WEAKNESS, HEARING IMPAIRMENT, LOSS OF VISION AND A FATAL COURSE IN EARLY-CHILDHOOD, Human genetics, 98(5), 1996, pp. 513-517
GENETIC FINE MAPPING OF THE GENE FOR RECESSIVE STARGARDT DISEASE
Authors: HOYNG CB POPPELAARS F VANDEPOL TJR KREMER H PINCKERS AJLG DEUTMAN AF CREMERS FPM
Citation: Cb. Hoyng et al., GENETIC FINE MAPPING OF THE GENE FOR RECESSIVE STARGARDT DISEASE, Human genetics, 98(4), 1996, pp. 500-504
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
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
Risultati: 1-25 | 26-49