Catalogo Articoli (Spogli Riviste)

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La ricerca find articoli where authors phrase all words ' Cunniff, C' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 41 riferimenti
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    1. Cunniff, C; Frias, JL; Kaye, CI; Moeschler, J; Panny, SR; Trotter, TL
      Health care supervision for children with Williams syndrome

      PEDIATRICS
    2. Cunniff, C; Frias, JL; Kaye, C; Moeschler, JB; Panny, SR; Trotter, TL
      Maternal phenylketonuria

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

      PEDIATRICS
    4. Pujol, LA; Erickson, RP; Heidenreich, RA; Cunniff, C
      Variable presentation of Rothmund-Thomson syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    5. 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
    6. 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
    7. Kaye, CI; Cunniff, C; Frias, JL; Moeschler, J; Panny, SR; Trotter, TL
      Evaluation of the newborn with developmental anomalies of the external genitalia

      PEDIATRICS
    8. Desposito, F; Desposito, F; Cunniff, C; Frias, JL; Panny, SR; Trotter, TL; Wappner, RS; Hanson, JW; Elias, S; Moore, CA; Lloyd-Puryear, M; de la Cruz, F; Pletcher, BA; Cho, SC
      Folic acid for the prevention of neural tube defects

      PEDIATRICS
    9. CUNNIFF C; CURTIS M; HASSED SJ; HOYME HE
      BLEPHAROPHIMOSIS - A CAUSALLY HETEROGENEOUS MALFORMATION FREQUENTLY ASSOCIATED WITH DEVELOPMENTAL-DISABILITIES

      American journal of medical genetics
    10. CURRY CJ; STEVENSON RE; AUGHTON D; BYRNE J; CAREY JC; CASSIDY S; CUNNIFF C; GRAHAM JM; JONES MC; KABACK MM; MOESCHLER J; SCHAEFER GB; SCHWARTZ S; TARLETON J; OPITZ J
      EVALUATION OF MENTAL-RETARDATION - RECOMMENDATIONS OF A CONSENSUS CONFERENCE

      American journal of medical genetics
    11. HASSED S; SHEWMAKE K; TEO C; CURTIS M; CUNNIFF C
      SHPRINTZEN-GOLDBERG SYNDROME WITH OSTEOPENIA AND PROGRESSIVE HYDROCEPHALUS

      American journal of medical genetics
    12. CUNNIFF C; KRATZ LE; MOSER A; NATOWICZ MR; KELLEY RI
      CLINICAL AND BIOCHEMICAL SPECTRUM OF PATIENTS WITH RSH SMITH-LEMLI-OPITZ SYNDROME AND ABNORMAL CHOLESTEROL-METABOLISM/

      American journal of medical genetics
    13. LIN AE; ARDINGER HH; ARDINGER RH; CUNNIFF C; KELLEY RI
      CARDIOVASCULAR MALFORMATIONS IN SMITH-LEMLI-OPITZ SYNDROME

      American journal of medical genetics
    14. IDEN S; CUNNIFF C; STORM A; HOYME HE; ATKINSON M; BYERS P
      EHLERS-DANLOS-SYNDROME TYPE VIIA WITH RECURRENT FRACTURES AND MACROCEPHALY

      American journal of human genetics
    15. BASERDECKER T; CUNNIFF C; HAUCK L; HOYME HE
      COMPLETE EXPRESSION AND NORMAL FERTILITY IN A WOMAN WITH X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA WITH T(X-19)

      Journal of investigative medicine
    16. FRIEDMAN BD; CUNNIFF C; HEIDENREICH RA; JONES JL; HOYME HE
      THE ETIOLOGIC HETEROGENEITY OF PENILE AGENESIS

      Journal of investigative medicine
    17. RICKERT VI; HASSED SJ; HENDON AE; CUNNIFF C
      THE EFFECTS OF PEER RIDICULE ON DEPRESSION AND SELF-IMAGE AMONG ADOLESCENT FEMALES WITH TURNER SYNDROME

      Journal of adolescent health
    18. CUNNIFF C; BASERDECKER T; HAUCK L; HOYME HE
      COMPLETE EXPRESSION AND NORMAL FERTILITY IN A WOMAN WITH X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA ASSOCIATED WITH T(X-19)

      Pediatric research
    19. CUNNIFF C; KRATZ LE; MOSER A; NATOWICZ MR; KELLEY RI
      CLINICAL SPECTRUM OF PATIENTS WITH RSH SMITH-LEMLI-OPTIZ SYNDROME/

      Pediatric research
    20. SAWYER JR; SWANSON CM; WHEELER G; CUNNIFF C
      CHROMOSOME INSTABILITY IN ICF SYNDROME - FORMATION OF MICRONUCLEI FROM MULTIBRANCHED CHROMOSOMES-1 DEMONSTRATED BY FLUORESCENCE IN-SITU HYBRIDIZATION

      American journal of medical genetics
    21. CUNNIFF C; CARMACK JL; KIRBY RS; FISER DH
      CONTRIBUTION OF HERITABLE DISORDERS TO MORTALITY IN THE PEDIATRIC INTENSIVE-CARE UNIT

      Pediatrics
    22. CUNNIFF C; HASSED SJ; HENDON AE; RICKERT VI
      HEALTH-CARE UTILIZATION AND PERCEPTIONS OF HEALTH AMONG ADOLESCENTS AND ADULTS WITH TURNER SYNDROME

      Clinical genetics
    23. HOYME HE; CUNNIFF C; HAUCK L
      TOWARD A MORE RATIONAL CLASSIFICATION OF ALCOHOL-RELATED BIRTH-DEFECTS - ANALYSIS OF 437 CHILDREN AND ADULTS WITH PRENATAL ALCOHOL EXPOSURE

      American journal of human genetics
    24. HASSED SJ; SHEWMAKE K; TEO C; CUNNIFF C; CURTIS MA
      SHPRINTZEN-GOLDBERG SYNDROME WITH NEONATAL FRACTURES AND CHILDHOOD WET OF HYDROCEPHALUS

      American journal of human genetics
    25. PENNY LA; DELLAQUILA M; JONES MC; BERGOFFEN JA; CUNNIFF C; FRYNS JP; GRACE E; GRAHAM JM; KOUSSEFF B; MATTINA T; SYME J; VOULLAIRE L; ZELANTE L; ZENGERHAIN J; JONES OW; EVANS GA
      CLINICAL AND MOLECULAR CHARACTERIZATION OF PATIENTS WITH DISTAL 11Q DELETIONS

      American journal of human genetics
    26. HUDOME SM; KIRBY RS; SENNER JW; CUNNIFF C
      CONTRIBUTION OF GENETIC-DISORDERS TO NEONATAL-MORTALITY IN A REGIONALINTENSIVE-CARE SETTING

      American journal of perinatology
    27. SAWYER JR; JONES E; HAWKS FF; QUIRK JG; CUNNIFF C
      DUPLICATION AND DELETION OF CHROMOSOME BAND 2(P21P22) RESULTING FROM A FAMILIAL INTERSTITIAL INSERTION (211)(P21P15)

      American journal of medical genetics
    28. CUNNIFF C; KIRBY RS; SENNER JW; CANINO C; BREWSTER MA; BUTLER B; HASSED SJ; MURPHY P
      DEATHS ASSOCIATED WITH RENAL AGENESIS - A POPULATION-BASED STUDY OF BIRTH PREVALENCE, CASE ASCERTAINMENT, AND ETIOLOGIC HETEROGENEITY

      Teratology
    29. CUNNIFF C; KIRBY R; SENNER J; CANINO C; BREWSTER M; BUTLER B; HASSED S
      RENAL AGENESIS DYSGENESIS - A POPULATION-BASED STUDY OF BIRTH PREVALENCE, CASE ASCERTAINMENT AND ETIOLOGIC HETEROGENEITY

      Pediatric research
    30. CUNNIFF C; MARKLEY R; FEILD CR
      FETAL ALCOHOL SYNDROME SURVEILLANCE - EPSDT SCREENING

      Pediatric research
    31. BRODSKY MC; CUNNIFF C
      OCULAR ANOMALIES IN THE ALAGILLE SYNDROME (ARTERIOHEPATIC DYSPLASIA)

      Ophthalmology
    32. 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
    33. CUNNIFF C; CURRY CJR; CAREY JC; GRAHAM JM; WILLIAMS CA; STENGELRUTKOWSKI S; LUTTGEN S; MEINECKE P
      CONGENITAL DIAPHRAGMATIC-HERNIA IN THE BRACHMANN-DELANGE SYNDROME

      American journal of medical genetics
    34. CUNNIFF C; POPE SK
      MALFORMATIONS AND MINOR ANOMALIES IN NON-TRISOMIC, AUTOSOMAL ANEUPLOIDY

      American journal of medical genetics
    35. BRODSKY M; CUNNIFF C
      GENETICS OF AICARDI SYNDROME - REPLY

      Survey of ophthalmology
    36. CARNEY SH; BRODSKY MC; GOOD WV; GLASIER CM; GREIBEL ML; CUNNIFF C
      AICARDI SYNDROME - MORE THAN MEETS THE EYE

      Survey of ophthalmology
    37. CUNNIFF C; WILLIAMSONKRUSE L; OLNEY AH
      CONGENITAL MICROGASTRIA AND LIMB REDUCTION DEFECTS

      Pediatrics
    38. HASSED SJ; MILLER CH; POPE SK; MURPHY P; QUIRK JG; CUNNIFF C
      PERINATAL LETHAL CONDITIONS - THE EFFECT OF DIAGNOSIS ON DECISION-MAKING

      Obstetrics and gynecology
    39. CARMACK J; FISER DH; KIRBY RS; CUNNIFF C
      GENETIC CONTRIBUTION TO MORTALITY IN A REGIONAL PEDIATRIC INTENSIVE-CARE UNIT SETTING

      Clinical research
    40. CUNNIFF C; KIRBY RS; SENNER JW; CANINO C; BREWSTER M; BUTLER B; HASSED SJ
      RENAL AGENESIS DYSGENESIS - A POPULATION-BASED STUDY OF BIRTH PREVALENCE, CASE ASCERTAINMENT AND ETIOLOGIC HETEROGENEITY

      Clinical research
    41. CUNNIFF C; HASSED SJ; HENDON AE; RICKERT VI
      HEALTH-STATUS AND HEALTH-CARE UTILIZATION IN ADOLESCENTS AND ADULTS WITH TURNER SYNDROME

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 15/01/21 alle ore 23:27:28