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La ricerca find articoli where authors phrase all words ' Hoyme, HE' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 25 riferimenti
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    1. Olney, RS; Hoyme, HE; Roche, F; Ferguson, K; Hintz, S; Madan, A
      Limb/pelvis hypoplasia/aplasia with skull defect (Schinzel phocomelia): Distinctive features and prenatal detection

      AMERICAN JOURNAL OF MEDICAL GENETICS
    2. Hoyme, HE
      A clinical genetics and dysmorphology approach to growth deficiency

      PEDIATRIC ANNALS
    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. HOYME HE; HAUCK L; QUINN D
      MINOR ANOMALIES ACCOMPANYING PRENATAL EXPOSURE TO TOPIRAMATE

      Journal of investigative medicine
    6. HOYME HE; OGDEN AS; ENNS G; GOLABI M
      A NEW DOMINANT OVERGROWTH SYNDROME - PRENATAL ONSET GROWTH EXCESS, MACROCEPHALY, SPARSE SCALP HAIR, ECZEMA, EXOTROPIA, LARGE HANDS AND FEET, HYPEREXTENSIBILITY AND DEVELOPMENTAL DELAY

      Journal of investigative medicine
    7. HOYME HE; SEAVER LH; JONES KL; PROCOPIO F; CROOKS W; FEINGOLD M
      ISOLATED HEMIHYPERPLASIA (HEMIHYPERTROPHY) - REPORT OF A PROSPECTIVE MULTICENTER STUDY OF THE INCIDENCE OF NEOPLASIA AND REVIEW

      American journal of medical genetics
    8. CUNNIFF C; CURTIS M; HASSED SJ; HOYME HE
      BLEPHAROPHIMOSIS - A CAUSALLY HETEROGENEOUS MALFORMATION FREQUENTLY ASSOCIATED WITH DEVELOPMENTAL-DISABILITIES

      American journal of medical genetics
    9. HOYME HE
      ANTENATAL DETECTION OF HEREDITARY DISORDERS, BY NADLER,HENRY,L., MD, PEDIATRICS, 1968-42 912-918 - COMMENTARY/

      Pediatrics (Evanston)
    10. Witte, MH; Erickson, R; Bernas, M; Andrade, M; Reiser, F; Conlon, W; Hoyme, HE; Witte, CL
      Phenotypic and genotypic heterogeneity in familial Milroy lymphedema

      LYMPHOLOGY
    11. TORIELLO HV; CAREY JC; SUSLAK E; DESPOSITO FR; LEONARD B; LIPSON M; FRIEDMAN BD; HOYME HE
      6 PATIENTS WITH ORAL-FACIAL-DIGITAL SYNDROME-IV - THE CASE FOR HETEROGENEITY

      American journal of medical genetics
    12. 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
    13. 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
    14. FRIEDMAN BD; CUNNIFF C; HEIDENREICH RA; JONES JL; HOYME HE
      THE ETIOLOGIC HETEROGENEITY OF PENILE AGENESIS

      Journal of investigative medicine
    15. 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
    16. BIRD LM; BILLMAN GF; LACRO RV; SPICER RL; JARIWALA LK; HOYME HE; ZAMORASALINAS R; MORRIS C; VISKOCHIL D; FRIKKE MJ; JONES MC
      SUDDEN-DEATH IN WILLIAMS-SYNDROME - REPORT OF 10 CASES

      The Journal of pediatrics
    17. 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
    18. FRIEDMAN BD; CUNNIFF CM; HASSED SJ; HOYME HE
      CONGENITAL PRESENTATION OF NEUROFIBROMATOSIS, TYPE-I, IN 4 UNRELATED CASES SUPPORTS A ROLE FOR NEUROFIBROMIN DURING EARLY MORPHOGENESIS

      American journal of human genetics
    19. LUBINSKY MS; KAHLER SG; SPEER IE; HOYME HE; KIRILLOVA IA; LURIE IW
      VON VOSS-CHERSTVOY SYNDROME - A VARIABLE PERINATALLY LETHAL SYNDROME OF MULTIPLE CONGENITAL-ANOMALIES

      American journal of medical genetics
    20. PEARSON MA; HOYME HE; SEAVER LH; RIMSZA ME
      TOLUENE EMBRYOPATHY - DELINEATION OF THE PHENOTYPE AND COMPARISON WITH FETAL ALCOHOL SYNDROME

      Pediatrics
    21. FRIEDMAN BD; HOYME HE
      VARIABILITY IN THE MYOPATHY OF THE NOONAN KING SYNDROMES

      Clinical research
    22. GREBE TA; RIMSZA ME; RICHTER SF; HANSEN RC; HOYME HE
      FURTHER DELINEATION OF THE EPIDERMAL NEVUS SYNDROME - 2 CASES WITH NEW FINDINGS AND LITERATURE-REVIEW

      American journal of medical genetics
    23. PEREZAYTES A; GRAHAM JM; HERSH JH; HOYME HE; ALECK K; CAREY JC
      URETHRAL OBSTRUCTION SEQUENCE AND LOWER-LIMB DEFICIENCY - EVIDENCE FOR THE VASCULAR DISRUPTION HYPOTHESIS

      The Journal of pediatrics
    24. HOYME HE
      MINOR ANOMALIES - DIAGNOSTIC CLUES TO ABERRANT HUMAN MORPHOGENESIS

      Genetica
    25. HOYME HE; SEAVER LH; BYERS PH
      FAMILIAL HYPERPHOSPHATASEMIA - EVIDENCE OF PROGRESSIVE BONY DEFORMITYDESPITE LONG-TERM HUMAN THYROCALCITONIN THERAPY

      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 22:55:16