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    1. Leppig, KA; Disteche, CM
      Ring X and other structural X chromosome abnormalities: X inactivation andphenotype

      SEMINARS IN REPRODUCTIVE MEDICINE
    2. van Bokhoven, A; Varella-Garcia, M; Korch, C; Hessels, D; Miller, GJ
      Widely used prostate carcinoma cell lines share common origins

      PROSTATE
    3. Anderlid, BM; Sahlen, S; Schoumans, J; Holmberg, E; Ahsgren, I; Mortier, G; Speleman, F; Blennow, E
      Detailed characterization of 12 supernumerary ring chromosomes using micro-FISH and search for uniparental disomy

      AMERICAN JOURNAL OF MEDICAL GENETICS
    4. Shim, SH; Lee, CH; Park, YJ; Lee, HJ; Park, WI; Cho, YH
      Two inv dup(15) chromosomes in a woman with repeated abortions

      AMERICAN JOURNAL OF MEDICAL GENETICS
    5. Finelli, P; Cavalli, P; Giardino, D; Gottardi, G; Natacci, F; Savasta, S; Larizza, L
      FISH characterization of a supernumerary r(1)(:: cen -> q22 :: q22 -> sq21::) chromosome associated with multiple anomalies and bilateral cataracts

      AMERICAN JOURNAL OF MEDICAL GENETICS
    6. Cockwell, AE; Davalos, IP; Rivera, HR; Crolla, JA
      FISH characterization of dynamic mosaicism involving an inv dup(15) in a patient with mental retardation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    7. Dawson, AJ; Konkin, D; Riordan, D; Chudley, AE
      Mosaic trisomy of a small r(1) with an abnormal phenotype

      AMERICAN JOURNAL OF MEDICAL GENETICS
    8. Jalal, SM; Law, ME; Lindor, NM; Thompson, KJ; Sekhon, GS
      Application of multicolor fluorescent in situ hybridization for enhanced characterization of chromosomal abnormalities in congenital disorders

      MAYO CLINIC PROCEEDINGS
    9. Stankiewicz, P; Park, SS; Holder, SE; Waters, CS; Palmer, RW; Berend, SA; Shaffer, LG; Potocki, L; Lupski, JR
      Trisomy 17p10-p12 resulting from a supernumerary marker chromosome derivedfrom chromosome 17: molecular analysis and delineation of the phenotype

      CLINICAL GENETICS
    10. Cervantes, A; Guevara-Yanez, R; Lopez, M; Monroy, N; Aguinaga, M; Valdez, H; Sierra, C; Canun, S; Guizar, J; Navarrete, C; Zafra, G; Salamanca, F; Kofman-Alfaro, S
      PCR-PRINS-FISH analysis of structurally abnormal sex chromosomes in eight patients with Turner phenotype

      CLINICAL GENETICS
    11. Pergament, E
      New molecular techniques for chromosome analysis

      BEST PRACTICE & RESEARCH IN CLINICAL OBSTETRICS & GYNAECOLOGY
    12. Takeda, Y; Baba, A; Nakamura, F; Ito, M; Honma, H; Koyama, T
      Symptomatic generalized epilepsy associated with an inverted duplication of chromosome 15

      SEIZURE-EUROPEAN JOURNAL OF EPILEPSY
    13. Sirvent, N; Forus, A; Lescaut, W; Burel, F; Benzaken, S; Chazal, M; Bourgeon, A; Vermeesch, JR; Myklebost, O; Turc-Carel, C; Ayraud, N; Coindre, JM; Pedeutour, F
      Characterization of centromere alterations in liposarcomas

      GENES CHROMOSOMES & CANCER
    14. Saffery, R; Irvine, DV; Griffiths, B; Kalitsis, P; Wordeman, L; Choo, KHA
      Human centromeres and neocentromeres show identical distribution patterns of > 20 functionally important kinetochore-associated proteins

      HUMAN MOLECULAR GENETICS
    15. Turner, C; Dennis, NR; Skuse, DH; Jacobs, PA
      Seven ring (X) chromosomes lacking the XIST locus, six with an unexpectedly mild phenotype

      HUMAN GENETICS
    16. Weimer, J; Kiechle, M; Arnold, N
      FISH-microdissection (FISH-MD) analysis of complex chromosome rearrangements

      CYTOGENETICS AND CELL GENETICS
    17. Tan-Sindhunata, G; Castedo, S; Leegte, B; Mulder, I; van der Veen, AYV; van der Hout, AHV; Wiersma, TJ; van Essen, AJ
      Molecular cytogenetic characterization of a small, familial supernumerary ring chromosome 7 associated with mental retardation and an abnormal phenotype

      AMERICAN JOURNAL OF MEDICAL GENETICS
    18. Austin-Ward, ED; Castillo, S; Dragnic, Y; Sanz, P; Salazar, S; Knoll, JHM
      Clinical findings in a patient mosaic for a supernumerary ring chromosome 20

      AMERICAN JOURNAL OF MEDICAL GENETICS
    19. Tonk, VS; Kukolich, MK; Morgan, D; Khan, A; Jalal, SM
      Ring chromosome 8 syndrome: Further characterization

      AMERICAN JOURNAL OF MEDICAL GENETICS
    20. 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
    21. Stankiewicz, P; Bocian, E; Jakubow-Durska, K; Obersztyn, E; Lato, E; Starke, H; Mroczek, K; Mazurczak, T
      Identification of supernumerary marker chromosomes derived from chromosomes 5, 6, 19, and 20 using FISH

      JOURNAL OF MEDICAL GENETICS
    22. Wandstrat, AE; Schwartz, S
      Isolation and molecular analysis of inv dup(15) and construction of a physical map of a common breakpoint in order to elucidate their mechanism of formation

      CHROMOSOMA
    23. Weisberg, E; Griffin, JD
      Mechanism of resistance to the ABL tyrosine kinase inhibitor STI571 in BCR/ABL-transformed hematopoietic cell lines

      BLOOD
    24. Schwartz, S
      Molecular cytogenetics: Show me the colors

      GENETICS IN MEDICINE
    25. Jalal, SM; Law, ME
      Utility of multicolor fluorescent in situ hybridization in clinical cytogenetics

      GENETICS IN MEDICINE
    26. PEDEUTOUR F; FORUS A; COINDRE JM; BERNER JM; NICOLO G; MICHIELS JF; TERRIER P; RANCHEREVINCE D; COLLIN F; MYKLEBOST O; TURCCAREL C
      STRUCTURE OF THE SUPERNUMERARY RING AND GIANT ROD CHROMOSOMES IN ADIPOSE-TISSUE TUMORS

      Genes chromosomes & cancer (Print)
    27. Chudoba, I; Franke, Y; Senger, G; Sauerbrei, G; Demuth, S; Beensen, V; Neumann, A; Hansmann, I; Claussen, U
      Maternal UPD 20 in a hyperactive child with severe growth retardation

      EUROPEAN JOURNAL OF HUMAN GENETICS
    28. Haig, D
      A brief history of human autosomes

      PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    29. Drexler, HG; Dirks, WG; MacLeod, RAF
      False human hematopoietic cell lines: cross-contaminations and misinterpretations

      LEUKEMIA
    30. Gisselsson, D; Hoglund, M; Mertens, F; Johansson, B; Dal Cin, P; Van den Berghe, H; Earnshaw, WC; Mitelman, F; Mandahl, N
      The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells

      HUMAN GENETICS
    31. Hastings, RJ; Nisbet, DL; Waters, K; Spencer, T; Chitty, LS
      Prenatal detection of extra structurally abnormal chromosomes (ESACs): Newcases and a review of the literature

      PRENATAL DIAGNOSIS
    32. Ning, Y; Laundon, CH; Schrock, E; Buchanan, P; Ried, T
      Prenatal diagnosis of a mosaic extra structurally abnormal chromosome by spectral karyotyping

      PRENATAL DIAGNOSIS
    33. Reichenbach, H; Holland, H; Dalitz, E; Demandt, C; Meiner, A; Chudoba, I; Lemke, J; Claussen, U; Froster, UG
      De novo complete trisomy 5p: Clinical report and FISH studies

      AMERICAN JOURNAL OF MEDICAL GENETICS
    34. Voullaire, L; Saffery, R; Davies, J; Earle, E; Kalitsis, P; Slater, H; Irvine, DV; Choo, KHA
      Trisomy 20p resulting from inverted duplication and neocentromere formation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    35. Giardino, D; Bettio, D; Gottardi, G; Rizzi, N; Pierluigi, M; Perfumo, C; Cali, A; Bricarelli, FD; Larizza, L
      FISH characterization of two supernumerary r(1) associated with distinct clinical phenotypes

      AMERICAN JOURNAL OF MEDICAL GENETICS
    36. Silver, RK; Blum, K; Geibel, LJ; Beaird, JA; Salafsky, I; MacGregor, SN
      Clinical implications of atypical chromosome abnormalities diagnosed prenatally

      OBSTETRICS AND GYNECOLOGY
    37. Shanske, AL; Dowling, P; Schmidt, R; White, BJ; Russell, B; Bogdanov, A; Marion, RW
      Simultaneous occurrence of two supernumerary autosomal ring chromosomes r(1) and r(16) in twins

      JOURNAL OF MEDICAL GENETICS
    38. Robinson, DO; Dalton, P; Jacobs, PA; Mosse, K; Power, MM; Skuse, DH; Crolla, JA
      A molecular and FISH analysis of structurally abnormal Y chromosomes in patients with Turner syndrome

      JOURNAL OF MEDICAL GENETICS
    39. Uhrig, S; Schuffenhauer, S; Fauth, C; Wirtz, A; Daumer-Haas, C; Apacik, C; Cohen, M; Muller-Navia, J; Cremer, T; Murken, J; Speicher, MR
      Multiplex-FISH for pre- and postnatal diagnostic applications

      AMERICAN JOURNAL OF HUMAN GENETICS
    40. YAMADERA H; KOBAYASHI K; SUGAI K; SUDA H; KANEKO S
      A STUDY OF RING-20 CHROMOSOME KARYOTYPE WITH EPILEPSY

      PSYCHIATRY AND CLINICAL NEUROSCIENCES
    41. Levy, B; Dunn, TM; Kaffe, S; Kardon, N; Hirschhorn, K
      Clinical applications of comparative genomic hybridization

      GENETICS IN MEDICINE
    42. YAN YS; FENG S; WANG YH; ZHANG T
      COMPARISON OF INFECTION FREQUENCIES IN FETUS BY MATERNAL ASCITIC CANCER AND LEUKEMIA-CELLS

      Chinese Science Bulletin
    43. RIED T; SCHROCK E; NING Y; WIENBERG J
      CHROMOSOME PAINTING - A USEFUL ART

      Human molecular genetics (Print)
    44. PAOLONIGIACOBINO A; MORRIS MA; DAHOUN SP
      PRENATAL SUPERNUMERARY R(16) CHROMOSOME CHARACTERIZED BY MULTIPROBE FISH WITH NORMAL-PREGNANCY OUTCOME

      Prenatal diagnosis
    45. OSIPOVA GR; KARMANOV ME; KOZLOVA SI; EVGRAFOV OV
      PCR DETECTION OF Y-SPECIFIC SEQUENCES IN PATIENTS WITH ULLRICH-TURNER-SYNDROME - CLINICAL IMPLICATIONS AND LIMITATIONS

      American journal of medical genetics
    46. SCHROER RJ; PHELAN MC; MICHAELIS RC; CRAWFORD EC; SKINNER SA; CUCCARO M; SIMENSEN RJ; BISHOP J; SKINNER C; FENDER D; STEVENSON RE
      AUTISM AND MATERNALLY DERIVED ABERRATIONS OF CHROMOSOME 15Q

      American journal of medical genetics
    47. VIERSBACH R; ENGELS H; GAMERDINGER U; HANSMANN M
      DELINEATION OF SUPERNUMERARY MARKER CHROMOSOMES IN 38 PATIENTS

      American journal of medical genetics
    48. CROLLA JA; LONG F; RIVERA H; DENNIS NR
      FISH AND MOLECULAR STUDY OF AUTOSOMAL SUPERNUMERARY MARKER CHROMOSOMES EXCLUDING THOSE DERIVED FROM CHROMOSOME-15 AND CHROMOSOME-22 - I - RESULTS OF 26 NEW CASES

      American journal of medical genetics
    49. CROLLA JA
      FISH AND MOLECULAR STUDIES OF AUTOSOMAL SUPERNUMERARY MARKER CHROMOSOMES EXCLUDING THOSE DERIVED FROM CHROMOSOME-15 - II - REVIEW OF THE LITERATURE

      American journal of medical genetics
    50. ENGELEN JJM; LOOTS WJG; ALBRECHTS JCM; PLOMP AS; VANDERMEER SB; VLES JSH; HAMERS GJH; GERAEDTS JPM
      CHARACTERIZATION OF A DE-NOVO UNBALANCED TRANSLOCATION T(14Q18Q) USING MICRODISSECTION AND FLUORESCENCE IN-SITU HYBRIDIZATION

      American journal of medical genetics
    51. Kaplan, J; Hukku, B
      Cell line characterization and authentication

      METHODS IN CELL BIOLOGY, VOL 57
    52. GHAFFARI SR; BOYD E; CONNOR JM; JONES AM; TOLMIE JL
      MOSAIC SUPERNUMERARY RING CHROMOSOME-19 IDENTIFIED BY COMPARATIVE GENOMIC HYBRIDIZATION

      Journal of Medical Genetics
    53. XU J; FONG CT; CEDRONE E; SULLIVAN J; WANG N
      PRENATAL IDENTIFICATION OF DE-NOVO MARKER CHROMOSOMES USING MICRO-FISH APPROACH

      Clinical genetics
    54. Wandall, A; Tranebjaerg, L; Tommerup, N
      A neocentromere on human chromosome 3 without detectable alpha-satellite DNA forms morphologically normal kinetochores

      CHROMOSOMA
    55. VERSCHRAEGENSPAE MR; QUACK B; ROUSSEAUX S; PISON H; MESSIAEN L; DEPAEPE A; LESPINASSE J
      APPLICATION OF FLUORESCENCE IN-SITU HYBRIDIZATION TO THE IDENTIFICATION OF DIFFERENT MARKER CHROMOSOMES

      Annales de genetique
    56. WANDSTRAT AE; LEANACOX J; JENKINS L; SCHWARTZ S
      MOLECULAR CYTOGENETIC EVIDENCE FOR A COMMON BREAKPOINT IN THE LARGESTINVERTED DUPLICATIONS OF CHROMOSOME-15

      American journal of human genetics
    57. DUSART D; CANCILLA MR; EARLE E; MAO JI; SAFFERY R; TAINTON KM; KALITSIS P; MARTYN J; BARRY AE; CHOO KHA
      A FUNCTIONAL NEO-CENTROMERE FORMED THROUGH ACTIVATION OF A LATENT HUMAN CENTROMERE AND CONSISTING OF NON-ALPHA-SATELLITE DNA

      Nature genetics
    58. GHAYEE HK; DINNEY CP; PATHAK S
      DO LYMPHOCYTES CONTAIN CHROMOSOMAL LESIONS THAT ARE ALSO STABLE MARKERS IN CANCER-CELLS - LYMPHOCYTE AND TUMOR-CELL KARYOTYPING IN A MELANOMA PATIENT

      International journal of oncology
    59. CALLEN DF; YIP MY; EYRE HJ
      RAPID DETECTION OF EUCHROMATIN BY ALU-PRINS - USE IN CLINICAL CYTOGENETICS

      Chromosome research
    60. SHERIDAN E; WILLIAMS J; CAINE A; MORGAN R; MASON G; MUELLER RF
      COUNSELING IMPLICATIONS OF CHROMOSOMAL-ABNORMALITIES OTHER THAN TRISOMY-21 DETECTED THROUGH A MATERNAL SERUM SCREENING-PROGRAM

      British journal of obstetrics and gynaecology
    61. LEVY B; GERSHIN IF; DESNICK RJ; BABU A; GELB BD; HIRSCHHORN K; COTTER PD
      CHARACTERIZATION OF A DE-NOVO UNBALANCED CHROMOSOME REARRANGEMENT BY COMPARATIVE GENOMIC HYBRIDIZATION AND FLUORESCENCE IN-SITU HYBRIDIZATION

      Cytogenetics and cell genetics
    62. KUMAR C; KLEYMAN SM; SAMONTE RV; VERMA RS
      MARKER CHROMOSOMES IN FETAL LOSS

      Human reproduction
    63. MAU UA; BACKERT IT; KAISER P; KIESEL L
      CHROMOSOMAL FINDINGS IN 150 COUPLES REFERRED FOR GENETIC-COUNSELING PRIOR TO INTRACYTOPLASMIC SPERM INJECTION

      Human reproduction
    64. SENGER G; CHUDOBA I; FRIEDRICH U; TOMMERUP N; CLAUSSEN U; BRONDUMNIELSEN K
      PRENATAL-DIAGNOSIS OF A HALF-CRYPTIC TRANSLOCATION USING CHROMOSOME MICRODISSECTION

      Prenatal diagnosis
    65. ATKIN NB
      CYTOGENETICS OF CARCINOMA OF THE CERVIX UTERI - A REVIEW

      Cancer genetics and cytogenetics
    66. VELAGALETI GVN; THARAPEL SA; MARTENS PR; THARAPEL AT
      RAPID IDENTIFICATION OF MARKER CHROMOSOMES USING PRIMED IN-SITU LABELING (PRINS)

      American journal of medical genetics
    67. VIERSBACH R; ENGELS H; SCHWANITZ G
      IDENTIFICATION OF SUPERNUMERARY DER(20) CHROMOSOMES BY FISH IN 3 PATIENTS

      American journal of medical genetics
    68. FAGAN K; EDWARDS M
      SUPERNUMERARY RING CHROMOSOME-17 IDENTIFIED BY FLUORESCENT IN-SITU HYBRIDIZATION

      American journal of medical genetics
    69. HENEGARIU O; KERNEK S; KEATING MA; PALMER CG; HEEREMA NA
      PCR AND FISH ANALYSIS OF A RING Y-CHROMOSOME

      American journal of medical genetics
    70. BETTIO D; RIZZI N; GIARDINO D; GURRIERI F; SILVESTRI G; GRUGNI G
      FISH CHARACTERIZATION OF SMALL SUPERNUMERARY MARKER CHROMOSOMES IN 2 PRADER-WILLI PATIENTS

      American journal of medical genetics
    71. MENNICKE K; DIERCKS P; SCHLIEKER H; BALSPRATSCH M; ALHASANI S; DIEDRICH K; SCHWINGER E
      MOLECULAR CYTOGENETIC DIAGNOSTICS IN SPERM

      International journal of andrology
    72. SOUZA ID; GOLLOP TR
      THE MEANING OF CHROMOSOME MOSAICISM IN CHORIONIC VILLUS SAMPLING - A REVIEW

      Brazilian journal of genetics
    73. MACKIEOGILVIE C; WADDLE K; MANDEVILLE J; SELLER MJ; DOCHERTY Z
      RAPID IDENTIFICATION OF MULTIPLE SUPERNUMERARY RING CHROMOSOMES WITH A NEW FISH TECHNIQUE

      Journal of Medical Genetics
    74. MANEA SR; GERSHIN IF; BABU A; WILLNER JP; DESNICK RJ; COTTER PD
      MOSAICISM FOR A SMALL SUPERNUMERARY RING X-CHROMOSOME IN A DYSMORPHIC, GROWTH-RETARDED MALE - MOS47,XXY 48,XXY,+R(X)/

      Clinical genetics
    75. FISHER AM; ALGAZALI L; PRAMATHAN T; QUAIFE R; COCKWELL AE; BARBER JCK; EARNSHAW WC; AXELMAN J; MIGEON BR; TYLERSMITH C
      CENTROMERIC INACTIVATION IN A DICENTRIC HUMAN Y-21 TRANSLOCATION CHROMOSOME

      Chromosoma
    76. ULMER R; PFEIFFER RA; WIEST E; GOELZ R; TRAUTMANN U
      MULTIPLE (UP TO 7) DIFFERENT ACCESSORY SMALL MARKER CHROMOSOMES - PRENATAL-DIAGNOSIS AND FOLLOW-UP

      Annales de genetique
    77. CHOO KHA
      CENTROMERE DNA DYNAMICS - LATENT CENTROMERES AND NEOCENTROMERE FORMATION

      American journal of human genetics
    78. STONE D; NING Y; GUAN XY; KAISERKUPFER M; WYNSHAWBORIS A; BIESECKER L
      CHARACTERIZATION OF FAMILIAL PARTIAL 10P TRISOMY BY CHROMOSOMAL MICRODISSECTION, FISH, AND MICROSATELLITE DOSAGE ANALYSIS

      Human genetics
    79. BUKVIC N; SUSCA F; GENTILE M; TANGARI E; IANNIRUBERTO A; GUANTI G
      AN UNUSUAL DICENTRIC Y-CHROMOSOME WITH A FUNCTIONAL CENTROMERE WITH NO DETECTABLE ALPHA-SATELLITE

      Human genetics
    80. ENGELEN JJM; ALBRECHTS JCM; LOOTS WJG; HOLLANDERSCROMBACH BHTM; HAMERS AJH; GERAEDTS JPM
      APPLICATION OF MICRO-FISH TO DELINEATE DELETIONS

      Cytogenetics and cell genetics
    81. MULLERNAVIA J; NEBEL A; OEHLER D; THEILE U; ZABEL B; SCHLEIERMACHER E
      MICRODISSECTION AND DOP-PCR-BASED REVERSE CHROMOSOME PAINTING AS A FAST AND RELIABLE STRATEGY IN THE ANALYSIS OF VARIOUS STRUCTURAL CHROMOSOME-ABNORMALITIES

      Prenatal diagnosis
    82. HSU LYF; YU MT; RICHKIND KE; VANDYKE DL; CRANDALL BF; SAXE DF; KHODR GS; MENNUTI M; STETTEN G; MILLER WA; PRIEST JH
      INCIDENCE AND SIGNIFICANCE OF CHROMOSOME MOSAICISM INVOLVING AN AUTOSOMAL STRUCTURAL ABNORMALITY DIAGNOSED PRENATALLY THROUGH AMNIOCENTESIS- A COLLABORATIVE STUDY

      Prenatal diagnosis
    83. VROLIJK H; SLOOS WCR; VANDERIJKE FM; MESKER WE; NETTEN H; YOUNG IT; RAAP AK; TANKE HJ
      AUTOMATION OF SPOT COUNTING IN INTERPHASE CYTOGENETICS USING BRIGHTFIELD MICROSCOPY

      Cytometry
    84. ABELIOVICH D; YEHUDA O; BENNERIAH S; KAPELUSHNIK Y; BENYEHUDA D
      DUP(10Q) LACKING ALPHA-SATELLITE DNA IN BONE-MARROW CELLS OF A PATIENT WITH ACUTE MYELOID-LEUKEMIA

      Cancer genetics and cytogenetics
    85. FETNI R; KRABCHI K; MESSIER PE; RICHER CL; LEMIEUX N
      CHARACTERIZATION BY FLUORESCENCE AND ELECTRON-MICROSCOPY IN-SITU HYBRIDIZATION OF A DOUBLE Y-ISOCHROMOSOME

      American journal of medical genetics
    86. COELHO KEFD; EGASHIRA M; KATO R; FUJIMOTO M; MATSUMOTO N; RERKAMNUAYCHOKE B; ABE K; HARADA N; OHASHI H; FUKUSHIMA Y; NIIKAWA N
      DIAGNOSIS OF 4 CHROMOSOME-ABNORMALITIES OF UNKNOWN ORIGIN BY CHROMOSOME MICRODISSECTION AND SUBSEQUENT REVERSE AND FORWARD PAINTING

      American journal of medical genetics
    87. VANDENENDEN A; VERSCHRAEGENSPAE MR; VANROY N; DECALUWE W; DEPRAETER C; SPELEMAN F
      MOSAIC TETRASOMY 15Q25-]QTER IN A NEWBORN-INFANT WITH MULTIPLE ANOMALIES

      American journal of medical genetics
    88. ESMER MD; CARNEVALE A; GOMEZ L; DELCASTILLO V; FRIAS S
      FLUORESCENCE IN-SITU HYBRIDIZATION IN 6 P ATIENTS WITH CHROMOSOME-18 STRUCTURAL-ABERRATIONS AND IN 7 PATIENTS WITH MARKER CHROMOSOMES

      Revista de Investigacion Clinica
    89. ENGELEN JJM; LOOTS WJG; ALBRECHTS JCM; MOTOH PCC; FRYNS JP; HAMERS AJH; GERAEDTS JPM
      DISCLOSURE OF 5 BREAKPOINTS IN A COMPLEX CHROMOSOME REARRANGEMENT BY MICRODISSECTION AND FISH

      Journal of Medical Genetics
    90. BLENNOW E; TILLBERG E
      SMALL EXTRA RING CHROMOSOME DERIVED FROM CHROMOSOME 10P - CLINICAL REPORT AND CHARACTERIZATION BY FISH

      Journal of Medical Genetics
    91. VANDERSMAGT JJ; GILTAY JC; DENEF JJEM; SLABBERS GHPR
      LARGE INV DUP(15) CHROMOSOME IN 2 GENERATIONS

      Journal of Medical Genetics
    92. HINDKJAER J; BRANDT CA; STROMKJAER H; KOCH J; KOLVRAA S; BOLUND L
      PRIMED IN-SITU LABELING (PRINS) AS A RATIONAL PROCEDURE FOR IDENTIFICATION OF MARKER CHROMOSOMES USING A PANEL OF PRIMERS DIFFERENTIALLY TAGGING THE HUMAN-CHROMOSOMES

      Clinical genetics
    93. AALFS CM; JACOBS ME; NIESTEOTTER MA; HENNEKAM RCM; HOOVERS JMN
      2 SUPERNUMERARY MARKER CHROMOSOMES, DERIVED FROM CHROMOSOME-6 AND CHROMOSOME-9, IN A BOY WITH MILD DEVELOPMENTAL DELAY

      Clinical genetics
    94. VANLANGEN IM; OTTER MA; ARONSON DC; OVERWEGPLANDSOEN WCG; HENNEKAM RCM; LESCHOT NJ; HOOVERS JMN
      SUPERNUMERARY RING CHROMOSOME-20 CHARACTERIZED BY FLUORESCENCE IN-SITU HYBRIDIZATION

      Clinical genetics
    95. HOGGE WA; SURTI U; KOCHMAR SJ; MOWERYRUSHTON P; CUMBIE K
      MOLECULAR CYTOGENETICS - AN ESSENTIAL COMPONENT OF MODERN PRENATAL-DIAGNOSIS

      American journal of obstetrics and gynecology
    96. KAPUSCINSKI J
      DAPI - A DNA-SPECIFIC FLUORESCENT-PROBE

      Biotechnic & histochemistry
    97. KOCOVA M; WITCHEL SF; NALESNIK M; LEE PA; DICKMAN PS; MACGILLIVRAY MH; REITER EO; TRUCCO G; TRUCCO M
      Y-CHROMOSOMAL SEQUENCES IDENTIFIED IN GONADAL TISSUE OF 2 45,X PATIENTS WITH TURNER-SYNDROME

      Endocrine pathology
    98. JAMES RS; TEMPLE IK; DENNIS NR; CROLLA JA
      A SEARCH FOR UNIPARENTAL DISOMY IN CARRIERS OF SUPERNUMERARY MARKER CHROMOSOMES

      European journal of human genetics
    99. KUO PL; WU RC; TZENG CC; LIN SJ; LIU SS; HUANG KE
      DETECTION OF Y-CHROMOSOMAL DNA WITH MARKER CHROMOSOMES IN TURNERS-SYNDROME

      Journal of the Formosan Medical Association
    100. TUMER Z; BERG A; MIKKELSEN M
      ANALYSIS OF A WHOLE-ARM TRANSLOCATION BETWEEN CHROMOSOME-18 AND CHROMOSOME-20 USING FLUORESCENCE IN-SITU HYBRIDIZATION - DETECTION OF A BREAK IN THE CENTROMERIC ALPHA-SATELLITE SEQUENCES

      Human genetics


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Documento generato il 08/08/20 alle ore 09:10:06