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La ricerca find articoli where authors phrase all words 'LEBO RV' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 36 riferimenti
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    1. Lebo, RV; Maher, T; Farrer, L; Fenerci, EY; Milunsky, JM
      Highly polymorphic short tandem repeat analyses clarify complex molecular test results

      DIAGNOSTIC MOLECULAR PATHOLOGY
    2. Lebo, RV; Ikuta, T; Milunsky, JM; Milunsky, A
      Rett syndrome from quintuple and triple deletions within the MECP2 deletion hotspot region

      CLINICAL GENETICS
    3. Wyandt, HE; Lebo, RV; Fenerci, EY; Sadhu, DN; Milunsky, JM
      Tandem duplication/deletion in a maternally derived chromosome 9 supernumerary derivative resulting in 9p trisomy and partial 9q tetrasomy

      AMERICAN JOURNAL OF MEDICAL GENETICS
    4. Lebo, RV; Shapiro, LR; Fenerci, EY; Hoover, JM; Chuang, JL; Chuang, DT; Kronn, DF
      Rare etiology of autosomal recessive disease in a child with noncarrier parents

      AMERICAN JOURNAL OF HUMAN GENETICS
    5. Kim, HS; Klimanskaya, IV; Damsky, CK; Pedersen, RA; Lebo, RV
      Preimplantation diagnosis of the beta 1 integrin knockout mutation as a model for aneuploid gene testing

      HUMAN GENETICS
    6. Lebo, RV; Milunsky, J; Higgins, AW; Loose, B; Huang, XL; Wyandt, HE
      Symmetric replication of an unstable isodicentric Xq chromosome derived from isolocal maternal sister chromatid recombination

      AMERICAN JOURNAL OF MEDICAL GENETICS
    7. Hodge, SE; Lebo, RV; Yesley, AR; Cheney, SM; Angle, H; Milunsky, J
      Calculating posterior cystic fibrosis risk with echogenic bowel and one characterized cystic fibrosis mutation: Avoiding pitfalls in the risk calculations

      AMERICAN JOURNAL OF MEDICAL GENETICS
    8. LEBO RV
      PRENATAL-DIAGNOSIS OF CHARCOT-MARIE-TOOTH-DISEASE

      Prenatal diagnosis
    9. KIM HS; MEULISIMMEN C; BUNCKE HJ; LEBO RV
      DNA AMPLIFICATION DETERMINES DONOR-CELL FATE IN CRYOPRESERVED SKIN ALLOGRAFTS

      Journal of reconstructive microsurgery
    10. SAGO H; KIM HS; GOLDBERG JD; CHUNG JH; PEDERSEN RA; LEBO RV
      DUAL BLASTOMERE ANALYSIS IMPROVES RELIABILITY OF PREIMPLANTATION TREMBLER MOUSE DIAGNOSIS

      Human genetics
    11. YU LC; MOORE DH; MAGRANE G; CRONIN J; PINKEL D; LEBO RV; GRAY JW
      OBJECTIVE ANEUPLOIDY DETECTION FOR FETAL AND NEONATAL SCREENING USINGCOMPARATIVE GENOMIC HYBRIDIZATION (CGH)

      Cytometry
    12. SAGO H; CHEN E; CONTE WJ; COX VA; GOLDBERG JD; LEBO RV; GOLABI M
      TRUE TRISOMY-2 MOSAICISM IN AMNIOCYTES AND NEWBORN LIVER ASSOCIATED WITH MULTIPLE SYSTEM ABNORMALITIES

      American journal of medical genetics
    13. PEDERSEN RA; KIM HS; KLIMANSKAYA IV; LEBO RV; DAMSKY CK
      PREIMPLANTATION DIAGNOSIS OF A BETA-1 INTEGRIN TARGETED MUTATION IN MOUSE EMBRYOS

      Fertility and sterility
    14. LEBO RV; SAGO H; KIM HS; GOLDBERG JD; PEDERSEN RA
      DUAL BLASTOMERE ANALYSIS IMPROVES RELIABILITY OF PREIMPLANTATION TREMBLER MOUSE DIAGNOSIS

      American journal of human genetics
    15. SAGO H; GOLDBERG JD; LEBO RV
      POINT MUTATION ANALYSIS OF ARCHIVED CYTOGENETIC SLIDE DNA

      Cytogenetics and cell genetics
    16. RAVNAN JB; CHEN E; GOLABI M; LEBO RV
      CHROMOSOME 22Q11.2 MICRODELETIONS IN VELOCARDIOFACIAL SYNDROME PATIENTS WITH WIDELY VARIABLE MANIFESTATIONS

      American journal of medical genetics
    17. LAPIDOTLIFSON Y; LEBO RV; FLANDERMEYER RR; CHUNG JH; GOLBUS MS
      RAPID ANEUPLOID DIAGNOSIS OF HIGH-RISK FETUSES BY FLUORESCENCE IN-SITU HYBRIDIZATION

      American journal of obstetrics and gynecology
    18. RAVNAN JB; CHEN E; GOLABI M; FLANDERMEYER RR; GOLBUS MS; LEBO RV
      FISH ANALYSIS OF A SHPRINTZEN CLINICAL-SERIES

      Cytogenetics and cell genetics
    19. OHNISHI A; LI LY; FUKUSHIMA Y; MORI T; MORI M; ENDO C; YOSHIMURA T; SONOBE M; FLANDERMEYER R; LEBO RV
      ASIAN HEREDITARY NEUROPATHY PATIENTS WITH PERIPHERAL MYELIN PROTEIN-22 GENE ANEUPLOIDY

      American journal of medical genetics
    20. GOLABI M; SAGO H; CHEN E; CONTE WJ; COX VA; LEBO RV
      TRUE TRISOMY-2 MOSAICISM IN AMNIOCYTES AND NEWBORN LIVER ASSOCIATED WITH MULTIPLE SYSTEM ABNORMALITIES

      American journal of human genetics
    21. KIM HS; MEULISIMMEN C; BUNCKE HJ; LEBO RV
      PCR ANALYSIS REVEALS THE FATE OF SKIN-GRAFTS

      American journal of human genetics
    22. GOLDBERG ID; LEBO RV
      PCR ANALYSIS OF DNA FROM ARCHIVED CYTOGENETIC SLIDES

      American journal of human genetics
    23. BROOKS DG; LEBO RV; RAVETCH JV
      THE HUMAN-IGG RECEPTOR AND CHARCOT-MARIE-TOOTH DISEASE LOCI ON CHROMOSOME-1

      Cytogenetics and cell genetics
    24. MCGINNIS MD; LEBO RV; QUINN DL; SIMONS MJ
      ANCIENT, HIGHLY POLYMORPHIC HUMAN MAJOR HISTOCOMPATIBILITY COMPLEX DQA1 INTRON SEQUENCES

      American journal of medical genetics
    25. KIM JH; LEBO RV; CAI SP; SU X; CHUNG JH; MENTZER WC; GOLBUS MS
      PRENATAL-DIAGNOSIS OF UNUSUAL HEMOGLOBINOPATHIES

      American journal of medical genetics
    26. THOMAS FP; LEBO RV; ROSOKLIJA G; DING XS; LOVELACE RE; LATOV N; HAYS AP
      TOMACULOUS NEUROPATHY IN CHROMOSOME 1 CHARCOT-MARIE-TOOTH SYNDROME

      Acta Neuropathologica
    27. LEBO RV; CHANCE PF; DYCK PJ; REDILAFLORES MT; LYNCH ED; GOLBUS MS; BIRD TD; KING MC; ANDERSON LA; HALL J; WIEGANT J; JIANG ZR; DAZIN PF; PUNNETT HH; SCHONBERG SA; MOORE K; SHULL MM; GENDLER S; HURKO O; LOVELACE RE; LATOV N; TROFATTER J; CONNEALLY PM
      CHROMOSOME 1 CHARCOT-MARIE-TOOTH DISEASE (CMT1B) LOCUS IN THE FC-GAMMA RECEPTOR GENE REGION (VOL 88, PG 1, 1991)

      Human genetics
    28. MANSFIELD ES; ROBERTSON JM; LEBO RV; LUCERO MY; MAYRAND PE; RAPPAPORT E; PARRELLA T; SARTORE M; SURREY S; FORTINA P
      DUCHENNE-BECKER MUSCULAR-DYSTROPHY CARRIER DETECTION USING QUANTITATIVE PCR AND FLUORESCENCE-BASED STRATEGIES

      American journal of medical genetics
    29. LEBO RV; KOERPER MA; KIM JH; CHUEH J; GOLBUS MS
      PRENATAL-DIAGNOSIS OF HEMOPHILIA INVOLVING GRANDPATERNAL MOSAICISM

      American journal of medical genetics
    30. LEBO RV; MARTELLI L; SU Y; LI LY; LYNCH E; MANSFIELD E; PUA KH; WATSON DF; CHUEH J; HURKO O
      PRENATAL-DIAGNOSIS OF CHARCOT-MARIE-TOOTH DISEASE TYPE-1A BY MULTICOLOR IN-SITU HYBRIDIZATION

      American journal of medical genetics
    31. LEBO RV; LYNCH ED; GOLBUS MS; FLANDERMEYER RR; YEN PH; SHAPIRO LJ
      PRENATAL IN-SITU HYBRIDIZATION TEST FOR DELETED STEROID SULFATASE GENE

      American journal of medical genetics
    32. FRIES MH; LEBO RV; SCHONBERG SA; GOLABI M; SELTZER WK; GITELMAN SE; GOLBUS MS
      MENTAL-RETARDATION LOCUS IN XP21 CHROMOSOME MICRODELETION

      American journal of medical genetics
    33. GOLDBERG JD; MARTIN MC; LEBO RV; PEDERSEN RA
      PREIMPLANTATION DIAGNOSIS

      Western journal of medicine
    34. SU Y; BROOKS DG; LI LY; LEPERCQ J; TROFATTER JA; RAVETCH JV; LEBO RV
      MYELIN PROTEIN ZERO GENE MUTATED IN CHARCOT-MARIE-TOOTH TYPE-1B PATIENTS

      Proceedings of the National Academy of Sciences of the United Statesof America
    35. MCGINNIS MD; SIMONS MJ; QUINN DL; LEBO RV
      ANCIENT, HIGHLY INFORMATIVE POLYMORPHISMS IN AN HLA DQA1 INTRON

      American journal of human genetics
    36. LI LY; SU Y; SU X; MARTELLI L; HURKO O; SHAPIRO L; CHUEH J; LEBO RV
      IN-SITU HYBRIDIZATION WITH DIFFERENT COLOR CONTROL PROBE DETERMINES GENE ANEUPLOIDY RELIABLY

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 19/01/21 alle ore 21:47:16