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    1. Nicholls, RD; Knepper, JL
      Genome organization, function and imprinting in Prader-Willi and Angelman syndromes

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    2. Meguro, M; Kashiwagi, A; Mitsuya, K; Nakao, M; Kondo, I; Saitoh, S; Oshimura, M
      A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome

      NATURE GENETICS
    3. El-Maarri, O; Buiting, K; Peery, EG; Kroisel, PM; Balaban, B; Wagner, K; Urman, B; Heyd, J; Lich, C; Brannan, CI; Walter, J; Horsthemke, B
      Maternal methylation imprints on human chromosome 15 are established during or after fertilization

      NATURE GENETICS
    4. Runte, M; Farber, C; Lich, C; Zeschnigk, M; Buchholz, T; Smith, A; Van Maldergem, L; Burger, J; Muscatelli, F; Gillessen-Kaesbach, G; Horsthemke, B; Buiting, K
      Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15

      EUROPEAN JOURNAL OF HUMAN GENETICS
    5. Fulmer-Smentek, SB; Francke, U
      Association of acetylated histones with paternally expressed genes in the Prader-Willi deletion region

      HUMAN MOLECULAR GENETICS
    6. Meguro, M; Mitsuya, K; Nomura, N; Kohda, M; Kashiwagi, A; Nishigaki, R; Yoshioka, H; Nakao, M; Oishi, M; Oshimura, M
      Large-scale evaluation of imprinting status in the Prader-Willi syndrome region: an imprinted direct repeat cluster resembling small nucleolar RNA genes

      HUMAN MOLECULAR GENETICS
    7. Chai, JH; Locke, DP; Ohta, T; Greally, JM; Nicholls, RD
      Retrotransposed genes such as Frat3 in the mouse Chromosome 7C Prader-Willi syndrome region acquire the imprinted status of their insertion site

      MAMMALIAN GENOME
    8. Chamberlain, SJ; Brannan, CI
      The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a

      GENOMICS
    9. Sleutels, F; Barlow, DP
      Investigation of elements sufficient to imprint the mouse air promoter

      MOLECULAR AND CELLULAR BIOLOGY
    10. Rakyan, VK; Preis, J; Morgan, HD; Whitelaw, E
      The marks, mechanisms and memory of epigenetic states in mammals

      BIOCHEMICAL JOURNAL
    11. Luo, RZ; Peng, HQ; Xu, FJ; Bao, JJ; Pang, Y; Pershad, R; Issa, JPJ; Liao, WSL; Bast, RC; Yu, YH
      Genomic structure and promoter characterization of an imprinted tumor suppressor gene ARHI

      BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION
    12. Manning, M; Lissens, W; Liebaers, I; Van Steirteghem, A; Weidner, W
      Imprinting analysis in spermatozoa prepared for intracytoplasmic sperm injection (ICSI)

      INTERNATIONAL JOURNAL OF ANDROLOGY
    13. Manning, M; Lissens, W; Weidner, W; Liebaers, I
      DNA methylation analysis in immature testicular sperm cells at different developmental stages

      UROLOGIA INTERNATIONALIS
    14. El Kharroubi, A; Piras, G; Stewart, CL
      DNA demethylation reactivates a subset of imprinted genes in uniparental mouse embryonic fibroblasts

      JOURNAL OF BIOLOGICAL CHEMISTRY
    15. Xin, ZH; Allis, CD; Wagstaff, J
      Parent-specific complementary patterns of histone H3 lysine 9 and H3 lysine 4 methylation at the Prader-Willi syndrome imprinting center

      AMERICAN JOURNAL OF HUMAN GENETICS
    16. Buiting, K; Barnicoat, A; Lich, C; Pembrey, M; Malcolm, S; Horsthemke, B
      Disruption of the bipartite imprinting center in a family with Angelman syndrome

      AMERICAN JOURNAL OF HUMAN GENETICS
    17. Fridman, C; Koiffmann, CP
      Genomic imprinting: genetic mechanisms and phenotypic consequences in Prader-Willi and Angelman syndromes

      GENETICS AND MOLECULAR BIOLOGY
    18. Manning, M; Lissens, W; Bonduelle, M; Camus, M; De Rijcke, M; Liebaers, I; Van Steirteghem, A
      Study of DNA-methylation patterns at chromosome 15q11-q13 in children bornafter ICSI reveals no imprinting defects

      MOLECULAR HUMAN REPRODUCTION
    19. Fridman, C; Varela, MC; Kok, F; Setian, N; Koiffmann, CP
      Prader-Willi syndrome: Genetic tests and clinical findings

      GENETIC TESTING
    20. Onyango, P; Miller, W; Lehoczky, J; Leung, CT; Birren, B; Wheelan, S; Dewar, K; Feinberg, AP
      Sequence and comparative analysis of the mouse 1-megabase region orthologous to the human 11p15 imprinted domain

      GENOME RESEARCH
    21. Shemer, R; Hershko, AY; Perk, J; Mostoslavsky, R; Tsuberi, B; Cedar, H; Buiting, K; Razin, A
      The imprinting box of the Prader-Willi/Angelman syndrome domain

      NATURE GENETICS
    22. Butler, MG; Thompson, T
      Prader-Willi syndrome: Clinical and genetic findings

      ENDOCRINOLOGIST
    23. Ben-Porath, I; Cedar, H
      Imprinting: focusing on the center

      CURRENT OPINION IN GENETICS & DEVELOPMENT
    24. Farber, C; Gross, S; Neesen, J; Buiting, K; Horsthemke, B
      Identification of a testis-specific gene (C15orf2) in the Prader-Willi syndrome region on chromosome 15

      GENOMICS
    25. Glenn, CC; Deng, G; Michaelis, RC; Tarleton, J; Phelan, MC; Surh, L; Yang, TP; Driscoll, DJ
      DNA methylation analysis with respect to prenatal diagnosis of the Angelman and Prader-Willi syndromes and imprinting

      PRENATAL DIAGNOSIS
    26. Fridman, C; Varela, MC; Kok, F; Diament, A; Koiffmann, CP
      Paternal UPD15: Further genetic and clinical studies in four Angelman syndrome patients

      AMERICAN JOURNAL OF MEDICAL GENETICS
    27. Lee, JT
      Disruption of imprinted X inactivation by parent-of-origin effects at Tsix

      CELL
    28. Nemtsova, MV
      Genomic imprinting and human hereditary disorders

      MOLECULAR BIOLOGY
    29. McEntagart, ME; Webb, T; Hardy, C; King, MD
      Familial Prader-Willi syndrome: Case report and a literature review

      CLINICAL GENETICS
    30. Sunahara, S; Nakamura, K; Nakao, K; Gondo, Y; Nagata, Y; Katsuki, M
      The oocyte-specific methylated region of the U2afbp-rs/U2af1-rs1 gene is dispensable for its imprinted methylation

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    31. de los Santos, T; Schweizer, J; Rees, CA; Francke, U
      Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which is highly expressed in brain

      AMERICAN JOURNAL OF HUMAN GENETICS
    32. Pfeifer, K
      Mechanisms of genomic imprinting

      AMERICAN JOURNAL OF HUMAN GENETICS
    33. Lossie, AC; Driscoll, DJ
      Transmission of Angelman syndrome by an affected mother

      GENETICS IN MEDICINE
    34. Jong, MTC; Gray, TA; Ji, YG; Glenn, CC; Saitoh, S; Driscoll, DJ; Nicholls, RD
      A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region

      HUMAN MOLECULAR GENETICS
    35. Jong, MTC; Carey, AH; Caldwell, KA; Lau, MH; Handel, MA; Driscoll, DJ; Stewart, CL; Rinchik, EM; Nicholls, RD
      Imprinting of a RING zinc-finger encoding gene in the mouse chromosome region homologous to the Prader-Willi syndrome genetic region

      HUMAN MOLECULAR GENETICS
    36. Boccaccio, I; Glatt-Deeley, H; Watrin, F; Roeckel, N; Lalande, M; Muscatelli, F
      The human MAGEL2 gene and its mouse homologue are paternally expressed andmapped to the Prader-Willi region

      HUMAN MOLECULAR GENETICS
    37. Mann, MRW; Bautolomei, MS
      Towards a molecular understanding of Prader-Willi and Angelman syndromes

      HUMAN MOLECULAR GENETICS
    38. Brannan, CI; Bartolomei, MS
      Mechanisms of genomic imprinting

      CURRENT OPINION IN GENETICS & DEVELOPMENT
    39. Kato, Y; Rideout, WM; Hilton, K; Barton, SC; Tsunoda, Y; Surani, MA
      Developmental potential of mouse primordial germ cells

      DEVELOPMENT
    40. Tanaka, M; Puchyr, M; Gertsenstein, M; Harpal, K; Jaenisch, R; Rossant, J; Nagy, A
      Parental origin-specific expression of Mash2 is established at the time ofimplantation with its imprinting mechanism highly resistant to genome-widedemethylation

      MECHANISMS OF DEVELOPMENT
    41. Hershko, A; Razin, A; Shemer, R
      Imprinted methylation and its effect on expression of the mouse Zfp127 gene

      GENE
    42. Tilghman, SM
      The sins of the fathers and mothers: Genomic imprinting in mammalian development

      CELL
    43. Greally, JM; Gray, TA; Gabriel, JM; Song, LQ; Zemel, S; Nicholls, RD
      Conserved characteristics of heterochromatin-forming DNA at the 15q11-q13 imprinting center

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    44. Schmidt, JV; Levorse, JM; Tilghman, SM
      Enhancer competition between H19 and Igf2 does not mediate their imprinting

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    45. Gray, TA; Saitoh, S; Nicholls, RD
      An imprinted, mammalian bicistronic transcript encodes two independent proteins

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    46. Kanduri, C; Pfeifer, S; Li, YM; Ohlsson, R
      Genes without protein products: Is H19 the norm or the exception?

      CURRENT SCIENCE
    47. Buiting, K; Dittrich, B; Dworniczak, B; Lerer, I; Abeliovich, D; Cottrell, S; Temple, IK; Harvey, JF; Lich, C; Gross, S; Horsthemke, B
      A 28-kb deletion spanning D15S63 (PW71) in five families: A rare neutral variant?

      AMERICAN JOURNAL OF HUMAN GENETICS
    48. Ohta, T; Buiting, K; Kokkonen, H; McCandless, S; Heeger, S; Leisti, H; Driscoll, DJ; Cassidy, SB; Horsthemke, B; Nicholls, RD
      Molecular mechanism of Angelman syndrome in two large families involves animprinting mutation

      AMERICAN JOURNAL OF HUMAN GENETICS
    49. 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
    50. HOLLAND AJ
      UNDERSTANDING THE EATING DISORDER AFFECTING PEOPLE WITH PRADER-WILLI-SYNDROME

      JARID. Journal of applied research in intellectual disabilities
    51. SCHUMACHER A; BUITING K; ZESCHNIGK M; DOERFLER W; HORSTHEMKE B
      METHYLATION ANALYSIS OF THE PWS AS REGION DOES NOT SUPPORT AN ENHANCER-COMPETITION MODEL/

      Nature genetics
    52. YANG T; ADAMSON TE; RESNICK JL; LEFF S; WEVRICK R; FRANCKE U; JENKINS NA; COPELAND NG; BRANNAN CI
      A MOUSE MODEL FOR PRADER-WILLI-SYNDROME IMPRINTING-CENTER MUTATIONS

      Nature genetics
    53. TILGHMAN SM; CASPARY T; INGRAM RS
      COMPETITIVE EDGE AT THE IMPRINTED PRADER-WILLI ANGELMAN REGION/

      Nature genetics
    54. CONSTANCIA M; PICKARD B; KELSEY G; REIK W
      IMPRINTING MECHANISMS

      PCR methods and applications
    55. CHRISTIAN SL; BHATT NK; MARTIN SZ; SUTCLIFFE JS; KUBOTA T; HUANG B; MUTIRANGURA A; CHINAULT AC; BEAUDET AL; LEDBETTER DH
      INTEGRATED YAC CONTIG MAP OF THE PRADER-WILLI ANGELMAN-REGION ON CHROMOSOME-15Q11-Q13 WITH AVERAGE STS SPACING OF 35-KB/

      PCR methods and applications
    56. KELSEY G; REIK W
      ANALYSIS AND IDENTIFICATION OF IMPRINTED GENES

      Methods
    57. JIANG YH; TSAI TF; BRESSLER J; BEAUDET AL
      IMPRINTING IN ANGELMAN AND PRADER-WILLI SYNDROMES

      Current opinion in genetics & development
    58. REIK W; WALTER J
      IMPRINTING MECHANISMS IN MAMMALS

      Current opinion in genetics & development
    59. DUPONT JM; CUISSET L
      GENETIC-BASIS OF PRADER-WILLI AND ANGELMA N-SYNDROMES - IMPLICATIONS FOR DIAGNOSTIC TESTING

      Archives de pediatrie
    60. DUVILLE B; BUCCHINI D; TANG TW; JAMI J; PALDI A
      IMPRINTING AT THE MOUSE INS2 LOCUS - EVIDENCE FOR CIS-ALLELIC AND TRANS-ALLELIC INTERACTIONS

      Genomics
    61. 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
    62. BUITING K; GROSS S; JI Y; SENGER G; NICHOLLS RD; HORSTHEMKE B
      EXPRESSED COPIES OF THE MN7 (D15F37) GENE FAMILY MAP CLOSE TO THE COMMON DELETION BREAKPOINTS IN THE PRADER-WILLI ANGELMAN-SYNDROMES/

      Cytogenetics and cell genetics
    63. CASPARY T; CLEARY MA; BAKER CC; GUAN XJ; TILGHMAN SM
      MULTIPLE MECHANISMS REGULATE IMPRINTING OF THE MOUSE DISTAL CHROMOSOME-7 GENE-CLUSTER

      Molecular and cellular biology
    64. NICHOLLS RD; SAITOH S; HORSTHEMKE B
      IMPRINTING IN PRADER-WILLI AND ANGELMAN-SYNDROMES

      Trends in genetics
    65. MALZAC P; MONCLA A; PEDEILLIER K; VAN CV; GIRARDOT L; VOELCKEL MA
      ATYPICAL MOLECULAR FINDINGS IDENTIFY LIMITS OF TECHNICAL SCREENING-TESTS FOR PRADER-WILLI AND ANGELMAN SYNDROME DIAGNOSES

      American journal of medical genetics
    66. LASALLE JM; RITCHIE RJ; GLATT H; LALANDE M
      CLONAL HETEROGENEITY AT ALLELIC METHYLATION SITES DIAGNOSTIC FOR PRADER-WILLI-AND-ANGELMAN-SYNDROMES

      Proceedings of the National Academy of Sciences of the United Statesof America
    67. LYKO F; BUITING K; HORSTHEMKE B; PARO R
      IDENTIFICATION OF A SILENCING ELEMENT IN THE HUMAN 15Q11-Q13 IMPRINTING CENTER BY USING TRANSGENIC DROSOPHILA

      Proceedings of the National Academy of Sciences of the United Statesof America
    68. Gabriel, JM; Higgins, MJ; Gebuhr, TC; Shows, TB; Saitoh, S; Nicholls, RD
      A model system to study genomic imprinting of human genes

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    69. CASSIDY SB; SCHWARTZ S
      PRADER-WILLI AND ANGELMAN SYNDROMES - DISORDERS OF GENOMIC IMPRINTING

      Medicine
    70. CHOTAI KA; PAYNE SJ
      A RAPID, PCR BASED TEST FOR DIFFERENTIAL MOLECULAR DIAGNOSIS OF PRADER-WILLI AND ANGELMAN-SYNDROMES

      Journal of Medical Genetics
    71. BUITING K; DITTRICH B; GROSS S; LICH C; FARBER C; BUCHHOLZ T; SMITH E; REIS A; BURGER J; NOTHEN MM; BARTHWITTE U; JANSSEN B; ABELIOVICH D; LERER I; VANDENOUWELAND AMW; HALLEY DJJ; SCHRANDERSTUMPEL C; SMEETS H; MEINECKE P; MALCOLM S; GARDNER A; LALANDE M; NICHOLLS RD; FRIEND K; SCHULZE A; MATTHIJS G; KOKKONEN H; HILBERT P; VANMALDERGEM L; GLOVER G; CARBONELL P; WILLEMS P; GILLESSENKAESBACH G; HORSTHEMKE B
      SPORADIC IMPRINTING DEFECTS IN PRADER-WILLI-SYNDROME AND ANGELMAN-SYNDROME - IMPLICATIONS FOR IMPRINT-SWITCH MODELS, GENETIC-COUNSELING, AND PRENATAL-DIAGNOSIS

      American journal of human genetics
    72. 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
    73. GLENN CC; DRISCOLL DJ; YANG TP; NICHOLLS RD
      GENOMIC IMPRINTING - POTENTIAL FUNCTION AND MECHANISMS REVEALED BY THE PRADER-WILLI AND ANGELMAN SYNDROMES

      Molecular human reproduction
    74. JAY P; ROUGEULLE C; MASSACRIER A; MONCLA A; MATTEI MG; MALZAC P; ROECKEL N; TAVIAUX S; LEFRANC JLB; CAU P; BERTA P; LALANDE M; MUSCATELLI F
      THE HUMAN NECDIN GENE, NDN, IS MATERNALLY IMPRINTED AND LOCATED IN THE PRADER-WILLI-SYNDROME CHROMOSOMAL REGION

      Nature genetics
    75. MATSUURA T; SUTCLIFFE JS; FANG P; GALJAARD RJ; JIANG YH; BENTON CS; ROMMENS JM; BEAUDET AL
      DE-NOVO TRUNCATING MUTATIONS IN E6-AP UBIQUITIN-PROTEIN LIGASE GENE (UBE3A) IN ANGELMAN SYNDROME

      Nature genetics
    76. HORSTHEMKE B; DITTRICH B; BUITING K
      IMPRINTING MUTATIONS ON HUMAN-CHROMOSOME-15

      Human mutation
    77. SUTCLIFFE JS; JIANG YH; GALJAARD RJ; CHRISTIAN SL; MATSUURA T; FANG P; KUBOTA T; BRESSLER J; CATTANACH B; LEDBETTER DH; BEAUDET AL
      THE E6-AP UBIQUITIN-PROTEIN LIGASE (UBE3A) GENE IS LOCALIZED WITHIN ANARROWED ANGELMAN SYNDROME CRITICAL REGION

      PCR methods and applications
    78. WATRIN F; ROECKEL N; LACROIX L; MIGNON C; MATTEI MG; DISTECHE C; MUSCATELLI F
      THE MOUSE NECDIN GENE IS EXPRESSED FROM THE PATERNAL ALLELE ONLY AND LIES IN THE 7C REGION OF THE MOUSE-CHROMOSOME-7, A REGION OF CONSERVEDSYNTENY TO THE HUMAN PRADER-WILLI-SYNDROME REGION

      European journal of human genetics
    79. WEVRICK R; FRANCKE U
      AN IMPRINTED MOUSE TRANSCRIPT HOMOLOGOUS TO THE HUMAN IMPRINTED IN PRADER-WILLI-SYNDROME (IPW) GENE

      Human molecular genetics
    80. MEGURO M; MITSUYA K; SUI H; SHIGENAMI K; KUGOH H; NAKAO M; OSHIMURA M
      EVIDENCE FOR UNIPARENTAL, PATERNAL EXPRESSION OF THE HUMAN GABA(A) RECEPTOR SUBUNIT GENES, USING MICROCELL-MEDIATED CHROMOSOME TRANSFER

      Human molecular genetics
    81. MACDONALD HR; WEVRICK R
      THE NECDIN GENE IS DELETED IN PRADER-WILLI-SYNDROME AND IS IMPRINTED IN HUMAN AND MOUSE

      Human molecular genetics
    82. KEVERNE EB
      GENOMIC IMPRINTING IN THE BRAIN

      Current opinion in neurobiology
    83. CATTANACH BM; BARR JA; BEECHEY CV; MARTIN J; NOEBELS J; JONES J
      A CANDIDATE MODEL FOR ANGELMAN-SYNDROME IN THE MOUSE

      Mammalian genome
    84. ZUBAIR M; HILTON K; SAAM JR; SURANI MA; TILGHMAN SM; SASAKI H
      STRUCTURE AND EXPRESSION OF THE MOUSE L23MRP GENE DOWNSTREAM OF THE IMPRINTED H19 GENE - BIALLELIC EXPRESSION AND LACK OF INTERACTION WITH THE H19 ENHANCERS

      Genomics
    85. BRONDUMNIELSEN K
      THE GENETIC-BASIS FOR PRADER-WILLI-SYNDROME - THE IMPORTANCE OF IMPRINTED GENES

      Acta paediatrica
    86. BARLOW DP
      COMPETITION - A COMMON MOTIF FOR THE IMPRINTING MECHANISM

      EMBO journal
    87. KOSAKI K; MCGINNISS MJ; VERAKSA AN; MCGINNIS WJ; JONES KL
      PRADER-WILLI AND ANGELMAN-SYNDROMES - DIAGNOSIS WITH A BISULFITE-TREATED METHYLATION-SPECIFIC PCR METHOD

      American journal of medical genetics
    88. BUCHHOLZ T; JACKSON J; SMITH A
      METHYLATION ANALYSIS AT 3 DIFFERENT LOCI WITHIN THE IMPRINTED REGION OF CHROMOSOME 15Q11-13

      American journal of medical genetics
    89. BARTOLOMEI MS; TILGHMAN SM
      GENOMIC IMPRINTING IN MAMMALS

      Annual review of genetics
    90. BARABASH A; ROBLEDO M; SANZ R; RENEDO M; RAMOS C; AYUSO C; BENITEZ J
      A CLINICAL, CYTOGENETIC AND MOLECULAR STU DY OF 10 PATIENTS WITH THE PRADER-WILLI-SYNDROME

      Medicina Clinica
    91. TRENT RJ; SHEFFIELD LJ; DENG ZM; KIM WS; NASSIF NT; RYCE C; WOODS CG; MICHAELIS RC; TARLETON J; SMITH A
      THE ELUSIVE ANGELMAN-SYNDROME CRITICAL REGION

      Journal of Medical Genetics
    92. GILBERT HL; BUXTON JL; CHAN CTJ; MCKAY T; COTTRELL S; RAMSDEN S; WINTER RM; PEMBREY ME; MALCOLM S
      COUNSELING DILEMMAS ASSOCIATED WITH THE MOLECULAR CHARACTERIZATION OF2 ANGELMAN-SYNDROME FAMILIES

      Journal of Medical Genetics
    93. CASSIDY SB
      PRADER-WILLI-SYNDROME

      Journal of Medical Genetics
    94. HORSTHEMKE B
      STRUCTURE AND FUNCTION OF THE HUMAN-CHROMOSOME-15 IMPRINTING CENTER

      Journal of cellular physiology
    95. DROUIN R; BOUTOUIL M; FETNI R; HOLMQUIST GP; SCOTT P; RICHER CL; LEMIEUX N
      DNA-REPLICATION ASYNCHRONY BETWEEN THE PATERNAL AND MATERNAL ALLELES OF IMPRINTED GENES DOES NOT STRADDLE THE R G TRANSITION/

      Chromosoma
    96. CONROY JM; GREBE TA; BECKER LA; TSUCHIYA K; NICHOLLS RD; BUITING K; HORSTHEMKE B; CASSIDY SB; SCHWARTZ S
      BALANCED TRANSLOCATION 46,XY,T(2-15)(Q37.2-Q11.2) ASSOCIATED WITH ATYPICAL PRADER-WILLI-SYNDROME

      American journal of human genetics
    97. GUNAYAYGUN M; CASSIDY SB; NICHOLLS RD
      PRADER-WILLI AND OTHER SYNDROMES ASSOCIATED WITH OBESITY AND MENTAL-RETARDATION

      Behavior genetics
    98. TYCKO B
      DNA METHYLATION IN GENOMIC IMPRINTING

      Mutation research-reviews in mutation research
    99. SCHUFFENHAUER S; BUCHHOLZ T; STENGELRUTKOWSKI S; BUITING K; SCHMIDT H; MEITINGER T
      A FAMILIAL DELETION IN THE PRADER-WILLI-SYNDROME REGION INCLUDING THEIMPRINTING CONTROL REGION

      Human mutation
    100. NIIKAWA N
      GENOMIC IMPRINTING AND ITS RELEVANCE TO GENETIC-DISEASES

      Japanese journal of human genetics


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Documento generato il 20/10/20 alle ore 00:55:07