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    1. Elghezal, H; Le Guyader, G; Radford-Weiss, I; Perot, C; Van den Akker, J; Eydoux, P; Vekemans, M; Romana, SP
      Reassessment of childhood B-Lineage lymphoblastic leukemia karyotypes using spectral analysis

      GENES CHROMOSOMES & CANCER
    2. Provencher, DM; Lounis, H; Champoux, L; Tetrault, M; Manderson, EN; Wang, JC; Eydoux, P; Savoie, R; Tonin, PN; Mes-Masson, AM
      Characterization of four novel epithelial ovarian cancer cell lines

      IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL
    3. Wang, JC; Mes-Masson, AM; Tonin, PN; Provencher, D; Eydoux, P
      Trisomy of chromosome 10 in two cases of ovarian carcinoma

      CANCER GENETICS AND CYTOGENETICS
    4. Collins, KA; Eydoux, P; Duncan, AMV; Ortenberg, J; Silver, K; Kaloustian, VMD
      Phenotypic manifestation in a child with 46,X,der(X)t(X;1) (q24;q31.1)

      AMERICAN JOURNAL OF MEDICAL GENETICS
    5. Azancot, A; Eydoux, P; Vuillard, E; Cusin, V; Baumann, C; Blot, P
      Clinical spectrum of antenatal tetralogy of Fallot.

      ARCHIVES DES MALADIES DU COEUR ET DES VAISSEAUX
    6. Winsor, EJT; Tomkins, DJ; Kalousek, D; Farrell, S; Wyatt, P; Fan, YS; Carter, R; Wang, HS; Dallaire, L; Eydoux, P; Welch, JP; Dawson, A; Lin, JCC; Singer, J; Johnson, J; Wilson, RD
      Cytogenetic aspects of the Canadian early and mid-trimester amniotic fluidtrial (CEMAT)

      PRENATAL DIAGNOSIS
    7. AZOUZ EM; TEEBI AS; EYDOUX P; CHEN MF; FASSIER F
      BONE DYSPLASIAS - AN INTRODUCTION

      Canadian Association of Radiologists journal
    8. KASPRZAK L; KALOUSTIAN VMM; ELLIOTT AM; SHEVELL M; LEJTENYI C; EYDOUX P
      DELETION OF 22Q11 IN 2 BROTHERS WITH DIFFERENT PHENOTYPE

      American journal of medical genetics
    9. Daikha-Dahmane, F; Huten, Y; Morvan, J; Szpiro-Tapia, S; Nessmann, C; Eydoux, P
      Fetus with Casamassima-Morton-Nance syndrome and an inherited (6;9) balanced translocation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    10. WILSON RD; JOHNSON JM; DANSEREAU J; SINGER J; DRINNAN SL; WINSOR EJT; SOANES S; KALOUSEK D; HILLIER J; HO MF; BROWN J; WYATT P; FARRELL S; OFARRELL J; CHADWICK D; NATALE R; MITCHELL C; FAN YS; MOHIDE P; BEECROFT ML; TOMKINS DJ; CARTER R; BENZIE R; MACLEAN B; WANG HS; DALLAIRE L; DESROCHERS M; TIHY F; EYDOUX P; PROVENCHER S; CARTIER L; ARMSON BA; HOGG H; WELCH JP; HARMAN C; BABAIAN K; DAWSON A; OKUN N; PARK M; LIN JCC; ROBINSON G; SUMMERS A
      RANDOMIZED TRIAL TO ASSESS SAFETY AND FETAL-OUTCOME OF EARLY AND MIDTRIMESTER AMNIOCENTESIS

      Lancet
    11. TEEBI AS; MILLER S; OSTRER H; EYDOUX P; COLOMBBROCKMANN C; OUDJHANE K; WATTERS G
      SPASTIC PARAPLEGIA, OPTIC ATROPHY, MICROCEPHALY WITH NORMAL INTELLIGENCE, AND XY SEX REVERSAL - A NEW AUTOSOMAL RECESSIVE SYNDROME

      Journal of Medical Genetics
    12. ZHANG XX; TENENHOUSE HS; HEWSON AS; MURER H; EYDOUX P
      ASSIGNMENT OF RENAL-SPECIFIC NA-PHOSPHATE COTRANSPORTER GENE SLC17A2 TO MOUSE-CHROMOSOME BAND 13B BY IN-SITU HYBRIDIZATION()

      Cytogenetics and cell genetics
    13. ZHANG XX; LEONDELRIO A; GRAVEL RA; EYDOUX P
      ASSIGNMENT OF HOLOCARBOXYLASE SYNTHETASE GENE (HLCS) TO HUMAN-CHROMOSOME BAND 21Q22.1 AND TO MOUSE CHROMOSOME BAND 16C4 BY IN-SITU HYBRIDIZATION

      Cytogenetics and cell genetics
    14. ZHANG XX; TENENHOUSE HS; HEWSON AS; EYDOUX P
      ASSIGNMENT OF RENAL SPECIFIC NA-PHOSPHATE COTRANSPORTER GENE SLC17A1 TO MOUSE CHROMOSOME BANDS 13A3-]A4 BY IN-SITU HYBRIDIZATION()

      Cytogenetics and cell genetics
    15. SASI K; SANDERSON D; EYDOUX P; CARTIER L; SCRIVER CR; TREACY E
      PRENATAL-DIAGNOSIS FOR INBORN-ERRORS OF METABOLISM AND HEMOGLOBINOPATHIES - THE MONTREAL-CHILDRENS-HOSPITAL EXPERIENCE

      Prenatal diagnosis
    16. KNOLL KHM; REPETTO G; DERKALOUSTIAN V; MUNDLOS C; EYDOUX P; KORF B; WHITE LM
      LARGE DICENTRIC CHROMOSOME 15Q11Q13 DUPLICATIONS - MULTIPLE REGIONS OF BREAKAGE, MECHANISMS OF FORMATION AND CLINICAL FINDINGS

      American journal of human genetics
    17. BIELANSKA M; WANG JC; LAGOUSAKOS N; BIELANSKA MM; DEMCZUK S; EYDOUX P
      TELOMERIC FISH ANALYSIS - THE USE OF TELOMERIC PROBES FOR THE CHARACTERIZATION OF VISIBLE CHROMOSOME REARRANGEMENTS USING FLUORESCENCE IN-SITU HYBRIDIZATION

      American journal of human genetics
    18. EYDOUX P; HEWSON S; SCARPELLI H; HALAL F; TEEBI AS
      JUBERG-MARSIDI-SYNDROME ASSOCIATED WITH AN INHERITED PARACENTRIC INVERSION OF CHROMOSOME-X

      American journal of human genetics
    19. CARTIER L; RUPPS R; PROVENCHER S; HAMILTON E; MORIN L; KHALIFE S; EYDOUX P
      FETAL KARYOTYPING IN PREGNANCIES WITH CHOROID-PLEXUS CYSTS DETECTED THROUGH ULTRASOUND - RESULTS AND POLICY

      American journal of human genetics
    20. DEMCZUK S; AURIAS A; EYDOUX P
      ESTABLISHMENT OF A TRANSCRIPTION MAP IN THE 22Q11.2 MICRODELETION SYNDROME CRITICAL REGION

      American journal of human genetics
    21. WANG JC; LAGOUSAKOS N; BIELANSKA MM; MESMASSON AM; TONIN P; PROVENCHER D; DEMCZUK S; EYDOUX P
      CHARACTERIZATION OF CLONAL CHROMOSOME REARRANGEMENTS USING FISH IN A CELL-LINE DERIVED FROM OVARIAN EPITHELIAL CANCER (EOC)

      American journal of human genetics
    22. LECLERC D; CAMPEAU E; GOYETTE P; ADJALLA CE; CHRISTENSEN B; ROSS M; EYDOUX P; ROSENBLATT DS; ROZEN R; GRAVEL RA
      HUMAN METHIONINE SYNTHASE - CDNA CLONING AND IDENTIFICATION OF MUTATIONS IN PATIENTS OF THE CBLG COMPLEMENTATION GROUP OF FOLATE COBALAMIN DISORDERS/

      Human molecular genetics
    23. POULIN C; MATTHEWS P; GENGE A; EYDOUX P; SHEVELL M; VANASSE M; SILVER K
      CHILDHOOD HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSY

      Annals of neurology
    24. AZOUZ EM; CHEN MF; KHALIFE S; CARTIER L; EYDOUX P
      NEW FORM OF BONE DYSPLASIA WITH MULTIPLE FRACTURES ASSOCIATED WITH MONOSOMY-X

      American journal of medical genetics
    25. DERKALOUSTIAN VM; KLEIJER W; BOOTH A; AUERBACH AD; MAZER B; ELLIOTT AM; ABISH S; USHER R; WATTERS G; VEKEMANS M; EYDOUX P
      POSSIBLE NEW VARIANT OF NIJMEGEN BREAKAGE SYNDROME

      American journal of medical genetics
    26. RUPPS R; ELLIOTT AM; AZOUZ EM; BERNSTEIN ML; KAPLAN P; EYDOUX P; DERKALOUSTIAN VM
      SKELETAL AND CARDIAC-MALFORMATIONS WITH THROMBOCYTOPENIA - A NEW SYNDROME

      American journal of medical genetics
    27. KAGAN RS; KALOUSTIAN VMD; EYDOUX P; MAZER BD
      CELLULAR IMMUNODEFICIENCY WITH ELEVATED IGE AND A NEW 840 ANOMALY OF CHROMOSOME-22

      Journal of allergy and clinical immunology
    28. TREACY E; POLYCHRONAKOS C; VEKEMANS M; EYDOUX P; BLAICHMAN S; SCARPELLI H; ROSS M; XU YQ; KALOUSTIAN VMD
      TRANSLOCATION BETWEEN CHROMOSOME-6 AND CHROMOSOME-15 (45,XX,T(6-15)(Q25-Q11.2)) WITH FURTHER EVIDENCE FOR LACK OF IMPRINTING OF THE INSULIN-LIKE GROWTH-FACTOR-II MANNOSE-6-PHOSPHATE RECEPTOR IN HUMANS

      Journal of Medical Genetics
    29. ROSENAUER A; RAELSON JV; NERVI C; EYDOUX P; DEBLASIO A; MILLER WH
      ALTERATIONS IN EXPRESSION, BINDING TO LIGAND AND DNA, AND TRANSCRIPTIONAL ACTIVITY OF REARRANGED AND WILD-TYPE RETINOID RECEPTORS IN RETINOID-RESISTANT ACUTE PROMYELOCYTIC LEUKEMIA-CELL LINES

      Blood
    30. DERKALOUSTIAN VM; ELLIOTT AM; EYDOUX P
      SEVERE INTRAUTERINE GROWTH-RETARDATION WITH INCREASED MITOMYCIN-C SENSITIVITY, OR NIJMEGEN BREAKAGE SYNDROME

      Journal of Medical Genetics
    31. ELLIOTT AM; RUPPS R; AZOUZ EM; BERNSTEIN ML; EYDOUX P; KAPLAN P; DERKALOUSTIAN VM
      SKELETAL AND CARDIAC-MALFORMATIONS WITH THROMBOCYTOPENIA - A NEW SYNDROME

      American journal of human genetics
    32. GILPIN CA; ARBOUR L; PEKELES G; PAQUET M; EYDOUX P
      INCREASED RATE OF CONGENITAL HEART-DEFECTS AMONG THE INUIT OF BAFFIN-ISLAND

      American journal of human genetics
    33. VAZKEN M; DERKALOUSTIAN MD; KLEIJER W; VEKEMANS M; MAZER B; ELLIOTT AM; BOOTH A; ABISH S; EYDOUX P
      A NEW VARIANT OF THE NIJMEGEN BREAKAGE SYNDROME WITH MULTIPLE NONSPECIFIC CHROMOSOMAL-ANOMALIES AND A PARTICULAR PHENOTYPE

      American journal of human genetics
    34. EYDOUX P; KASPRZAK L; ELLIOTT AM; SHEVELL M; DERKALOUSTIAN VM
      DE-NOVO DELETION OF 22Q11 IN 2 MALE SIBLINGS WITH DIFFERENT PHENOTYPES

      American journal of human genetics
    35. SASI R; ROSENFELD B; EYDOUX P; TEEBI AS
      HETEROGENEITY OF TRICHOTHIODYSTROPHY-NEUROCUTANEOUS SYNDROME

      American journal of human genetics
    36. ZHANG XX; ROZEN R; HEDIGER MA; GOODYER P; EYDOUX P
      ASSIGNMENT OF THE GENE FOR CYSTINURIA (SLC3A1) TO HUMAN-CHROMOSOME 2P21 BY FLUORESCENCE IN-SITU HYBRIDIZATION

      Genomics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 20/01/21 alle ore 20:45:46