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La ricerca find articoli where soggetti phrase all words 'Potter sequence' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 12 riferimenti
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    1. Strauss, A; Hasbargen, U; Paek, B; Fuchshuber, S; Hepp, H
      Prenatal diagnosis of renal dysplasia

      ZEITSCHRIFT FUR GEBURTSHILFE UND NEONATOLOGIE
    2. Chrobok, V; Simakova, E; Liang, JN
      Residual mesenchyme in the middle ear cavity of the newborn with malformation of the kidney

      CLINICAL OTOLARYNGOLOGY
    3. 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
    4. DEVRIENDT K; MOERMAN P; VANSCHOUBROECK D; VANDENBERGHE K; FRYNS JP
      CHROMOSOME 22Q11 DELETION PRESENTING AS THE POTTER SEQUENCE

      Journal of Medical Genetics
    5. ZLOTOGORA J; ARIEL I; ORNOY A; YAGEL S; EIDELMAN AI
      THOMAS SYNDROME - POTTER SEQUENCE WITH CLEFT-LIP PALATE AND CARDIAC ANOMALIES

      American journal of medical genetics
    6. RUDNIKSCHONEBORN S; SCHULER HM; SCHWANITZ G; HANSMANN M; ZERRES K
      FURTHER ARGUMENTS FOR NON-FORTUITOUS ASSOCIATION OF POTTER SEQUENCE WITH XYY MALES

      Annales de genetique
    7. ARIEL I; WELLS TR; LANDING BH; SAGI M; BAROZ B; RON N; ROSENMANN E
      FAMILIAL RENAL TUBULAR DYSGENESIS - A DISORDER NOT ISOLATED TO PROXIMAL CONVOLUTED TUBULES

      PEDIATRIC PATHOLOGY & LABORATORY MEDICINE
    8. ORTMANN M; QUERFELD U; STOLLORZ M; SCHRODER R
      RENAL TUBULAR DYSGENESIS ASSOCIATED WITH RENAL-VEIN THROMBOSIS

      Der Pathologe
    9. VANBUGGENHOUT GJM; VERBRUGGEN J; FRYNS JP
      RENAL AGENESIS AND TRISOMY-22 - CASE-REPORT AND REVIEW

      Annales de genetique
    10. SCARCELLA A; PECORARO C; DAGNELLO MR; SOLE AN
      RENAL TUBULAR DYSGENESIS WITHOUT PULMONARY HYPOPLASIA

      Pediatric nephrology
    11. FISCHLER BR; BERG UB
      POTTER SEQUENCE AND CONSANGUINITY - A CASE-REPORT

      Pediatric nephrology
    12. KADHIM HJ; LAMMENS M; GOSSEYE S; GADISSEUX JF; EVRARD P
      BRAIN DEFECTS IN INFANTS WITH POTTER SYNDROME (OLIGOHYDRAMNIOS SEQUENCE)

      Pediatric pathology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/10/20 alle ore 03:09:15