Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where authors phrase all words ' ROGAN PK' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 61 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Rogan, PK; Cazcarro, PM; Knoll, JHM
      Sequence-based design of single-copy genomic DNA probes for fluorescence in situ hybridization

      GENOME RESEARCH
    2. von Kodolitsch, Y; Nienaber, CA; Fliegner, M; Rogan, PK
      Splice-site mutations and atherosclerosis: mechanisms and prediction models

      ZEITSCHRIFT FUR KARDIOLOGIE
    3. Svojanovsky, SR; Schneider, TD; Rogan, PK
      Redundant designations of BRCA1 intron 11 splicing mutation; c. 4216-2A > G; IVS11-2A > G; L78833, 37698, A > G

      HUMAN MUTATION
    4. Mowery-Rushton, PA; Hanchett, JM; Zipf, WB; Rogan, PK; Surti, U
      Mosaicism in Prader-Willi syndrome - Reply

      AMERICAN JOURNAL OF MEDICAL GENETICS
    5. Vockley, J; Rogan, PK; Anderson, BD; Willard, J; Seelan, RS; Smith, DI; Liu, WG
      Exon skipping in IVD RNA processing in isovaleric acidemia caused by pointmutations in the coding region of the IVD gene

      AMERICAN JOURNAL OF HUMAN GENETICS
    6. Rogan, PK; Faux, BM; Schneider, TD
      Information analysis of human splice site mutations. (vol 12, pg 153, 1998)

      HUMAN MUTATION
    7. Rogan, PK; Sabol, DW; Punnett, HH
      Maternal uniparental disomy of chromosome 21 in a normal child

      AMERICAN JOURNAL OF MEDICAL GENETICS
    8. Martin, RA; Sabol, DW; Rogan, PK
      Maternal uniparental disomy of chromosome 14 confined to an interstitial segment (14q23-14q24.2)

      JOURNAL OF MEDICAL GENETICS
    9. von Kodolitsch, Y; Pyeritz, RE; Rogan, PK
      Splice-site mutations in atherosclerosis candidate genes - Relating individual information to phenotype

      CIRCULATION
    10. Amos-Landgraf, JM; Ji, YG; Gottlieb, W; Depinet, T; Wandstrat, AE; Cassidy, SB; Driscoll, DJ; Rogan, PK; Schwartz, S; Nicholls, RD
      Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints

      AMERICAN JOURNAL OF HUMAN GENETICS
    11. Ohta, T; Gray, TA; Rogan, PK; Buiting, K; Gabriel, JM; Saitoh, S; Muralidhar, B; Bilienska, B; Krajewska-Walasek, M; Driscoll, DJ; Horsthemke, B; Butler, MG; Nicholls, RD
      Imprinting-mutation mechanisms in Prader-Willi syndrome

      AMERICAN JOURNAL OF HUMAN GENETICS
    12. ONEIL JP; ROGAN PK; CARIELLO N; NICKLAS JA
      MUTATIONS THAT ALTER RNA SPLICING OF THE HUMAN HPRT GENE - A REVIEW OF THE SPECTRUM

      Mutation research. Reviews in mutation research
    13. ROGAN PK; FAUX BM; SCHNEIDER TD
      INFORMATION ANALYSIS OF HUMAN SPLICE-SITE MUTATIONS

      Human mutation
    14. TOOLEY PW; SALVO JJ; SCHNEIDER TD; ROGAN PK
      PHYLOGENETIC INFERENCE BASED ON INFORMATION THEORY-BASED PCR AMPLIFICATION

      Journal of phytopathology
    15. ALLIKMETS R; WASSERMAN WW; HUTCHINSON A; SMALLWOOD P; NATHANS J; ROGAN PK; SCHNEIDER TD; DEAN M
      ORGANIZATION OF THE ABCR GENE - ANALYSIS OF PROMOTER AND SPLICE JUNCTION SEQUENCES

      Gene
    16. GOCKE CD; BENKO FA; ROGAN PK
      TRANSMISSION OF MITOCHONDRIAL-DNA HETEROPLASMY IN NORMAL PEDIGREES

      Human genetics
    17. Rogan, PK; Seip, JR; White, LM; Wenger, SL; Steele, MW; Sperling, MA; Menon, R; Knoll, JHM
      Relaxation of imprinting in Prader-Willi syndrome

      HUMAN GENETICS
    18. ROGAN PK; SEIP JR; KNOLL JHM; WHITE LM; WENGER SL; STEELE MW; SPERLING MA; APARICIO L; MENON R
      RELAXATION OF IMPRINTING IN PATIENTS WITH PRADER-WILLI-SYNDROME

      American journal of medical genetics
    19. OHTA T; SAITOH S; BUITING K; GABRIEL JM; SCHWARTZ S; CASSIDY SB; ROGAN PK; GLENN CC; DRISCOLL DJ; HORSTHEMKE B; NICHOLLS RD
      IMPRINTING MUTATIONS IN PRADER-WILLI (AND ANGELMAN) SYNDROME EXEMPLIFY A NEW GENETIC MECHANISM

      American journal of medical genetics
    20. BUTLER MG; ROGAN PK
      ATYPICAL CLINICAL FINDINGS IN PRADER-WILLI-SYNDROME PATIENTS

      American journal of medical genetics
    21. BUTLER MG; HEDGES LK; ROGAN PK; SEIP JR; CASSIDY SB; MOESCHLER JB
      KLINEFELTER-SYNDROME AND TRISOMY-X-SYNDROME IN PATIENTS WITH PRADER-WILLI-SYNDROME AND UNIPARENTAL MATERNAL DISOMY OF CHROMOSOME-15 - A COINCIDENCE

      American journal of medical genetics
    22. SAITOH S; BUITING K; CASSIDY SB; CONROY JM; DRISCOLL DJ; GABRIEL JM; GILLESSENKAESBACH G; GLENN CC; GREENSWAG LR; HORSTHEMKE B; KONDO I; KUWAJIMA K; NIIKAWA N; ROGAN PK; SCHWARTZ S; SEIP J; WILLIAMS CA; NICHOLLS RD
      CLINICAL SPECTRUM AND MOLECULAR DIAGNOSIS OF ANGELMAN AND PRADER-WILLI-SYNDROME PATIENTS WITH AN IMPRINTING MUTATION

      American journal of medical genetics
    23. ROGAN PK; SCHNEIDER TD; FAUX B; WIJNEN J; RADICE P; BABA S; SCOTT R; VIEL A; GENUARDI M; KHAN PM; FODDE R
      INFORMATION THEORY-BASED ANALYSIS OF SPLICE JUNCTION MUTATIONS IN HEREDITARY NONPOLYPOSIS COLON-CANCER (HNPCC)

      American journal of human genetics
    24. BELCHIS DA; MEECE CA; BENKO FA; ROGAN PK; WILLIAMS RA; GOCKE CD
      LOSS OF HETEROZYGOSITY AND MICROSATELLITE INSTABILITY AT THE RETINOBLASTOMA LOCUS IN OSTEOSARCOMAS

      Diagnostic molecular pathology
    25. FLOROS J; DIANGELO S; KOPTIDES M; KARINCH AM; ROGAN PK; NIELSEN H; SPRAGG RG; WATTERBERG K; DEITER G
      HUMAN SP-A LOCUS - ALLELE FREQUENCIES AND LINKAGE DISEQUILIBRIUM BETWEEN THE 2 SURFACTANT PROTEIN-A GENES

      American journal of respiratory cell and molecular biology
    26. VELETZA SV; ROGAN PK; TENHAVE T; OLOWE SA; FLOROS J
      RACIAL-DIFFERENCES IN ALLELIC DISTRIBUTION AT THE HUMAN PULMONARY SURFACTANT PROTEIN-B GENE LOCUS (SP-B)

      Experimental lung research
    27. VGONTZAS AN; KALES A; SEIP J; MASCARI MJ; BIXLER EO; MYERS DC; VELABUENO A; ROGAN PK
      RELATIONSHIP OF SLEEP ABNORMALITIES TO PATIENT GENOTYPES IN PRADER-WILLI-SYNDROME

      American journal of medical genetics
    28. MOWERYRUSHTON PA; HANCHETT JM; ZIPF WB; ROGAN PK; SURTI U
      IDENTIFICATION OF MOSAICISM IN PRADER-WILLI-SYNDROME USING FLUORESCENT IN-SITU HYBRIDIZATION

      American journal of medical genetics
    29. ROGAN PK; MASCARI MJ; LADDA RL; WOODAGE T; TRENT RJ; SMITH A; LAI LW; ERICKSON RP; CASSIDY SB; PETERSEN MB; MIKKELSEN M; DRISCOLL DJ; NICHOLLS RD; BUTLER MG
      COINHERITANCE OF OTHER CHROMOSOME-15 ABNORMALITIES WITH PRADER-WILLI-SYNDROME - GENETIC RISK-ESTIMATION AND MAPPING

      American journal of medical genetics
    30. ROGAN PK; SEIP JR; DRISCOLL DJ; PAPENHAUSEN PR; JOHNSON VP; RASKIN S; WOODWARD AL; BUTLER MG
      DISTINCT 15Q GENOTYPES IN RUSSELL-SILVER AND RING-15 SYNDROMES

      American journal of medical genetics
    31. SAITOH S; BUITING K; ROGAN PK; BUXTON JL; DRISCOLL DJ; ARNEMANN J; KONIG R; MALCOLM S; HORSTHEMKE B; NICHOLLS RD
      MINIMAL DEFINITION OF THE IMPRINTING CENTER AND FIXATION OF A CHROMOSOME 15Q11-Q13 EPIGENOTYPE BY IMPRINTING MUTATIONS

      Proceedings of the National Academy of Sciences of the United Statesof America
    32. WHITE LM; ROGAN PK; NICHOLLS RD; WU BL; KORF B; KNOLL JHM
      ALLELE-SPECIFIC REPLICATION OF 15Q11-Q13 LOCI - A DIAGNOSTIC-TEST FORDETECTION OF UNIPARENTAL DISOMY

      American journal of human genetics
    33. CONSEVAGE MW; SEIP JR; BELCHIS DA; DAVIS AT; BAYLEN BG; ROGAN PK
      ASSOCIATION OF A MOSAIC CHROMOSOMAL 22Q11 DELETION WITH HYPOPLASTIC LEFT-HEART SYNDROME

      The American journal of cardiology
    34. ROGAN PK; SCHNEIDER TD
      USING INFORMATION-CONTENT AND BASE FREQUENCIES TO DISTINGUISH MUTATIONS FROM GENETIC POLYMORPHISMS IN SPLICE JUNCTION RECOGNITION SITES

      Human mutation
    35. KAUFFMAN EJ; GESTL EE; KIM DJ; WALKER C; HITE JM; YAN G; ROGAN PK; JOHNSON SL; CHENG KC
      MICROSATELLITE-CENTROMERE MAPPING IN THE ZEBRAFISH (DANIO-RERIO)

      Genomics
    36. ROGAN PK; BLOUIN JL; CLOSE P; SEIP JR; GANNUTZ LS; LADDA RL; ANTONARAKIS SE
      DUPLICATION AND LOSS OF CHROMOSOME-21 IN 2 CHILDREN WITH DOWN-SYNDROME AND ACUTE-LEUKEMIA

      Cytogenetics and cell genetics
    37. ORR GA; ROGAN PK
      DEVELOPMENT OF A DIRECTORY OF GENETIC PROBES AS A SHARED INSTITUTIONAL RESOURCE

      Computer methods and programs in biomedicine
    38. HESS EJ; ROGAN PK; DOMOTO M; TINKER DE; LADDA RL; RAMER JC
      ABSENCE OF LINKAGE OF APPARENTLY SINGLE-GENE MEDIATED ADHD WITH THE HUMAN SYNTENIC REGION OF THE MOUSE MUTANT COLOBOMA

      American journal of medical genetics
    39. ROGAN PK; CLOSE P; BLOUIN JL; SEIP JR; GANNUTZ L; LADDA RL; ANTONARAKIS SE
      DUPLICATION AND LOSS OF CHROMOSOME-21 IN 2 CHILDREN WITH DOWN-SYNDROME AND ACUTE-LEUKEMIA

      American journal of medical genetics
    40. BELCHIS DA; MEECE CA; ROGAN PK; WILLIAMS R; GOCKE CD
      DETECTION OR MOLECULAR-CHANGES AT THE RETINOBLASTOMA LOCUS IN OSTEOSARCOMAS BY THE POLYMERASE CHAIN-REACTION

      Laboratory investigation
    41. KNOLL JHM; ROGAN PK; NICHOLLS RD; WU B; KORF B; WHITE L
      ALLELE-SPECIFIC REPLICATION OF 15Q11Q13 LOCI - A DIAGNOSTIC-TEST FOR DETECTION OF UNIPARENTAL DISOMY

      American journal of human genetics
    42. SAITOH S; ROGAN PK; BUITING K; SCHWARTZ S; CASSIDY SB; GLENN CC; DRISCOLL DJ; HORSTHEMKE B; NICHOLLS RD
      MINIMAL DEFINITION OF THE IMPRINTING CENTER AND FIXATION OF A CHROMOSOME 15Q11-Q13 EPIGENOTYPE BY IMPRINTING MUTATIONS

      American journal of human genetics
    43. GOCKE CD; SIMMONS Z; BENKO FA; TOWFIGHI J; ROGAN PK
      CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA (CPEO) AND LIMB-GIRDLE DYSTROPHY IN 2 MEMBERS OF A FAMILY WITH DIFFERENT MITOCHONDRIAL-DNA (MTDNA) DELETIONS

      American journal of human genetics
    44. CONSEVAGE MW; SALADA GC; BAYLEN BG; LADDA RL; ROGAN PK
      A NEW MISSENSE MUTATION, ARG719GLN, IN THE BETA-CARDIAC HEAVY-CHAIN MYOSIN GENE OF PATIENTS WITH FAMILIAL HYPERTROPHIC CARDIOMYOPATHY (VOL 3, PG 1025, 1994)

      Human molecular genetics
    45. CONSEVAGE MW; SALADA GC; BAYLEN BG; LADDA RL; ROGAN PK
      A NEW MISSENSE MUTATION, ARG719GLN, IN THE BETA-CARDIAC HEAVY-CHAIN MYOSIN GENE OF PATIENTS WITH FAMILIAL HYPERTROPHIC CARDIOMYOPATHY

      Human molecular genetics
    46. GABRIEL J; GOTTLIEB W; GARCIA A; ROGAN PK; SAITOH S; NICHOLLS RD
      A COMMON INSERTION DELETION POLYMORPHISM IN THE PRADER-WILLI-SYNDROMEMINIMAL CRITICAL REGION/

      Human molecular genetics
    47. BUTLER MG; WOODWARD AL; DRISCOLL DJ; PAPENHAUSEN PR; JOHNSON VP; RASKIN S; ROGAN PK
      MOLECULAR-GENETIC ANALYSIS OF 15Q-]QTER MARKERS IN PATIENTS WITH RING-15 AND RUSSELL-SILVER-SYNDROMES

      Cytogenetics and cell genetics
    48. ROGAN PK; MASCARI MJ; LADDA RL; WOODAGE T; TRENT RJ; SMITH A; LAI LW; ERICKSON RP; CASSIDY SB; PETERSEN MB; MIKKELSEN M; DRISCOLL DJ; NICHOLLS RD
      PERTURBED RECOMBINATION OF CHROMOSOME-15 IN PRADER-WILLI PATIENTS WITH MATERNAL DISOMY

      Cytogenetics and cell genetics
    49. WOODAGE T; PRASAD M; DIXON JW; SELBY RE; ROMAIN DR; COLUMBANOGREEN LM; GRAHAM D; SEIP JR; ROGAN PK; SMITH A; TRENT RJ
      LOCALIZATION OF THE BLOOM-SYNDROME GONE BY HOMOZYGOSITY MAPPING IN A PATIENT WITH MATERNAL UNIPARENTAL DISOMY OF CHROMOSOME-15

      Cytogenetics and cell genetics
    50. CONSEVAGE MW; SALADA GC; BAYLEN BG; LADDA RL; ROGAN PK
      A NEW MISSENSE MUTATION IN EXON-19 OF THE BETA-CARDIAC HEAVY-CHAIN MYOSIN GENE (MHC) IN A FAMILY WITH FAMILIAL HYPERTROPHIC CARDIOMYOPATHY - ARG719GLN

      Pediatric research
    51. KRIZKOVA L; SAKTHIVEL R; OLOWE SA; ROGAN PK; FLOROS J
      HUMAN SP-A - GENOTYPE AND SINGLE-STRAND CONFORMATION POLYMORPHISM ANALYSIS

      The American journal of physiology
    52. WOODAGE T; PRASAD M; DIXON JW; SELBY RE; ROMAIN DR; COLUMBANOGREEN LM; GRAHAM D; ROGAN PK; SEIP JR; SMITH A; TRENT RJ
      BLOOM-SYNDROME AND MATERNAL UNIPARENTAL DISOMY FOR CHROMOSOME-15

      American journal of human genetics
    53. LADDA RL; ZONANA J; RAMER JC; MASCARI MJ; ROGAN PK
      CONGENITAL CONTRACTURES, ECTODERMAL DYSPLASIA, CLEFT-LIP PALATE, AND DEVELOPMENTAL IMPAIRMENT - A DISTINCT SYNDROME

      American journal of medical genetics
    54. MOWREY PN; CHORNEY MJ; VENDITTI CP; LATIF F; MODI WS; LERMAN MI; ZBAR B; ROBINS DB; ROGAN PK; LADDA RL
      CLINICAL AND MOLECULAR ANALYSES OF DELETION 3P25-PTER SYNDROME

      American journal of medical genetics
    55. MASCARI MJ; LADDA RL; WOODAGE T; TRENT RJ; LAI LW; ERICKSON RP; CASSIDY SB; PETERSEN MB; MIKKELSEN M; DRISCOLL DJ; NICHOLLS RD; ROGAN PK
      PERTURBED RECOMBINATION OF CHROMOSOME-15 IN PRADER-WILLI PATIENTS WITH MATERNAL DISOMY

      American journal of human genetics
    56. GOTTLIEB W; ROGAN PK; DRISCOLL DJ; NICHOLLS RD
      ANALYSIS OF CHROMOSOME-BREAKAGE MECHANISMS IN PRADER-WILLI AND ANGELMAN SYNDROMES

      American journal of human genetics
    57. FLOROS J; RISHI A; VELETZA SV; ROGAN PK
      CONCERTED AND INDEPENDENT GENETIC EVENTS IN THE 3'UNTRANSLATED REGIONOF THE HUMAN SURFACTANT PROTEIN-A GENES

      American journal of human genetics
    58. GUIDA L; ROGAN PK; CHAKRAVARTI A; SCHWARTZ S; NICHOLLS RD
      ISOLATION OF (CA)N REPEATS AND CHARACTERIZATION OF THE PERICENTROMERIC REGION OF CHROMOSOME-15Q

      American journal of human genetics
    59. BUTLER MG; DRISCOLL DJ; PAPENHAUSEN PR; JOHNSON VP; ROGAN PK
      ANALYSIS OF 15Q25-]QTER MARKERS IN PATIENTS WITH RING-15 AND RUSSELL-SILVER SYNDROMES

      American journal of human genetics
    60. ROGAN PK; LICHTY TR; LADDA RL; MASCARI MJ; STEELE MW; WENGER SL; MALCOLM S; DRISCOLL DJ; NICHOLLS RD
      UNIPARENTAL DISOMY IN ANGELMAN SYNDROME - A CONSEQUENCE OF PATERNAL MEIOTIC NONDISJUNCTION

      American journal of human genetics
    61. PHILLIPS RL; ROGAN PK; CULIAT CT; STUBBS L; RINCHIK EM; GOTTLIEB W; NICHOLLS RD
      A YAC CONTIG SPANNING 4 GENES IN DISTAL HUMAN CHROMOSOME-15Q11-Q13, MAPPING OF THE HUMAN GABRG3 GENE, AND EFFECT OF HOMOZYGOUS DELETION OF 3 GABA-A RECEPTOR GENES IN MOUSE

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 29/10/20 alle ore 18:14:07