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La ricerca find articoli where soggetti phrase all words 'NORMAL INTELLIGENCE' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 30 riferimenti
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    1. Robinson, WP; Beever, C; Brown, CJ; Stephenson, MD
      Skewed X inactivation and recurrent spontaneous abortion

      SEMINARS IN REPRODUCTIVE MEDICINE
    2. Baron-Cohen, S; Wheelwright, S; Skinner, R; Martin, J; Clubley, E
      The Autism-Spectrum Quotient (AQ): Evidence from Asperger syndrome/high-functioning autism, males and females, scientists and mathematicians

      JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
    3. Sutcliffe, MJ; Mueller, OT; Kousseff, BG; Dumont, DP; McFarland, JA; Mawani, F; Conforto, D; Ranells, JD
      Three cell line mosaicism involving structural and numerical abnormalitiesof chromosome 18 in a 3.5-year-old girl: 47,XX,+18/47,XX,+del(18)(q22)/46,XX

      AMERICAN JOURNAL OF MEDICAL GENETICS
    4. Robinson, WP; McFadden, DE; Stephenson, MD
      The origin of abnormalities in recurrent aneuploidy/polyploidy

      AMERICAN JOURNAL OF HUMAN GENETICS
    5. Ward, KJ
      Genetic factors in recurrent pregnancy loss

      SEMINARS IN REPRODUCTIVE MEDICINE
    6. Abdel-Salam, G; Czeizel, AE
      The second unrelated case with isolated microcephaly and normal intelligence (Microcephalia vera)

      CLINICAL DYSMORPHOLOGY
    7. Alessandri, JL; Graber, D; Tiran-Rajaofera, I; Montbrun, A; Pilorget, H; Samperiz, S; Attali, T; de Napoli-Cocci, S
      Feingold syndrome (MODED syndrome: Microcephaly-oculo-digito-esophageal-duodenal syndrome).

      ARCHIVES DE PEDIATRIE
    8. Piersall, LD; Dowton, SB; McAlister, WH; Waggoner, DJ
      Vertebral anomalies in a new family with ODED syndrome

      CLINICAL GENETICS
    9. Celli, J; van Beusekom, E; Hennekam, RCM; Gallardo, ME; Smeets, DFCM; de Cordoba, SR; Innis, JW; Frydman, M; Konig, R; Kingston, H; Tolmie, J; Govaerts, LCP; van Bokhoven, H; Brunner, HG
      Familial syndromic esophageal atresia maps to 2p23-p24

      AMERICAN JOURNAL OF HUMAN GENETICS
    10. Moynihan, L; Jackson, AP; Roberts, E; Karbani, G; Lewis, I; Corry, P; Turner, G; Mueller, RF; Lench, NJ; Woods, CG
      A third novel locus for primary autosomal recessive microcephaly maps to chromosome 9q34

      AMERICAN JOURNAL OF HUMAN GENETICS
    11. Peschka, B; Leygraaf, J; van der Ven, K; Montag, M; Schartmann, B; Schubert, R; van der Ven, H; Schwanitz, G
      Type and frequency of chromosome aberrations in 781 couples undergoing intracytoplasmic sperm injection

      HUMAN REPRODUCTION
    12. Digweed, M; Reis, A; Sperling, K
      Nijmegen Breakage Syndrome: consequences of defective DNA double strand break repair

      BIOESSAYS
    13. Sangha, KK; Stephenson, MD; Brown, CJ; Robinson, WP
      Extremely skewed X-chromosome inactivation is increased in women with recurrent spontaneous abortion

      AMERICAN JOURNAL OF HUMAN GENETICS
    14. PREVEL CD; EPPLEY BL; MCCARTY M
      ACROCEPHALOSYNDACTYLY SYNDROMES - A REVIEW

      The Journal of craniofacial surgery
    15. KUMAR D; DUGGAN MB; MUELLER RF; KARBANI G
      FAMILIAL APLASIA HYPOPLASIA OF PELVIS, FEMUR, FIBULA, AND ULNA WITH ABNORMAL DIGITS IN AN INBRED PAKISTANI MUSLIM FAMILY - A POSSIBLE NEW AUTOSOMAL RECESSIVE DISORDER WITH OVERLAPPING MANIFESTATIONS OF THE SYNDROMES OF FUHRMANN, AL-AWADI, AND RAAS-ROTHSCHILD

      American journal of medical genetics
    16. PLESSIS G; LETREUST M; LEMAIRE F; MAUGARD T; CAU D
      TRISOMY-18 MOSAICISM IN A MILDLY RETARDED BOY WITH POSTNATAL OVERGROWTH

      Annales de genetique
    17. SAAR K; CHRZANOWSKA KH; STUMM M; JUNG M; NURNBERG G; WIENKER TF; SEEMANOVA E; WEGNER RD; REIS A; SPERLING K
      THE GENE FOR THE ATAXIA-TELANGIECTASIA VARIANT, NIJMEGEN BREAKAGE SYNDROME, MAPS TO A 1-CM INTERVAL ON CHROMOSOME 8Q21

      American journal of human genetics
    18. GREALLY JM; NEISWANGER K; CUMMINS JH; BOONE LY; LENKEY SG; WENGER SL; LEWIS JL; FISCHER D; PAUL RA; STEELE MW
      A MOLECULAR ANATOMICAL ANALYSIS OF MOSAIC TRISOMY-16

      Human genetics
    19. FRANCESCHINI P; GUALA A; CAMERANO P; FRANCESCHINI D; VARDEU MP; SIGNORILE F
      ULLRICH-TURNER PHENOTYPE WITH UNUSUAL MANIFESTATION IN A PATIENT WITHMOSAICISM 45,X 47,XX,+18/

      American journal of medical genetics
    20. SATGE D; GENEIX A; GOBURDHUN J; LASNEDESMET P; ROSENTHAL C; ARNAUD R; MALET P
      A HISTORY OF MISCARRIAGES AND MILD PROGNATHISM AS POSSIBLE MODE OF PRESENTATION OF MOSAIC TRISOMY-18 IN WOMEN

      Clinical genetics
    21. PILLAR G; ZAAROOR M; GERSHONIBARUCH R
      AUTOSOMAL-DOMINANT HOLOCALVARIAL CRANIOSYNOSTOSIS

      Child's nervous system
    22. LEYTEN QH; GABREELS FJM; RENIER WO; VANENGELEN BGM; TERLAAK HJ; SENGERS RCA; THIJSSEN HOM
      WHITE-MATTER ABNORMALITIES IN CONGENITAL MUSCULAR-DYSTROPHY

      Journal of the neurological sciences
    23. GREEN AJ; YATES JRW; TAYLOR AMR; BIGGS P; MCGUIRE GM; MCCONVILLE CM; BILLING CJ; BARNES ND
      SEVERE MICROCEPHALY WITH NORMAL INTELLECTUAL-DEVELOPMENT - THE NIJMEGEN-BREAKAGE-SYNDROME

      Archives of Disease in Childhood
    24. DLUZNIEWSKA A; TREDOWSKASKOCZEN D; ARMATA J; TACIK J
      MICROCEPHALY AND CHILDHOOD NON-HODGKINS-LYMPHOMA

      Archives of Disease in Childhood
    25. BUNDEY S
      CLINICAL AND GENETIC FEATURES OF ATAXIA-TELANGIECTASIA

      International journal of radiation biology
    26. NEVIN NC; SILVESTRI J; KERNOHAN DC; HUTCHINSON WM
      ORAL-FACIAL-DIGITAL SYNDROME WITH RETINAL ABNORMALITIES - OFDS TYPE-IX - A FURTHER CASE-REPORT

      American journal of medical genetics
    27. TEEBI AS
      AUTOSOMAL RECESSIVE DISORDERS AMONG ARABS - AN OVERVIEW FROM KUWAIT

      Journal of Medical Genetics
    28. MOESCHLER JB; GRAHAM JM
      MILD BRACHMANN-DELANGE SYNDROME - PHENOTYPIC AND DEVELOPMENTAL CHARACTERISTICS OF MILDLY AFFECTED INDIVIDUALS

      American journal of medical genetics
    29. SAAL HM; SAMANGOSPROUSE CA; RODNAN LA; ROSENBAUM KN; CUSTER DA
      BRACHMANN-DELANGE SYNDROME WITH NORMAL IQ

      American journal of medical genetics
    30. JENDERNY J; CALIEBE A; BEYER C; GROTE W
      TRANSMISSION OF A RING CHROMOSOME-18 FROM A MOTHER WITH 46,XX 47,XX,+R(18) MOSAICISM TO HER DAUGHTER, RESULTING IN A 46,XX,R(18) KARYOTYPE/

      Journal of Medical Genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 24/01/21 alle ore 01:49:39