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La ricerca find articoli where authors phrase all words ' Midro, AT' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 14 riferimenti
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    1. Dorr, S; Midro, AT; Farber, C; Giannakudis, J; Hansmann, I
      Construction of a detailed physical and transcript map of the candidate region for Russell-Silver syndrome on chromosome 17q23-q24

      GENOMICS
    2. Ludecke, HJ; Schaper, J; Meinecke, P; Momeni, P; Gross, S; von Holtum, D; Hirche, H; Abramowicz, MJ; Albrecht, B; Apacik, C; Christen, HJ; Claussen, U; Devriendt, K; Fastnacht, E; Forderer, A; Friedrich, U; Goodship, THJ; Greiwe, M; Hamm, H; Hennekam, RCM; Hinkel, GK; Hoeltzenbein, M; Kayserili, H; Majewski, F; Mathieu, M; McLeod, R; Midro, AT; Moog, U; Nagai, T; Niikawa, N; Orstavik, KH; Plochl, E; Seitz, C; Schmidtke, J; Tranebjaerg, L; Tsukahara, M; Wittwer, B; Zabel, B; Gillessen-Kaesbach, G; Horsthemke, B
      Genotypic and phenotypic spectrum in tricho-rhino-phalangeal syndrome types I and III

      AMERICAN JOURNAL OF HUMAN GENETICS
    3. Midro, AT; Panasiuk, B; Stasiewicz-Jarocka, B; Iwanowski, PS; Fauth, C; Speicher, MR; Lesniewicz, R
      Risk estimates for carriers of chromosome reciprocal translocation t(4;9)(p15.2;p13)

      CLINICAL GENETICS
    4. Hiel, JA; Weemaes, CM; van den Heuvel, LP; van Engelen, BG; Gabreels, FJ; Smeets, DF; van der Burgt, I; Chrzanovska, KH; Bernatowska, E; Krajewska-Walasek, M; Bialecka, M; Abramczuk, D; Gregorek, H; Michalkiewicz, I; Perek, D; Midro, AT; Seemanova, E; Belohradsky, BH; Solder, B; Barbi, G; Wegner, RD; Sperling, K; Dixon, J; Maraschio, P; Marseglia, GL; Green, A; Taylor, AM; Der Kaloustian, VM; Komatsu, K; Matsuura, S; Conley, ME; Concannon, P; Gatti, RA
      Nijmegen breakage syndrome

      ARCHIVES OF DISEASE IN CHILDHOOD
    5. Kraakman-van der Zwet, M; Overkamp, WJI; Friedl, AA; Klein, B; Verhaegh, GWCT; Jaspers, NGJ; Midro, AT; Eckardt-Schupp, F; Lohman, PHM; Zdzienicka, MZ
      Immortalization and characterization of Nijmegen Breakage Syndrome fibroblasts

      MUTATION RESEARCH-DNA REPAIR
    6. SCHERER G; HELD M; ERDEL M; MESCHEDE D; HORST J; LESNIEWICZ R; MIDRO AT
      3 NOVEL SRY MUTATIONS IN XY GONADAL-DYSGENESIS AND THE ENIGMA OF XY GONADAL-DYSGENESIS CASES WITHOUT SRY MUTATIONS

      Cytogenetics and cell genetics
    7. Hassmann, E; Skotnicka, B; Midro, AT; Musiatowicz, M
      Distortion products otoacoustic emissions in diagnosis of hearing loss in Down syndrome

      INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY
    8. MIDRO AT; PANASIUK B; ZADROZNATOLWINSKA B
      EARLIER APPEARANCE OF SUBBAND XP21.2 ON THE LATE REPLICATION CHROMOSOME-X IN RETT-SYNDROME GIRL

      European child & adolescent psychiatry
    9. PANASIUK B; MIDRO AT; LESNIEWICZ R; KRAJEWSKAWALASEK M; CHMIELINSKA E; LIEBAERS I; VANASSCHE E; WOLCZYNSKI S
      DISTINCT CLINICAL EFFECT IN SIMILAR RECIPROCAL X-8 TRANSLOCATIONS CARRIERS

      Cytogenetics and cell genetics
    10. PANASIUK B; MIDRO AT; ZADROZNATOLWINSKA B
      EARLIER FINISHING OF XP21.2 SUBBAND REPLICATION OF THE INACTIVE X-CHROMOSOME IN RETT-SYNDROME GIRL BUT NOT IN HER 47,XXX MOTHER

      Clinical genetics
    11. MIDRO AT; OLCHOWIK B; ROGOWSKA M; HUBERT E; HASSMANPOZNANSKA E; PAPASZ A; SZULC S; WISNIEWSKI A
      FLOATING-HARBOR-SYNDROME - CASE-REPORT AND FURTHER SYNDROME DELINEATION

      Annales de genetique
    12. DOERR S; FAERBER C; MIDRO AT; LEPASLIER D; GIANNAKUDIS J; HANSMANN I
      POSITIONAL CLONING OF THE LOCUS FOR RUSSELL-SILVER-SYNDROME (RSS) ON CHROMOSOME

      American journal of human genetics
    13. MIDRO AT; DEBEK K; SAWICKA A; MARCINKIEWICZ D; ROGOWSKA M
      2ND OBSERVATION OF SILVER-RUSSEL SYNDROME IN A CARRIER OF A RECIPROCAL TRANSLOCATION WITH ONE BREAKPOINT AT SITE-17Q25

      Clinical genetics
    14. MIDRO AT; STENGELRUTKOWSKI S; STENE J
      EXPERIENCES WITH RISK ESTIMATES FOR CARRIERS OF CHROMOSOMAL RECIPROCAL TRANSLOCATIONS

      Clinical genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 27/01/21 alle ore 22:29:17