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La ricerca find articoli where authors phrase all words 'Froster, UG' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 34 riferimenti
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    1. Kinne, RW; Liehr, T; Beensen, V; Kunisch, E; Zimmermann, T; Holland, H; Pfeiffer, R; Stahl, HD; Lungershausen, W; Hein, G; Roth, A; Emmrich, F; Claussen, U; Froster, UG
      Mosaic chromosomal aberrations in synovial fibroblasts of patients with rheumatoid arthritis, osteoarthritis, and other inflammatory joint diseases

      ARTHRITIS RESEARCH
    2. Faber, R; Stepan, H; Schilde, M; Froster, UG; Horn, LC
      Accuracy of prenatal sonography in terminated pregnancies - a retrospective analysis of results and parameters of influence

      ZEITSCHRIFT FUR GEBURTSHILFE UND NEONATOLOGIE
    3. Kotzot, D; Holland, H; Keller, E; Froster, UG
      Maternal isochromosome 7q and paternal isochromosome 7p in a boy with growth retardation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    4. Rueffert, H; Olthoff, D; Deutrich, C; Froster, UG
      Determination of a positive malignant hyperthermia (MH) disposition without the in vitro contracture test in families carrying the RYR1 Arg614Cys mutation

      CLINICAL GENETICS
    5. Rueffert, H; Olthoff, D; Deutrich, C; Thamm, B; Froster, UG
      Homozygous and heterozygous Arg614Cys mutations (1840C -> T) in the ryanodine receptor gene co-segregate with malignant hyperthermia susceptibility in a German family

      BRITISH JOURNAL OF ANAESTHESIA
    6. Kotzot, D; Holland, H; Kohler, M; Froster, UG
      A complex chromosome rearrangement involving chromosome 8, 11, and 12 analyzed by conventional cytogenetic investigations, fluorescence in situ hybridisation, and spectral karyotyping

      ANNALES DE GENETIQUE
    7. Froster, UG; Horn, LC; Holland, H; Strenge, S; Faber, R
      Prenatal diagnosis of del(15)(q26.1) and del(18)(q21.3) due to an unbalanced de novo translocation: ultrasound, molecular cytogenetic and autopsy findings

      PRENATAL DIAGNOSIS
    8. Froster, UG; Reichenbach, H
      Trisomy of 5p and marker chromosomes

      AMERICAN JOURNAL OF MEDICAL GENETICS
    9. Meiner, A; Faber, R; Horn, LC; Reichenbach, H; Froster, UG
      Prenatal detection of a giant bilateral thoracic vascular lesion: Prognostic evaluation and genetic aspects

      PRENATAL DIAGNOSIS
    10. Vondran, S; Edelmann, J; Holland, H; Wolf, C; Strenge, S; Thamm, B; Thiele, H; Froster, UG
      Pitfalls in prenatal diagnosis of DMD due to placental mosaicism of the X-chromosomes: Prenatal and postnatal findings in a fetus with a deletion of exons 67-71 of the dystrophin gene

      PRENATAL DIAGNOSIS
    11. Reichenbach, H; Holland, H; Dalitz, E; Demandt, C; Meiner, A; Chudoba, I; Lemke, J; Claussen, U; Froster, UG
      De novo complete trisomy 5p: Clinical report and FISH studies

      AMERICAN JOURNAL OF MEDICAL GENETICS
    12. MEINER A; HOLLAND H; REICHENBACH H; HORN LC; FABER R; FROSTER UG
      TETRAPLOIDY IN A GROWTH-RETARDED FETUS WITH A THICK PLACENTA

      Prenatal diagnosis
    13. FROSTER UG; JACKSON L
      (MIS)CLASSIFYING LIMB DEFICIENCIES - REPLY TO ACADEMICIANS ARE MORE LIKELY TO SHARE EACH OTHERS TOOTHBRUSH THAN EACH OTHERS NOMENCLATURE (COHEN, 1982) - REPLY

      American journal of medical genetics
    14. Strenge, S; Froster, UG
      Microcephaly-lymphedema syndrome: Report of a family with short stature asadditional manifestation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    15. FROSTER UG; STALLMACH T; WISSER J; HEBISCH G; ROBBIANI MB; HUCH R; HUCH A
      LETHAL MULTIPLE PTERYGIUM SYNDROME - SUGGESTION FOR A CONSISTENT PATHOLOGICAL WORK-UP AND REVIEW OF REPORTED CASES

      American journal of medical genetics
    16. THAMM B; STRENGE S; REICHENBACH H; WAND D; FROSTER UG
      ANALYSIS OF CYSTIC-FIBROSIS TRANSMEMBRANE REGULATOR (CFTR) GENE-MUTATIONS IN MEN WITH CONGENITAL AGENESIS OF VAS-DEFERENS

      Fertility and sterility
    17. FROSTER UG; BRINER J; ZIMMERMANN R; HUCH R; HUCH A
      BILATERAL BRACHIAL AMELIA, FACIAL CLEFTS, ENCEPHALOCELE, ORBITAL CYSTAND OMPHALOCELE - A RECURRENT FETAL MALFORMATION PATTERN COMING INTO FOCUS

      Clinical dysmorphology
    18. FROSTER UG
      ACADEMICIANS ARE MORE LIKELY TO SHARE EACH OTHERS TOOTHBRUSH THAN EACH OTHERS NOMENCLATURE [COHEN, 1982]

      American journal of medical genetics
    19. FROSTER UG; WALLNER SJ; REUSCHE E; SCHWINGER E; REHDER H
      VACTERL WITH HYDROCEPHALUS AND BRANCHIAL ARCH DEFECTS - PRENATAL, CLINICAL, AND AUTOPSY FINDINGS IN 2 BROTHERS

      American journal of medical genetics
    20. FROSTER UG; KOLDITZ P; WISSER J; ROBBIANI RB; STALLMACH T; HEBISCH G; HUCH R; HUCH A
      DIAPHRAGMATIC DEFECTS, LIMB DEFICIENCIES, AND OSSIFICATION DEFECTS OFTHE SKULL - A DISTINCTIVE MALFORMATION SYNDROME

      American journal of medical genetics
    21. FROSTER UG; JACKSON L
      LIMB DEFECTS AND CHORIONIC VILLUS SAMPLING - REPLY

      Lancet
    22. FROSTER UG; JACKSON L
      LIMB DEFECTS AND CHORIONIC VILLUS SAMPLING - RESULTS FROM AN INTERNATIONAL REGISTRY, 1992-94

      Lancet
    23. FROSTER UG; ZIMMERMANN R; WISSER J
      LIMB DEFECTS AFTER CHORIONIC VILLUS SAMPLING

      Obstetrics and gynecology
    24. FROSTER UG
      GENETIC RISKS OF IN-VITRO-FERTILIZATION - A REVIEW

      Geburtshilfe und Frauenheilkunde
    25. MESCHEDE D; FROSTER UG; BERGMANN M; NIESCHLAG E
      FAMILIAL PERICENTRIC-INVERSION OF CHROMOSOME-1 (P34Q23) AND MALE-INFERTILITY WITH STAGE-SPECIFIC SPERMATOGENIC ARREST

      Journal of Medical Genetics
    26. FROSTER UG; JACKSON L
      SAFETY OF CHORIONIC VILLUS SAMPLING - RESULTS FROM AN INTERNATIONAL REGISTRY

      American journal of human genetics
    27. FROSTER UG
      MODERN GENETICS - INTRODUCTION

      Archives of gynecology and obstetrics
    28. FROSTER UG; LETTAU R; OBERHEUSER F
      LIMB ABNORMALITIES FOLLOWING CHORIONIC VI LLUS SAMPLING AMONG SOME PATIENTS AT THE GYNECOLOGICAL CLINIC OF THE MEDICAL-UNIVERSITY-OF-LUBECK

      Archives of gynecology and obstetrics
    29. FROSTER UG; REHDER H; HOHN W; OBERHEUSER F
      CRANIOFACIAL ANOMALIES, ABNORMAL HAIR, CAMPTODACTYLY, AND CAUDAL APPENDAGE (TEEBI-SHALTOUT SYNDROME) - CLINICAL AND AUTOPSY FINDINGS

      American journal of medical genetics
    30. MESCHEDE D; FROSTER UG; GULLOTTA F; NIESCHLAG E
      REPRODUCTIVE FAILURE IN A PATIENT WITH NEUROFIBROMATOSIS-NOONAN SYNDROME

      American journal of medical genetics
    31. FROSTER UG; GORTNER L
      THROMBOCYTOPENIA IN THE BRACHMANN-DE-LANGE SYNDROME

      American journal of medical genetics
    32. FROSTER UG; BAIRD PA
      CONGENITAL-DEFECTS OF THE LIMBS IN STILLBIRTHS - DATA FROM A POPULATION-BASED STUDY

      American journal of medical genetics
    33. FROSTER UG; BAIRD PA
      AMNIOTIC BAND SEQUENCE AND LIMB DEFECTS - DATA FROM A POPULATION-BASED STUDY

      American journal of medical genetics
    34. FROSTER UG; BAIRD PA
      MATERNAL FACTORS, MEDICATIONS, AND DRUG EXPOSURE IN CONGENITAL LIMB REDUCTION DEFECTS

      Environmental health perspectives


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/10/20 alle ore 03:33:27