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    1. Tartaglia, M; Mehler, EL; Goldberg, R; Zampino, G; Brunner, HG; Kremer, H; van der Burgt, I; Crosby, AH; Ion, A; Jeffery, S; Kalidas, K; Patton, MA; Kucherlapati, RS; Gelb, BD
      Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

      NATURE GENETICS
    2. Tartaglia, M; Mehler, EL; Goldberg, R; Zampino, G; Brunner, HG; Kremer, H; van der Burgt, I; Crosby, AH; Ion, A; Jeffery, S; Kalidas, K; Patton, MA; Kucherlapati, RS; Gelb, B
      Mutations in the protein tyrosine kinase gene, PTPN11, cause Noonan Syndrome (vol 29, pg 465, 2001)

      NATURE GENETICS
    3. Weigel, MM; Kremer, H; Sonnenberg-Schwan, U; Golz, J; Gurtler, L; Doerr, HW; Brockmeyer, NH
      Diagnostics and treatment of HIV-discordant couples who wish to have children

      EUROPEAN JOURNAL OF MEDICAL RESEARCH
    4. Kremer, H; May, F; Wirtz, S
      The influence of furnace design on the NO formation in high temperature processes

      ENERGY CONVERSION AND MANAGEMENT
    5. Kremer, H
      Der 'Schrecken'

      LITERATUR UND KRITIK
    6. Scherello, A; Flamme, M; Kremer, H
      Optimization of burner systems for glass melting furnaces with regenerative air preheating

      GLASS SCIENCE AND TECHNOLOGY-GLASTECHNISCHE BERICHTE
    7. Hargrave, M; James, K; Nield, K; Toomes, C; Georgas, K; Sullivan, T; Verzijl, HTFM; Oley, CA; Little, M; De Jonghe, P; Kwon, JM; Kremer, H; Dixon, MJ; Tirnmerman, V; Yamada, T; Koopman, P
      Fine mapping of the neurally expressed gene SOX14 to human 3q23, relative to three congenital diseases

      HUMAN GENETICS
    8. Jeuken, JWM; Nelen, MR; Vermeer, H; van Staveren, WCG; Kremer, H; van Overbeeke, JJ; Boerman, RH
      PTEN mutation analysis in two genetic subtypes of high-grade oligodendroglial tumors: PTEN is only occasionally mutated in one of the two genetic subtypes

      CANCER GENETICS AND CYTOGENETICS
    9. Ion, A; Crosby, AH; Kremer, H; Kenmochi, N; Van Reen, M; Fenske, C; Van der Burgt, I; Brunner, HG; Montgomery, K; Kucherlapati, RS; Patton, MA; Page, DC; Mariman, E; Jeffery, S
      Detailed mapping, mutation analysis, and intragenic polymorphism identification in candidate Noonan syndrome genes MYL2, DCN, EPS8, and RPL6

      JOURNAL OF MEDICAL GENETICS
    10. van Alfen, N; van Engelen, BGM; Reinders, JWC; Kremer, H; Gabreels, FJM
      The natural history of hereditary neuralgic amyotrophy in the Dutch population - Two distinct types?

      BRAIN
    11. Nelen, MR; Kremer, H; Konings, IBM; Schoute, F; van Essen, AJ; Koch, R; Woods, CG; Fryns, JP; Hamel, B; Hoefsloot, LH; Peeters, EAJ; Padberg, GW
      Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlations

      EUROPEAN JOURNAL OF HUMAN GENETICS
    12. Jeschar, R; Jennes, R; Kremer, H; Kellerhoff, T
      Reducing NOx and CO emissions by burning plastics in the calciner of a rotary cement kiln plant

      ZKG INTERNATIONAL
    13. May, F; Kremer, H
      Mathematical modelling of glass melting furnace design with regard to NOx formation

      GLASTECHNISCHE BERICHTE-GLASS SCIENCE AND TECHNOLOGY
    14. van de Wetering, RAC; Gabreels-Festen, AAWM; Kremer, H; Kalscheuer, VM; Gabreels, FJM; Mariman, EC
      Regulation and expression of the murine Pmp22 gene

      MAMMALIAN GENOME
    15. Waberski, D; Kremer, H; Neto, GB; Jungblut, PW; Kallweit, E; Weitze, KF
      Studies on a local effect of boar seminal plasma on ovulation time in gilts

      JOURNAL OF VETERINARY MEDICINE SERIES A-PHYSIOLOGY PATHOLOGY CLINICAL MEDICINE
    16. Kremer, H; Lilienthal, H; Hany, J; Roth-Harer, A; Winneke, G
      Sex-dependent effects of maternal PCB exposure on the electroretinogram inadult rats

      NEUROTOXICOLOGY AND TERATOLOGY
    17. Siderius, LE; Hamel, BCJ; van Bokhoven, H; de Jager, F; van den Helm, B; Kremer, H; Heineman-de Boer, JA; Ropers, HH; Mariman, ECM
      X-linked mental retardation associated with cleft lip palate maps to Xp11.3-q21.3

      AMERICAN JOURNAL OF MEDICAL GENETICS
    18. des Portes, V; Beldjord, C; Chelly, J; Hamel, B; Kremer, H; Smits, A; van Bokhoven, H; Ropers, HH; Claes, S; Fryns, JP; Ronce, N; Gendrot, C; Toutain, A; Raynaud, M; Moraine, C
      X-linked nonspecific mental retardation (MRX) linkage studies in 25 unrelated families: The European XLMR Consortium

      AMERICAN JOURNAL OF MEDICAL GENETICS
    19. Hamel, BCJ; Smits, APT; van den Helm, B; Smeets, DFCM; Knoers, NVAM; van Roosmalen, T; Thoonen, GHJ; Assman-Hulsmans, CFCH; Ropers, HH; Mariman, ECM; Kremer, H
      Four families (MRX43, MRX44, MRX45, MRX52) with nonspecific X-linked mental retardation: Clinical and psychometric data and results of linkage analysis

      AMERICAN JOURNAL OF MEDICAL GENETICS
    20. Yntema, HG; van den Helm, B; Knoers, NVAM; Smits, APT; van Roosmalen, T; Smeets, DFCM; Mariman, ECM; van der Burgt, I; van Bokhoven, H; Ropers, HH; Kremer, H; Hamel, BCJ
      X-linked mental retardation: Evidence for a recent mutation in a five-generation family (MRX65) linked to the pericentromeric region

      AMERICAN JOURNAL OF MEDICAL GENETICS
    21. Hamel, BCJ; Wesseling, P; Renier, WO; van den Helm, B; Ropers, HH; Kremer, H; Mariman, ECM
      A new X linked neurodegenerative syndrome with metal retardation, blindness, convulsions, spasticity, mild hypomyelination, and early death maps to the pericentromeric region (vol 36, pg 140, 1999)

      JOURNAL OF MEDICAL GENETICS
    22. Hamel, BCJ; Wesseling, P; Renier, WO; van den Helm, B; Ropers, HH; Kremer, H; Mariman, ECM
      A new X linked neurodegenerative syndrome with mental retardation, blindness, convulsions, spasticity, mild hypomyelination, and early death maps to the pericentromeric region

      JOURNAL OF MEDICAL GENETICS
    23. Kremer, H; Martens, JWM; van Reen, M; Verhoef-Post, M; Wit, JM; Otten, BJ; Drop, SLS; Delemarre-van de Waal, HA; Pombo-Arias, M; De Luca, F; Potau, N; Buckler, JMH; Jansen, M; Parks, JS; Latif, HA; Moll, GW; Epping, W; Saggese, G; Mariman, ECM; Themmen, APN; Brunner, HG
      A limited repertoire of mutations of the luteinizing hormone (LH) receptorgene in familial and sporadic patients with male LH-independent precociouspuberty

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    24. Verzijl, HTFM; van den Helm, B; Veldman, B; Hamel, BCJ; Kuyt, LP; Padberg, GW; Kremer, H
      A second gene for autosomal dominant Mobius syndrome is localized to chromosome 10q, in a Dutch family

      AMERICAN JOURNAL OF HUMAN GENETICS
    25. van Steensel, M; Smith, FJD; Steijlen, PM; Kluijt, I; Stevens, HP; Messenger, A; Kremer, H; Dunnill, MGS; Kennedy, C; Munro, CS; Doherty, VR; McGrath, JA; Covello, SP; Coleman, CM; Uitto, J; McLean, WHI
      The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: Exclusion of the hr gene by cDNA and genomic sequencing

      AMERICAN JOURNAL OF HUMAN GENETICS
    26. VANDERVLEUTEN AJW; VANRAVENSWAAIJARTS CMA; FRIJNS CJM; SMITS APT; HAGEMAN G; PADBERG GW; KREMER H
      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
    27. KREMER H; CREMERS CWRJ; VANDENHELM B; MARRES HAM; MEERMAN GJT; BLEIJS DA; ROPERS HH; MARIMAN ECM
      NON-ALLELIC GENETIC-HETEROGENEITY IN A FAMILY WITH NONSYNDROMAL DEAFNESS

      European journal of human genetics
    28. KREMER H; CROSBY AH; VANREEN M; KENMOCHI N; ION A; JAMIESON CR; VANDERBURGT I; PATTON MA; MARIMAN ECM; JEFFERY S
      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
    29. HASSIG A; KREMER H; LIANG WX; STAMPFLI K
      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
    30. YNTEMA HG; HAMEL BCJ; SMITS APT; VANROOSMALEN T; VANDENHELM B; KREMER H; ROPERS HH; SMEETS DFCM; VANBOKHOVEN H
      LOCALIZATION OF A GENE FOR NONSPECIFIC X-LINKED MENTAL-RETARDATION (MRX46) TO XQ25-Q26

      Journal of Medical Genetics
    31. Kremer, H; Lavrijsen, APM; McLean, WHI; Lane, EB; Melchers, D; Ruiter, DJ; Mariman, ECM; Steijlen, PM
      An atypical form of bullous congenital ichthyosiform erythroderma is caused by a mutation in the L12 linker region of keratin 1

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    32. AKHMANOVA A; KREMER H; MIEDEMA K; HENNIG W
      NATURALLY-OCCURRING TESTIS-SPECIFIC HISTONE H3 ANTISENSE TRANSCRIPTS IN DROSOPHILA

      Molecular reproduction and development
    33. BRADY AF; JAMIESON CR; VANDERBURGT I; CROSBY A; VANREEN M; KREMER H; MARIMAN E; PATTON MA; JEFFERY S
      FURTHER DELINEATION OF THE CRITICAL REGION FOR NOONAN-SYNDROME ON THELONG ARM OF CHROMOSOME-12

      European journal of human genetics
    34. 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
      GERMLINE MUTATIONS IN THE PTEN MMAC1 GENE IN PATIENTS WITH COWDEN-DISEASE/

      Human molecular genetics
    35. WABERSKI D; HUNTER RHF; KREMER H; NETO GB; JUNGBLUT PW; KALLWEIT E; WEITZE KF
      INDUCTION OF OVULATION WITH SEMINAL PLASMA IN GILTS - INVESTIGATION ON THE LOCAL SIGNAL-TRANSDUCTION

      Reproduction in domestic animals
    36. BRUYN RPM; VANVEEN MMM; KREMER H; SCHELTENS PH; PADBERG GW
      FAMILIAL SPASTIC PARAPLEGIA - EVIDENCE FOR A 4TH LOCUS

      Clinical neurology and neurosurgery
    37. KREMER H
      A MEDICAL MYSTERY

      The New England journal of medicine
    38. PADBERG GW; VANDERHELM B; KUYT LP; VANREEN M; MARIMAN ECM; KREMER H
      FINE MAPPING OF THE GENE FOR AUTOSOMAL-DOMINANT CONGENITAL FACIAL PARALYSIS ON CHROMOSOME 3Q

      Neurology
    39. AKHMANOVA A; MIEDEMA K; KREMER H; HENNIG W
      2 TYPES OF POLYADENATED MESSENGER-RNAS ARE SYNTHESIZED FROM DROSOPHILA REPLICATION-DEPENDENT HISTONE GENES

      European journal of biochemistry
    40. MARSH DJ; ZHENG ZM; ZEDENIUS J; KREMER H; PADBERG GW; LARSSON C; LONGY M; ENG C
      DIFFERENTIAL LOSS OF HETEROZYGOSITY IN THE REGION OF THE COWDEN LOCUSWITHIN 10Q22-23 IN FOLLICULAR THYROID ADENOMAS AND CARCINOMAS

      Cancer research
    41. 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
      IDENTIFICATION OF PTEN MMAC1 GERMLINE MUTATIONS IN COWDEN-DISEASE PATIENTS/

      American journal of human genetics
    42. VANRAVENSWAAIJ CMA; VANDERVLEUTEN AJW; SMITS APT; PADBERG GW; KREMER H
      LOCALIZATION OF THE GENE FOR A CONGENITAL NONPROGRESSIVE SPINAL MUSCULAR-ATROPHY AFFECTING THE LOWER-LIMBS TO CHROMOSOME 12Q23-Q24

      American journal of human genetics
    43. 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
      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
    44. LENZNER U; HAPPLE R; KREMER H; MENSING H; REINEL D; STEIJLEN PM; ULRICH R
      ICHTHYOSIS BULLOSA OF SIEMENS - A DISTINCT TYPE OF EPIDERMOLYTIC HYPERKERATOSIS

      EJD. European journal of dermatology
    45. 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
      LOCALIZATION OF THE GENE FOR COWDEN DISEASE TO CHROMOSOME 10Q22-23

      Nature genetics
    46. KREMER H; KUYT LP; VANDENHELM B; VANREEN M; LEUNISSEN JAM; HAMEL BCJ; JANSEN C; MARIMAN ECM; FRANTS RR; PADBERG GW
      LOCALIZATION OF A GENE FOR MOBIUS-SYNDROME TO CHROMOSOME 3Q BY LINKAGE ANALYSIS IN A DUTCH FAMILY

      Human molecular genetics
    47. JESCHAR R; JENNES R; KREMER H; KELLERHOFF T
      OPTIMIZING THE COMBUSTION IN THE CALCINER OF A CEMENT PLANT

      ZKG INTERNATIONAL
    48. KREMER H; HAMEL BCJ; VANDENHELM B; ARTS WFM; DEWIJS IJ; SISTERMANS EA; ROPERS HH; MARIMAN ECM
      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
    49. HOYNG CB; POPPELAARS F; VANDEPOL TJR; KREMER H; PINCKERS AJLG; DEUTMAN AF; CREMERS FPM
      GENETIC FINE MAPPING OF THE GENE FOR RECESSIVE STARGARDT DISEASE

      Human genetics
    50. HAMEL BCJ; SMEETS DFCM; SMITS APT; VANDENHELM B; KREMER H; KNOERS N; ROPERS HH; MARIMAN EC
      X-LINKED MENTAL-RETARDATION - RESULTS OF A COMBINED CLINICAL, CYTOGENETIC AND MOLECULAR APPROACH

      American journal of medical genetics
    51. HAMEL BCJ; SMEETS DFCM; SMITS APT; VANDENHELM B; KREMER H; KNOERS N; ROPER HH; MARIMAN EC
      X-LINKED MENTAL-RETARDATION - THE NIJMEGEN EXPERIENCE - HIGHLIGHTS AND PITFALLS

      American journal of medical genetics
    52. HAMEL BCJ; KREMER H; WESBYVANSWAAY E; VANDENHELM B; SMITS APT; OOSTRA BA; ROPERS HH; MARIMAN ECM
      A GENE FOR NONSPECIFIC X-LINKED MENTAL-RETARDATION (MRX41) IS LOCATEDIN THE DISTAL SEGMENT OF XQ28

      American journal of medical genetics
    53. TOLEDO SPA; BRUNNER HG; KRAAIJ R; POST M; DAHIA PLM; HAYASHIDA CY; KREMER H; THEMMEN APN
      AN INACTIVATING MUTATION OF THE LUTEINIZING-HORMONE RECEPTOR CAUSES AMENORRHEA IN A 46,XX FEMALE

      The Journal of clinical endocrinology and metabolism
    54. PEMBERTON LB; ROSS V; CUDDY P; KREMER H; FESSLER T; MCGURK E
      NO DIFFERENCE IN CATHETER SEPSIS BETWEEN STANDARD AND ANTISEPTIC CENTRAL VENOUS CATHETERS

      Archives of surgery
    55. KREMER H; KRAAIJ R; TOLEDO SPA; POST M; FRIDMAN JB; HAYASHIDA CY; VANREEN M; MILGROM E; ROPERS HH; MARIMAN E; THEMMEN APN; BRUNNER HG
      MALE PSEUDOHERMAPHRODITISM DUE TO A HOMOZYGOUS MISSENSE MUTATION OF THE LUTEINIZING-HORMONE RECEPTOR GENE

      Nature genetics
    56. BEIERHELLWIG K; KREMER H; BONN B; LINDER D; BADER H; BEIER HM
      PARTIAL SEQUENCING AND IDENTIFICATION OF 3 PROTEINS FROM EQUINE UTERINE SECRETION REGULATED BY PROGESTERONE

      Reproduction in domestic animals
    57. AKHMANOVA AS; BINDELS PCT; XU J; MIEDEMA K; KREMER H; HENNIG W
      STRUCTURE AND EXPRESSION OF HISTONE H3.3 GENES IN DROSOPHILA-MELANOGASTER AND DROSOPHILA-HYDEI

      Genome
    58. REINITZHUBER F; DOMELS HP; ELSTNER I; GRAU R; KREMER H; BURAU F
      A RADIATION PANEL CONSISTING OF HONEYCOMB ELEMENTS THROUGH WHICH GAS-FLOWS - A NEW ENERGY-SAVING STRUCTURAL UNIT FOR INDUSTRIAL FURNACES

      Stahl und Eisen
    59. KRAGEL PJ; FIORELLA RM; KREMER H
      TUMORAL FIBROSIS AND LACK OF CIRCUMSCRIPTION IN GRANULAR-CELL TUMOR OF THE BREAST

      Southern medical journal
    60. MELCHERS D; KREMER H; BICHAKJIAN CK; STEIJLEN PM
      MUTATION ANALYSIS IN PATIENTS WITH BULLOUS CONGENITAL ICHTHYOSIFORM ERYTHRODERMA OF BROCQ

      Journal of investigative dermatology
    61. KRAAIJ R; POST M; KREMER H; MILGROM E; EPPING W; BRUNNER HG; GROOTEGOED JA; THEMMEN APN
      A MISSENSE MUTATION IN THE 2ND TRANSMEMBRANE SEGMENT OF THE LUTEINIZING-HORMONE RECEPTOR CAUSES FAMILIAL MALE-LIMITED PRECOCIOUS PUBERTY

      The Journal of clinical endocrinology and metabolism
    62. KREMER H; PINCKERS A; VANDENHELM V; DEUTMAN AF; ROPERS HH; MARIMAN ECM
      LOCALIZATION OF THE GENE FOR DOMINANT CYSTOID MACULAR DYSTROPHY ON CHROMOSOME 7P

      Human molecular genetics
    63. KREMER H; MARIMAN E; OTTEN BJ; MOLL GW; STOELINGA GBA; WIT JM; JANSEN M; DROP SL; FAAS B; ROPERS SH; BRUNNER HG
      COSEGREGATION OF MISSENSE MUTATIONS OF THE LUTEINIZING-HORMONE RECEPTOR GENE WITH FAMILIAL MALE-LIMITED PRECOCIOUS PUBERTY (VOL 2, PG 1779,1993)

      Human molecular genetics
    64. KREMER H; KOCH L; ADLOFF B; BASCHEK B; SCHNEIDER O; FISCHER W
      RESULTS FROM A PILOT-STUDY ON SIGHTINGS OF HARBOR PORPOISES, PHOCOENA-PHOCOENA, AT THE NORTH-SEA COAST OF SCHLESWIG-HOLSTEIN, FRG

      Archive of fishery and marine research
    65. SMITS A; MARIMAN E; VANDENHELM B; KNOERSVANSLOBBE N; SMEETS D; KREMER H; VANDERMAAREL S; HAMEL B; ROPERS HH
      NONSPECIFIC X-LINKED MENTAL-RETARDATION - IDENTIFICATION OF SEPARATE SUBTYPES BY LINKAGE STUDIES AND DETAILED CLINICAL INVESTIGATION

      Cytogenetics and cell genetics
    66. STEIJLEN PM; KREMER H; VAKILZADEH F; HAPPLE R; LAVRIJSEN APM; ROPERS HH; MARIMAN ECM
      GENETIC-LINKAGE OF THE KERATIN TYPE-II GENE-CLUSTER WITH ICHTHYOSIS BULLOSA OF SIEMENS AND WITH AUTOSOMAL-DOMINANT ICHTHYOSIS EXFOLIATIVA

      Journal of investigative dermatology
    67. KREMER H; ZEEUWEN P; MCLEAN WHI; MARIMAN ECM; LANE EB; VANDEKERKHOF PCM; ROPERS HH; STEIJLEN PM
      ICHTHYOSIS BULLOSA OF SIEMENS IS CAUSED BY MUTATIONS IN THE KERATIN 2E GENE

      Journal of investigative dermatology
    68. KREMER H; ZEEUWEN P; MCLEAN WHI; MARIMAN ECM; LANE EB; VANDEKERKHOF PCM; ROPERS HH; STEIJLEN PM
      ICHTHYOSIS BULLOSA OF SIEMENS IS CAUSED BY MUTATIONS IN THE KERATIN 2E GENE

      Journal of investigative dermatology
    69. KREMER H; MARIMAN E; OTTEN BJ; MOLL GW; STOELINGA GBA; WIT JM; JANSEN M; DROP SL; FAAS B; ROPERS HH; BRUNNER HG
      COSEGREGATION OF MISSENSE MUTATIONS OF THE LUTEINIZING-HORMONE RECEPTOR GENE WITH FAMILIAL MALE-LIMITED PRECOCIOUS PUBERTY

      Human molecular genetics
    70. KREMER H
      ECHO-POOR EPIGASTRIC MASS - GIANT LEIOMYOMA OF THE STOMACH

      Leber, Magen, Darm
    71. PINCKERS A; CRUYSBERG JRM; KREMER H; AANDEKERK AL
      ACETAZOLAMIDE IN DOMINANT CYSTOID MACULAR DYSTROPHY - A PILOT-STUDY

      Ophthalmic paediatrics and genetics
    72. KUMMELL HC; VANLEEUWEN P; HECKMANN C; ENGELKE P; KESTING G; KREMER H; BECHER A
      QUALITY-OF-LIFE AND CIRCADIAN VARIATION OF HEART-RATE AND HEART-RATE-VARIABILITY IN SHORT-TERM SURVIVORS AND NONSURVIVORS AFTER ACUTE MYOCARDIAL-INFARCTION

      Clinical cardiology
    73. RAO NS; KREMER H
      UNIVERSAL METHOD FOR CALCULATION OF INJECTOR MIXERS

      Chemieingenieurtechnik
    74. KREMER H; VANDENHELM B; SMITS APT; HAMEL BCJ; ARTS WF; WESBYVANSWAAY E; OOSTRA BA; VANDERMAAREL SM; MARIMAN ECM; ROPERS HH
      LOCALIZATION OF GENES FOR NONSPECIFIC AND SYNDROMAL X-LINKED MENTAL-RETARDATION

      American journal of human genetics
    75. KREMER H; ROSS M
      THORACIC ACTINOMYCOSIS MASKING AS A CENTR AL BRONCHIAL-CARCINOMA

      Deutsche Medizinische Wochenschrift
    76. Kremer, G. H.
      Tax effects in the dutch bond market

      Rivista di matematica per le scienze economiche e sociali sociali


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 31/05/20 alle ore 07:06:35