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La ricerca find articoli where authors phrase all words ' Moeschler, JB' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 16 riferimenti
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    1. Cunniff, C; Frias, JL; Kaye, C; Moeschler, JB; Panny, SR; Trotter, TL
      Maternal phenylketonuria

      PEDIATRICS
    2. Cunniff, C; Frias, JL; Kaye, C; Moeschler, JB; Panny, SR; Trotter, TL
      Health supervision for children with Down syndrome

      PEDIATRICS
    3. Cunniff, C; Frias, JL; Kaye, C; Moeschler, JB; Panny, SR; Trotter, TL; Hanson, JW; Williams, J; Moore, CA; Lloyd-Puryear, M; de la Cruz, F; Cho, S; Desposito, F; Hoyme, HE; Hall, L
      Molecular genetic testing in pediatric practice: A subject review

      PEDIATRICS
    4. Frias, J; Levine, LS; Oberfield, SE; Pang, S; Silverstein, J; Schwartz, RP; Hansen, IL; Kaufman, F; Varma, SK; Oberfield, SE; Silverstein, J; Levitsky, L; Suriano, MJ; Poulin, L; Cunniff, C; Frias, JL; Kaye, C; Moeschler, JB; Panny, SR; Trotter, TL; de la Cruz, F; Hanson, JW; Lloyd-Puryear, M; Moore, CA; Williams, J; Hoyme, HE; Hall, L
      Technical report: Congenital adrenal hyperplasia

      PEDIATRICS
    5. Mohandas, TK; Park, JP; Spellman, RA; Filiano, JJ; Mamourian, AC; Hawk, AB; Belloni, DR; Noll, WW; Moeschler, JB
      Paternally derived de novo interstitial duplication of proximal 15q in a patient with developmental delay

      AMERICAN JOURNAL OF MEDICAL GENETICS
    6. PARK JP; MOESCHLER JB; HANI VH; HAWK AB; BELLONI DR; NOLL WW; MOHANDAS TK
      MATERNAL DISOMY AND PRADER-WILLI-SYNDROME CONSISTENT WITH GAMETE COMPLEMENTATION IN A CASE OF FAMILIAL TRANSLOCATION (3-15) (P25-Q11.2)

      American journal of medical genetics
    7. PARK JP; MOESCHLER JB; DAVIES WS; PATEL PI; MOHANDAS TK
      SMITH-MAGENIS-SYNDROME RESULTING FROM A DE-NOVO DIRECT INSERTION OF PROXIMAL 17Q INTO 17P11.2

      American journal of medical genetics
    8. PARK JP; MOESCHLER JB
      ISOCHROMOSOME 18Q REVISITED

      Prenatal diagnosis
    9. BUTLER MG; HEDGES LK; ROGAN PK; SEIP JR; CASSIDY SB; MOESCHLER JB
      KLINEFELTER-SYNDROME AND TRISOMY-X-SYNDROME IN PATIENTS WITH PRADER-WILLI-SYNDROME AND UNIPARENTAL MATERNAL DISOMY OF CHROMOSOME-15 - A COINCIDENCE

      American journal of medical genetics
    10. WENG EY; MOESCHLER JB; GRAHAM JM
      LONGITUDINAL OBSERVATIONS ON 15 CHILDREN WITH WIEDEMANN-BECKWITH SYNDROME

      American journal of medical genetics
    11. MOESCHLER JB; FILIANO JJ; HANI V; RAWNSLEY E
      MOTHER AND DAUGHTER DEMONSTRATING FEATURES OF BOTH ANKYLOBLEPHARON FILIFORME ADNATUM AND CLEFT-PALATE (MIM-NUMBER-106250) AND HAY-WELLS SYNDROME (MIM-NUMBER-106260)

      American journal of human genetics
    12. BUTLER MG; HEDGES LK; MOESCHLER JB
      12-YEAR-OLD FEMALE WITH BOTH PRADER-WILLI AND TRISOMY-X SYNDROMES

      American journal of human genetics
    13. HANI VH; PARK J; ALLEN EF; MOESCHLER JB
      PARACENTRIC INVERSION OF CHROMOSOME-18 WITH DUPLICATION OF THE INVERTED MATERIAL IN A CHILD DUE TO A MATERNAL PARACENTRIC INVERSION OF 18Q

      American journal of human genetics
    14. MOESCHLER JB; GRAHAM JM
      MILD BRACHMANN-DELANGE SYNDROME - PHENOTYPIC AND DEVELOPMENTAL CHARACTERISTICS OF MILDLY AFFECTED INDIVIDUALS

      American journal of medical genetics
    15. BRADDOCK SR; LACHMAN RS; STOPPENHAGEN CC; CAREY JC; IRELAND M; MOESCHLER JB; CUNNIFF C; GRAHAM JM
      RADIOLOGICAL FEATURES IN BRACHMANN-DELANGE SYNDROME

      American journal of medical genetics
    16. PARK JP; MCDERMET MK; MOESCHLER JB; WURSTERHILL DH
      A CASE OF DE-NOVO TRANSLOCATION 7-10 AND THE DUPLICATION 7P, DELETION10P PHENOTYPE

      Annales de genetique


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 15/01/21 alle ore 22:49:40