Catalogo Articoli (Spogli Riviste)

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La ricerca find articoli where authors phrase all words ' Dundar, M' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 22 riferimenti
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    1. Dundar, M; Kurtoglu, S; Elmas, B; Demiryilmaz, F; Candemir, Z; Ozkul, Y; Durak, AC
      A case with adducted thumb and club foot syndrome

      CLINICAL DYSMORPHOLOGY
    2. Dundar, M; Lowther, G; Colgan, J; Ozkul, Y; Candemir, Z; Saatci, C; Kurtoglu, S; Watt, J; Morrison, N
      A case with Waardenburg syndrome presenting with two separate translocations - one reciprocal and one complex

      CLINICAL DYSMORPHOLOGY
    3. Dundar, SO; Dundar, M; Kocak, I; Dayanir, Y; Ozkan, SB
      Effect of sildenafil on ocular haemodynamics

      EYE
    4. Dundar, M; Kocak, I; Erkus, M; Celasun, B
      The effect of estrogen-replacement therapy on clitoral-cavernosal tissue in oophorectomized rats: A histo-quantitative study by image analyzer

      UROLOGICAL RESEARCH
    5. Dundar, M; Kocak, I; Culhaci, N
      A new experimental model for cryptorchidism: inguinoscrotal approach

      UROLOGICAL RESEARCH
    6. Dundar, M; Erol, H; Kocak, I; Kacar, F
      Liposarcoma of the spermatic cord

      UROLOGIA INTERNATIONALIS
    7. Dundar, M; Gordon, TM; Ozyazgan, I; Oguzkaya, F; Ozkul, Y; Cooke, A; Wilkinson, AG; Holloway, S; Goodman, FR; Tolmie, JL
      A novel acropectoral syndrome maps to chromosome 7q36

      JOURNAL OF MEDICAL GENETICS
    8. Dundar, M; Lowther, G; Acar, H; Kurtoglu, S; Demiryilmaz, F; Kucukaydin, M
      A case of ambiguous genitalia presenting with a 45,X/46,Xr(Y)(p11.2;q11.23)/47,X,idic(Y)(p11.2),idic(Y)(p11.2) karyotype

      ANNALES DE GENETIQUE
    9. Kurtoglu, S; Dundar, M; Kumandas, S; Gunduz, Z; Uzum, K; Durak, AC; Caksen, H
      Patient with Weismann-Netter and Stuhl (toxopachyosteosis) syndrome with communicant hydrocephalus and arachnoid cyst

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    10. Dundar, M; Inal, OT; Stringer, J
      The effect of particle size on the erosion of a ductile material at the low particle size limit (vol 233, pg 727, 1999)

      WEAR
    11. Dundar, M; Keles, O; Inal, OT
      Deformation created by the impact of small angular and spherical particleson individual grains

      JOURNAL OF MATERIALS SCIENCE
    12. Turan, MT; Esel, E; Dundar, M; Candemir, Z; Basturk, M; Sofuoglu, S; Ozkul, Y
      Female-to-male transsexual with 47,XXX karyotype

      BIOLOGICAL PSYCHIATRY
    13. Dundar, M; Inal, OT; Stringer, J
      The effect of particle size on the erosion of a ductile material at the low particle size limit

      WEAR
    14. Dundar, M; Inal, OT
      Solid particle erosion of alpha-brass with 5 and 25 mu m particles at normal incidence

      WEAR
    15. CEYLANER G; CEYLANER S; DUNDAR M
      A FAMILY WITH OSTEOGENESIS IMPERFECTA, FRONTONASAL DYSPLASIA, EAR ABNORMALITY AND MENTAL-RETARDATION

      Journal of Medical Genetics
    16. DUNDAR M; CEYLANER S; CEYLANER G
      A CASE WITH MULTIPLE PTERGIUM SYNDROME (ESCOBAR-SYNDROME)

      Journal of Medical Genetics
    17. KURTOGLU S; DUNDAR M; HALLAC IK; UZUM K; OKUMUS Y; OKTEM T
      POLYCYSTIC KIDNEY-DISEASE, BILIARY DYSGENESIS IN A PATIENT WITH LARSENS-SYNDROME

      Clinical genetics
    18. DUNDAR M; DEMIRYILMAZ F; DEMIRYILMAZ I; KUMANDAS S; ERKILIC K; KENDIRCI M; TUNCEL M; OZYAZGAN I; TOLMIE JL
      AN AUTOSOMAL RECESSIVE ADDUCTED THUMB CLUB FOOT SYNDROME OBSERVED IN TURKISH COUSINS

      Clinical genetics
    19. DUNDAR M; ERKILIC K; DEMIRYILMAZ F; KUCUKAYDIN M; KENDIRCI M; OKUR H; KAZEZ A
      CONGENITAL ALACRIMA IN A PATIENT WITH G-(OPITZ-FRIAS)-SYNDROME

      Human genetics
    20. DUNDAR M; LANYON WG; CONNOR JM
      DETECTION OF GERMLINE MUTATIONS IN THE RB1 GENE USING AMPLIFICATION MISMATCH DETECTION (AMD) ANALYSIS AND DIRECT SEQUENCING OF PCR PRODUCTS

      Journal of Medical Genetics
    21. DUNDAR M; LANYON WG; CONNOR JM
      MOLECULAR PATHOLOGY OF THE RB1 GENE IN RETINOBLASTOMA, BREAST AND BLADDER-TUMORS

      Journal of Medical Genetics
    22. DUNDAR M; LANYON WG; CONNOR JM
      SCOTTISH FREQUENCY OF THE COMMON G985 MUTATION IN THE MEDIUM-CHAIN ACYL-COA DEHYDROGENASE (MCAD) GENE AND THE ROLE OF MCAD DEFICIENCY IN SUDDEN-INFANT-DEATH-SYNDROME (SIDS)

      Journal of inherited metabolic disease


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 30/05/20 alle ore 02:22:44