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La ricerca find articoli where soggetti phrase all words 'ECTRODACTYLY' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 39 riferimenti
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    1. Witters, I; Devriendt, K; Moerman, P; Caudron, J; Van Hole, C; Fryns, JP
      Bilateral tibial agenesis with ectrodactyly (OMIM 119100): Further evidence for autosomal recessive inheritance

      AMERICAN JOURNAL OF MEDICAL GENETICS
    2. Senecky, Y; Halpern, GJ; Inbar, D; Attias, J; Shohat, M
      Ectodermal dysplasia, ectrodactyly and macular dystrophy (EEM syndrome) insiblings

      AMERICAN JOURNAL OF MEDICAL GENETICS
    3. Sifakis, S; Basel, D; Ianakiev, P; Kilpatrick, MW; Tsipouras, P
      Distal limb malformations: underlying mechanisms and clinical associations

      CLINICAL GENETICS
    4. Katayama, K; Ishigami, N; Suzuki, M; Ohtsuka, R; Kiatipattanasakul, W; Nakayama, H; Doi, K
      Teratologic studies on rat perinates and offspring from dams treated with ethylnitrosourea (ENU)

      EXPERIMENTAL ANIMALS
    5. Montgomery, TL; Wyllie, J; Oley, C
      Ectrodactyly and glaucoma associated with a 7q21.2-q31.2 interstitial deletion

      CLINICAL DYSMORPHOLOGY
    6. Guion-Almeida, ML; Zechi-Ceide, RM; Richieri-Costa, A
      Cleft lip/palate, abnormal ears, ectrodactyly, congenital heart defect, and growth retardation: definition of the acro-cardio-facial syndrome

      CLINICAL DYSMORPHOLOGY
    7. Mishra, P; Muranjan, M; Bharucha, BA
      Autosomal dominant ectrodactyly with sensorineural deafness

      CLINICAL DYSMORPHOLOGY
    8. Propping, P; Friedl, W; Wienker, TF; Uhlhaas, S; Zerres, K
      ADULT syndrome allelic to limb mammary syndrome (LMS)?

      AMERICAN JOURNAL OF MEDICAL GENETICS
    9. Weimer, J; Kiechle, M; Wiedemann, U; Tonnies, H; Neitzel, H; Ruhenstroth, E; Ovens-Raeder, A; Arnold, N
      Delineation of a complex karyotypic rearrangement by microdissection and CGH in a family affected with split foot

      JOURNAL OF MEDICAL GENETICS
    10. SUTTON C; MCIVOR RS; VAGT M; DOGGETT B; KAPUR RP
      METHOTREXATE-RESISTANT FORM OF DIHYDROFOLATE-REDUCTASE PROTECTS TRANSGENIC MURINE EMBRYOS FROM TERATOGENIC EFFECTS OF METHOTREXATE

      PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
    11. RIZOS M; NEGRON RJ; SERMAN N
      MOBIUS-SYNDROME WITH DENTAL INVOLVEMENT - A CASE-REPORT AND LITERATURE-REVIEW

      The Cleft palate-craniofacial journal
    12. IMAIZUMI K; ISHII T; MASUNO M; KUROKI Y
      ASSOCIATION OF HOLOPROSENCEPHALY, ECTRODACTYLY, CLEFT-LIP CLEFT-PALATE AND HYPERTELORISM - A POSSIBLE 3RD CASE

      Clinical dysmorphology
    13. SOUKA AP; SNIJDERS RJM; NOVAKOV A; SOARES W; NICOLAIDES KH
      DEFECTS AND SYNDROMES IN CHROMOSOMALLY NORMAL FETUSES WITH INCREASED NUCHAL TRANSLUCENCY THICKNESS AT 10-14 WEEKS OF GESTATION

      Ultrasound in obstetrics & gynecology
    14. IRELAND IA; MEYER DR
      OPHTHALMIC MANIFESTATIONS OF ECTRODACTYLY-ECTODERMAL DYSPLASIA-CLEFTING SYNDROME

      Ophthalmic plastic and reconstructive surgery
    15. BAMSHAD M; OQUINN JR; CAREY JC
      WOLF-HIRSCHKORN-SYNDROME AND A SPLIT-HAND MALFORMATION

      American journal of medical genetics
    16. DEJONG G; KIRBY PA; MULLER LM
      RSH-(SMITH-LEMLI-OPITZ)-SYNDROME - SEVERE PHENOTYPE WITH ECTRODACTYLY

      American journal of medical genetics
    17. TRUEB RM; TSAMBAOS D; SPYCHER MA; MULLER J; BURG G
      SCARRING FOLLICULITIS IN THE ECTRODACTYLY-ECTODERMAL DYSPLASIA-CLEFTING SYNDROME - HISTOLOGIC, SCANNING ELECTRON-MICROSCOPIC AND BIOPHYSICAL STUDIES OF HAIR

      Dermatology
    18. CHAOUI R; TENNSTEDT C; GOLDNER B; BOLLMANN R
      PRENATAL-DIAGNOSIS OF VENTRICULO-CORONARY COMMUNICATIONS IN A 2ND-TRIMESTER FETUS USING TRANSVAGINAL AND TRANSABDOMINAL COLOR DOPPLER SONOGRAPHY

      Ultrasound in obstetrics & gynecology
    19. BELL SM; SCHREINER CM; RESNICK E; VORHEES C; SCOTT WJ
      EXACERBATION OF ACETAZOLAMIDE TERATOGENESIS BY AMILORIDE AND ITS ANALOGS ACTIVE AGAINST NA+ H+ EXCHANGERS AND NA+ CHANNELS/

      Reproductive toxicology
    20. SCOTT WJ; SCHREINER CM; NAU H; VORHEES CV; BELILES RP; COLVIN J; MCCANDLESS D
      VALPROATE-INDUCED LIMB MALFORMATIONS IN MICE ASSOCIATED WITH REDUCTION OF INTRACELLULAR PH

      Reproductive toxicology
    21. BOHRING A; OPPERMANN HC
      A FURTHER CASE OF VERTICAL TRANSMISSION OF PROXIMAL FEMORAL FOCAL DEFICIENCY

      American journal of medical genetics
    22. OUELLET M; BONIN J; RODRIGUE J; DESGRANGES JL; LAIR S
      HINDLIMB DEFORMITIES (ECTROMELIA, ECTRODACTYLY) IN FREE-LIVING ANURANS FROM AGRICULTURAL HABITATS

      Journal of wildlife diseases
    23. PRATSCHKE K
      A CASE OF ECTRODACTYLY IN A DOG

      Irish veterinary journal
    24. MAJEWSKI F; GOECKE T; MEINECKE P
      ECTRODACTYLY AND ABSENCE (HYPOPLASIA) OF THE TIBIA - ARE THERE DOMINANT AND RECESSIVE TYPES

      American journal of medical genetics
    25. RAASROTHSCHILD A; MANOUVRIER S; GONZALES M; FARRIAUX JP; LYONNET S; MUNNICH A
      REFINED MAPPING OF A GENE FOR SPLIT HAND SPLIT FOOT MALFORMATION (SHFM3) ON CHROMOSOME 10Q25

      Journal of Medical Genetics
    26. ZENTENO JC; AGUINAGA M; CHAVEZ V; SASTRE N; RIVERA MR; KOFMANALFARO S
      TRIPHALANGEAL THUMB AND BRACHYECTRODACTYLY SYNDROME - AN UNCOMMON ENTITY WITH EVIDENCE OF GEOGRAPHIC-DISTRIBUTION

      Clinical genetics
    27. EVLIYAOGLU N; TEMOCIN AK; ALTINTAS DU; DUMAN N; SATAR N; SULEYMANOVA D
      PHOCOMELIA, ECTRODACTYLY, SKULL DEFECT AND URINARY SYSTEM ANOMALY - SCHINZEL-PHOCOMELIA SYNDROME

      Clinical genetics
    28. CORREACERRO L; GARCIACRUZ D; DIAZCASTANOS L; FIGUERA LE; SANCHEZCORONA J
      INTERSTITIAL DELETION 6Q16.2Q22.2 IN A CHILD WITH ECTRODACTYLY

      Annales de genetique
    29. CAMACHO FM; GATA I
      HYPOTRICHOSIS AND LOOSE ANAGEN HAIR IN EEC (ECTRODACTYLY, ECTODERMAL DYSPLASIA, CLEFT-LIP PALATE) SYNDROME

      EJD. European journal of dermatology
    30. LEUNG KY; MACLACHLAN NA; SEPULVEDA W
      PRENATAL-DIAGNOSIS OF ECTRODACTYLY - THE LOBSTER CLAW ANOMALY

      Ultrasound in obstetrics & gynecology
    31. LURIE IW
      FURTHER STUDY OF GENETIC INTERACTIONS - LOSS OF SHORT ARM MATERIAL INPATIENTS WITH RING CHROMOSOME-4 CHANGES DEVELOPMENTAL PATTERN OF DEL(4)(Q33)

      American journal of medical genetics
    32. MCELVEEN C; CARVAJAL MV; MOSCATELLO D; TOWNER J; LACASSIE Y
      ECTRODACTYLY AND PROXIMAL INTERMEDIATE INTERSTITIAL DELETION 7Q

      American journal of medical genetics
    33. PAES BA
      DISCORDANT FIBULAR APLASIA IN TWINS

      American journal of medical genetics
    34. MARINONI JC; STEVENSON RE; EVANS JP; GESHURI D; PHELAN MC; SCHWARTZ CE
      SPLIT FOOD AND DEVELOPMENTAL RETARDATION ASSOCIATED WITH A DELETION OF 3 MICROSATELLITE MARKERS IN 7Q21.2-Q22.1

      Clinical genetics
    35. TRAUTMANN U; PFEIFFER RA
      INTERSTITIAL DELETION 12P13.1-13.3 IN A MILDLY RETARDED INFANT WITH UNILATERAL ECTRODACTYLY

      Annales de genetique
    36. 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
    37. GENUARDI M; POMPONI MG; SAMMITO V; BELLUSSI A; ZOLLINO M; NERI G
      SPLIT HAND SPLIT FOOT ANOMALY IN A FAMILY SEGREGATING A BALANCED TRANSLOCATION WITH BREAKPOINT ON 7Q22.1

      American journal of medical genetics
    38. NARITOMI K; IZUMIKAWA Y; TOHMA T; HIRAYAMA K
      INVERTED INSERTION OF CHROMOSOME-7Q AND ECTRODACTYLY

      American journal of medical genetics
    39. WOLLINA U; SCHAARSCHMIDT H; ROTH H
      ONYCHOPATHY AS A SIGN OF ECTODERMAL DYSPL ASIAS AND RELATED SYNDROMES

      Hautarzt


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 23/10/20 alle ore 23:41:58