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La ricerca find articoli where soggetti phrase all words 'genomic imprinting' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 268 riferimenti
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    1. Zuccotti, M; Boiani, M; Ponce, R; Guizzardi, S; Scandroglio, R; Garagna, S; Redi, CA
      Mouse Xist expression begins at zygotic genome activation and is timed by a zygotic clock

      MOLECULAR REPRODUCTION AND DEVELOPMENT
    2. Villar, AJ; Carlson, EJ; Gillespie, AM; Ursell, PC; Epstein, CJ
      Cardiomyopathy in mice with paternal uniparental disomy for chromosome 12

      GENESIS
    3. Inoue, J; Mitsuya, K; Maegawa, S; Kugoh, H; Kadota, M; Okamura, D; Shinohara, T; Nishihara, S; Takehara, S; Yamauchi, K; Schulz, TC; Oshimura, M
      Construction of 700 human/mouse A9 monochromosomal hybrids and analysis ofimprinted genes on human chromosome 6

      JOURNAL OF HUMAN GENETICS
    4. Yoshioka, H; Shirayoshi, Y; Oshimura, M
      A novel in vitro system for analyzing parental allele-specific histone acetylation in genomic imprinting

      JOURNAL OF HUMAN GENETICS
    5. Salpekar, A; Huntriss, J; Bolton, V; Monk, M
      The use of amplified cDNA to investigate the expression of seven imprintedgenes in human oocytes and preimplantation embryos

      MOLECULAR HUMAN REPRODUCTION
    6. Penkov, LI; Platonov, ES; New, DAT
      Effects of fibroblast growth factor 2 and insulin-like growth factor II onthe development of parthenogenetic mouse embryos in vitro

      IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL
    7. Killian, JK; Oka, Y; Jang, HS; Fu, XL; Waterland, RA; Sohda, T; Sakaguchi, S; Jirtle, RL
      Mannose 6-phosphate/insulin-like growth factor 2 receptor (M6P/IGF2R) variants in American and Japanese populations

      HUMAN MUTATION
    8. Rainho, CA; Kowalski, LP; Rogatto, SR
      Loss of imprinting and loss of heterozygosity on 11p15.5 in head and neck squamous cell carcinomas

      HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK
    9. Hitchins, MP; Monk, D; Bell, GM; Ali, Z; Preece, MA; Stanier, P; Moore, GE
      Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB70 in Silver-Russell syndrome

      EUROPEAN JOURNAL OF HUMAN GENETICS
    10. Wilkins, JF; Haig, D
      Genomic imprinting of two antagonistic loci

      PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    11. Sado, T; Wang, ZJ; Sasaki, H; Li, E
      Regulation of imprinted X-chromosome inactivation in mice by Tsix

      DEVELOPMENT
    12. Wutz, A; Theussl, HC; Dausman, J; Jaenisch, R; Barlow, DP; Wagner, EF
      Non-imprinted Igf2r expression decreases growth and rescues the Tme mutation in mice

      DEVELOPMENT
    13. Nolan, CM; Killian, JK; Petitte, JN; Jirtle, RL
      Imprint status of M6P/IGF2R and IGF2 in chickens

      DEVELOPMENT GENES AND EVOLUTION
    14. Westbury, J; Watkins, M; Ferguson-Smith, AC; Smith, J
      Dynamic temporal and spatial regulation of the cdk inhibitor p57(kip2) during embryo morphogenesis

      MECHANISMS OF DEVELOPMENT
    15. Kohda, A; Taguchi, H; Okumura, K
      Visualization of biallelic expression of the imprinted SNRPN gene induced by inhibitors of DNA methylation and histone deacetylation

      BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY
    16. Kohda, M; Hoshiya, H; Katoh, M; Tanaka, I; Masuda, R; Takemura, T; Fujiwara, M; Oshimura, M
      Frequent loss of imprinting of IGF2 and MEST in lung adenocarcinoma

      MOLECULAR CARCINOGENESIS
    17. Maegawa, S; Yoshioka, H; Itaba, N; Kubota, N; Nishihara, S; Shirayoshi, Y; Nanba, E; Oshimura, M
      Epigenetic silencing of PEG3 gene expression in human glioma cell lines

      MOLECULAR CARCINOGENESIS
    18. Zwart, R; Sleutels, F; Wutz, A; Schinkel, AH; Barlow, DP
      Bidirectional action of the Igf2r imprint control element on upstream and downstream imprinted genes

      GENES & DEVELOPMENT
    19. Evans, HK; Wylie, AA; Murphy, SK; Jirtle, RL
      The neuronatin gene resides in a "micro-imprinted" domain on human chromosome 20q11.2

      GENOMICS
    20. Srivastava, A; Cotton, C; Paterson, AD
      Sex- and age-of-onset-based locus heterogeneity in asthma

      GENETIC EPIDEMIOLOGY
    21. Thompson, SL; Konfortova, G; Gregory, RI; Reik, W; Dean, W; Feil, R
      Environmental effects on genomic imprinting in mammals

      TOXICOLOGY LETTERS
    22. Kobayashi, S; Uemura, H; Kohda, T; Nagai, T; Chinen, Y; Naritomi, K; Kinoshita, E; Ohashi, H; Imaizumi, K; Tsukahara, M; Sugio, Y; Tonoki, H; Kishino, T; Tanaka, T; Yamada, M; Tsutsumi, O; Niikawa, N; Kaneko-Ishino, T; Ishino, F
      No evidence of PEG1/MEST gene mutations in Silver-Russell syndrome patients

      AMERICAN JOURNAL OF MEDICAL GENETICS
    23. Kamnasaran, D
      Epigenetic inheritance associated with human chromosome 14

      CLINICAL AND INVESTIGATIVE MEDICINE-MEDECINE CLINIQUE ET EXPERIMENTALE
    24. Castrillon, DH; Sun, DQ; Weremowicz, S; Fisher, RA; Crum, CP; Genest, DR
      Discrimination of complete hydatidiform mole from its mimics by immunohistochemistry of the paternally imprinted gene product p57(KIP2)

      AMERICAN JOURNAL OF SURGICAL PATHOLOGY
    25. Hogarty, MD; Maris, JM; White, PS; Guo, C; Brodeur, GM
      Analysis of genomic imprinting at 1p35-36 in neuroblastoma

      MEDICAL AND PEDIATRIC ONCOLOGY
    26. Tanaka, K; Shiota, G; Meguro, M; Mitsuya, K; Oshimura, M; Kawasaki, H
      Loss of imprinting of long QT intronic transcript 1 in colorectal cancer

      ONCOLOGY
    27. Kotzot, D
      Complex and segmental uniparental disomy (UPD): review and lessons from rare chromosomal complements

      JOURNAL OF MEDICAL GENETICS
    28. de Koning, DJ; Harlizius, B; Rattink, AP; Groenen, MAM; Brascamp, EW; van Arendonk, JAM
      Detection and characterization of quantitative trait loci for meat qualitytraits in pigs

      JOURNAL OF ANIMAL SCIENCE
    29. John, RM; Aparicio, SAJR; Ainscough, JFX; Arney, KL; Khosla, S; Hawker, K; Hilton, KJ; Barton, SC; Surani, MA
      Imprinted expression of Neuronatin from modified BAC transgenes reveals regulation by distinct and distant enhancers

      DEVELOPMENTAL BIOLOGY
    30. Kotzot, D
      Comparative analysis of isodisomic and heterodisomic segments in cases with maternal uniparental disomy 14 suggests more than one imprinted region

      CLINICAL GENETICS
    31. Hanel, ML; Wevrick, R
      The role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndrome

      CLINICAL GENETICS
    32. Sakatani, T; Wei, M; Katoh, M; Okita, C; Wada, D; Mitsuya, K; Meguro, M; Ikeguchi, M; Ito, H; Tycko, B; Oshimura, M
      Epigenetic heterogeneity at imprinted loci in normal populations

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    33. Bygren, LO; Kaati, G; Edvinsson, S
      Longevity determined by paternal ancestors' nutrition during their slow growth period

      ACTA BIOTHEORETICA
    34. Kalousek, DK; Vekemans, M
      Confined placental mosaicism and genomic imprinting

      BEST PRACTICE & RESEARCH IN CLINICAL OBSTETRICS & GYNAECOLOGY
    35. Yatsuki, H; Watanabe, H; Hattori, M; Joh, K; Soejima, H; Komoda, H; Xin, ZH; Zhu, X; Higashimoto, K; Nishimura, M; Kuratomi, S; Sasaki, H; Sakaki, Y; Mukai, T
      Sequence-based structural features between Kvlqt1 and Tapa1 on mouse chromosome 7F4/F5 corresponding to the Beckwith-Wiedemann syndrome region on human 11p15.5: Long-stretches of unusually well conserved intronic sequences of Kvlqt1 between mouse and human

      DNA RESEARCH
    36. Mayer, W; Hemberger, M; Frank, HG; Grummer, R; Winterhager, E; Kaufmann, P; Fundele, R
      Expression of the imprinted genes MEST/Mest in human and murine placenta suggests a role in angiogenesis

      DEVELOPMENTAL DYNAMICS
    37. Goto, Y; Takagi, N
      Maternally inherited X chromosome is not inactivated in mouse blastocysts due to parental imprinting

      CHROMOSOME RESEARCH
    38. Haig, D; Wilkins, JF
      Genomic imprinting, sibling solidarity and the logic of collective action

      PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    39. Vernucci, M; Cerrato, F; Besnard, N; Casola, S; Pedone, PV; Bruni, CB; Riccio, A
      The H19 endodermal enhancer is required for Igf2 activation and tumor formation in experimental liver carcinogenesis

      ONCOGENE
    40. Okamoto, I; Tan, SS; Takagi, N
      X-chromosome inactivation in XX androgenetic mouse embryos surviving implantation

      DEVELOPMENT
    41. Drewell, RA; Brenton, JD; Ainscough, JFX; Barton, SC; Hilton, KJ; Arney, KL; Dandolo, L; Surani, MA
      Deletion of a silencer element disrupts H19 imprinting independently of a DNA methylation epigenetic switch

      DEVELOPMENT
    42. Petronis, A
      The genes for major psychosis: Aberrant sequence or regulation?

      NEUROPSYCHOPHARMACOLOGY
    43. Schmidt, JV; Matteson, PG; Jones, BK; Guan, XT; Tilghman, SM
      The Dlk1 and Gtl2 genes are linked and reciprocally imprinted

      GENES & DEVELOPMENT
    44. Srivastava, R; Hsieh, S; Grinberg, A; Williams-Simons, L; Huang, SP; Pfeifer, K
      H19 and Igf2 monoallelic expression is regulated in two distinct ways by ashared cis acting regulatory region upstream of H19

      GENES & DEVELOPMENT
    45. Nakada, Y; Taniura, H; Uetsuki, T; Yoshikawa, K
      Characterization and chromosomal mapping of a human necdin pseudogene

      GENE
    46. Weinstein, LS; Yu, SH; Ecelbarger, CA
      Variable imprinting of the heterotrimeric G protein G(s) alpha-subunit within different segments of the nephron

      AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY
    47. Schiffer, HH; Swanson, GT; Masliah, E; Heinemann, SF
      Unequal expression of allelic kainate receptor GluR7 mRNAs in human brains

      JOURNAL OF NEUROSCIENCE
    48. Fisher, RA; Khatoon, R; Paradinas, FJ; Roberts, AP; Newlands, ES
      Repetitive complete hydatidiform mole can be biparental in origin and either male or female

      HUMAN REPRODUCTION
    49. Banerjee, S; Lamond, S; McMahon, A; Campbell, S; Nargund, G
      Does blastocyst culture eliminate paternal chromosomal defects and select good embryos? Inheritance of an abnormal paternal genome following ICSI

      HUMAN REPRODUCTION
    50. Sinclair, KD; Young, LE; Wilmut, I; McEvoy, TG
      In-utero overgrowth in ruminants following embryo culture: lessons from mice and a warning to men

      HUMAN REPRODUCTION
    51. Liang, L; Kanduri, C; Pilartz, M; Svensson, K; Song, JH; Wentzel, P; Eriksson, U; Ohlsson, R
      Dynamic readjustment of parental methylation patterns of the 5 '-flank of the mouse H19 gene during in vitro organogenesis

      INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY
    52. Hatada, I; Mukai, T
      Genomic imprinting and Beckwith-Wiedemann syndrome

      HISTOLOGY AND HISTOPATHOLOGY
    53. Hu, JF; Ulaner, GA; Oruganti, H; Ivaturi, RD; Balagura, KA; Pham, J; Vu, TH; Hoffman, AR
      Allelic expression of the putative tumor suppressor gene p73 in human fetal tissues and tumor specimens

      BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION
    54. Alleman, M; Doctor, J
      Genomic imprinting in plants: observations and evolutionary implications

      PLANT MOLECULAR BIOLOGY
    55. Kornberg, JR; Brown, JL; Sadovnick, AD; Remick, RA; Keck, PE; McElroy, SL; Rapaport, MH; Thompson, PM; Kaul, JB; Vrabel, CM; Schommer, SC; Wilson, T; Pizzuco, D; Jameson, S; Schibuk, L; Kelsoe, JR
      Evaluating the parent-of-origin effect in bipolar affective disorder - Is a more penetrant subtype transmitted paternally?

      JOURNAL OF AFFECTIVE DISORDERS
    56. 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
    57. Ariel, I; de Groot, N; Hochberg, A
      Imprinted H19 gene expression in embryogenesis and human cancer: The oncofetal connection

      AMERICAN JOURNAL OF MEDICAL GENETICS
    58. Moore, ES; Ward, RE; Escobar, LF; Carlin, ME
      Heterogeneity in Wiedemann-Beckwith syndrome: Anthropometric evidence

      AMERICAN JOURNAL OF MEDICAL GENETICS
    59. Gilchrist, D; Glerum, DM; Wevrick, R
      Deconstructing Mendel: new paradigms in genetic mechanisms

      CLINICAL AND INVESTIGATIVE MEDICINE-MEDECINE CLINIQUE ET EXPERIMENTALE
    60. Clapcott, SJ; Teale, AJ; Kemp, SJ
      Evidence for genomic imprinting of the major QTL controlling susceptibility to trypanosomiasis in mice

      PARASITE IMMUNOLOGY
    61. Murphy, SK; Jirtle, RL
      Imprinted genes as potential genetic and epigenetic toxicologic targets

      ENVIRONMENTAL HEALTH PERSPECTIVES
    62. Takano, Y; Shiota, G; Kawasaki, H
      Analysis of genomic imprinting of insulin-like growth factor 2 in colorectal cancer

      ONCOLOGY
    63. Weiss, U; Ischia, R; Eder, S; Lovisetti-Scamihorn, P; Bauer, R; Fischer-Colbrie, R
      Neuroendocrine secretory protein 55 (NESP55): Alternative splicing onto transcripts of the GNAS gene and posttranslational processing of a maternallyexpressed protein

      NEUROENDOCRINOLOGY
    64. Lerch, N; Bosch, N; Muller, H; Malik, NJ
      Molecular genetic diagnosis of Prader-Willi and Angelman syndrome using a methylation-specific polymerase chain reaction

      MONATSSCHRIFT KINDERHEILKUNDE
    65. Nemtsova, MV
      Genomic imprinting and human hereditary disorders

      MOLECULAR BIOLOGY
    66. Nogami, M; Kohda, A; Taguchi, H; Nakao, M; Ikemura, T; Okumura, K
      Relative locations of the centromere and imprinted SNRPN gene within chromosome 15 territories during the cell cycle in HL60 cells

      JOURNAL OF CELL SCIENCE
    67. Xin, ZG; Soejima, H; Higashimoto, K; Yatsuki, H; Zhu, XK; Satoh, Y; Masaki, Z; Kaneko, Y; Jinno, Y; Fukuzawa, R; Hata, J; Mukai, T
      A novel imprinted gene, KCNQ1DN, within the WT2 critical region of human chromosome 11p15.5 and its reduced expression in Wilms' tumors

      JOURNAL OF BIOCHEMISTRY
    68. Sasaki, H; Ishihara, K; Kato, R
      Mechanisms of Igf2/H19 imprinting: DNA methylation, chromatin and long-distance gene regulation

      JOURNAL OF BIOCHEMISTRY
    69. Okutsu, T; Kuroiwa, Y; Kagitani, F; Kai, M; Aisaka, K; Tsutsumi, O; Kaneko, Y; Yokomori, K; Surani, MA; Kohda, T; Kaneko-Ishino, T; Ishino, F
      Expression and imprinting status of human PEG8/IGF2AS, a paternally expressed antisense transcript from the IGF2 locus, in Wilms' tumors

      JOURNAL OF BIOCHEMISTRY
    70. Gregorova, S; Forejt, J
      PWD/Ph and PWK/Ph inbred mouse strains of Mus m-musculus subspecies - a valuable resource of phenotypic variations and genomic polymorphisms

      FOLIA BIOLOGICA
    71. Burton, TL; Husband, BC
      Fitness differences among diploids, tetraploids, and their triploid progeny in Chamerion angustifolium: Mechanisms of inviability and implications for polyploid evolution

      EVOLUTION
    72. Buiting, K; Farber, C; Kroisel, P; Wagner, K; Brueton, L; Robertson, ME; Lich, C; Horsthemke, B
      Imprinting centre deletions in two PWS families: implications for diagnostic testing and genetic counselling

      CLINICAL GENETICS
    73. Hattori, H; Matsuzaki, A; Suminoe, A; Ihara, K; Eguchi, M; Tajiri, T; Suita, S; Ishii, E; Hara, T
      Genomic imprinting of insulin-like growth factor-2 in infant leukemia and childhood neuroblastoma

      CANCER
    74. Malik, K; Brown, KW
      Epigenetic gene deregulation in cancer

      BRITISH JOURNAL OF CANCER
    75. Ross, JA; Radloff, GA; Davies, SM
      H19 and IGF-2 allele-specific expression in hepatoblastoma

      BRITISH JOURNAL OF CANCER
    76. 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
    77. Kondoh, M; Higashi, M
      Reproductive isolation mechanism resulting from resolution of intragenomicconflict

      AMERICAN NATURALIST
    78. Iwasa, Y; Mochizuki, A; Takeda, Y
      The evolution of genomic imprinting: Abortion and overshoot explain aberrations

      EVOLUTIONARY ECOLOGY RESEARCH
    79. Sasaki, T; Nemoto, M; Yamasaki, K; Tajima, N
      Preferential transmission of maternal allele with DQA1*0301-DQB1*0302 haplotype to affected offspring in families with type 1 diabetes

      JOURNAL OF HUMAN GENETICS
    80. Pulford, DJ; Falls, JG; Killian, JK; Jirtle, RL
      Polymorphisms, genomic imprinting and cancer susceptibility

      MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH
    81. Lossie, AC; Driscoll, DJ
      Transmission of Angelman syndrome by an affected mother

      GENETICS IN MEDICINE
    82. Haig, D
      Asymmetric relations: Internal conflicts and the horror of incest

      EVOLUTION AND HUMAN BEHAVIOR
    83. Lord, RSA; Chambers, AJ
      Familial carotid body paragangliomas and sensorineural hearing-loss: a newsyndrome

      CARDIOVASCULAR SURGERY
    84. Lemaire, M; Persu, A; Hainaut, P; De Plaen, JF
      Hereditary paraganglioma

      JOURNAL OF INTERNAL MEDICINE
    85. Sullivan, MJ; Taniguchi, T; Jhee, A; Kerr, N; Reeve, AE
      Relaxation of IGF2 imprinting in Wilms tumours associated with specific changes in IGF2 methylation

      ONCOGENE
    86. Ohlsson, R; Flam, F; Fisher, R; Miller, S; Cui, HM; Pfeifer, S; Adam, GIR
      Random monoallelic expression of the imprinted IGF2 and H19 genes in the absence of discriminative parental marks

      DEVELOPMENT GENES AND EVOLUTION
    87. 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
    88. Caspary, T; Cleary, MA; Perlman, EJ; Zhang, PM; Elledge, SJ; Tilghman, SM
      Oppositely imprinted genes p57(Kip2) and Igf2 interact in a mouse model for Beckwith-Wiedemann syndrome

      GENES & DEVELOPMENT
    89. Vielle-Calzada, JP; Thomas, J; Spillane, C; Coluccio, A; Hoeppner, MA; Grossniklaus, U
      Maintenance of genomic imprinting at the Arabidopsis medea locus requires zygotic DDM1 activity

      GENES & DEVELOPMENT
    90. Moore, GE; Abu-Amero, S; Wakeling, E; Hitchins, M; Monk, D; Stanier, P; Preece, M
      The search for the gene for Silver-Russell syndrome

      ACTA PAEDIATRICA
    91. Nicholls, RD; Ohta, T; Gray, TA
      Genetic abnormalities in Prader-Willi syndrome and lessons from mouse models

      ACTA PAEDIATRICA
    92. Mannens, M; Alders, M
      Genomic imprinting: concept and clinical consequences

      ANNALS OF MEDICINE
    93. Paterson, AD; Petronis, A
      Sex-based linkage analysis of alcoholism

      GENETIC EPIDEMIOLOGY
    94. Hershko, A; Razin, A; Shemer, R
      Imprinted methylation and its effect on expression of the mouse Zfp127 gene

      GENE
    95. Nishita, Y; Sado, T; Yoshida, I; Takagi, N
      Effect of CpG methylation on expression of the mouse imprinted gene Mest

      GENE
    96. Tanos, V; Prus, D; Ayesh, S; Weinstein, D; Tykocinski, ML; De-Groot, N; Hochberg, A; Ariel, I
      Expression of the imprinted H19 oncofetal RNA in epithelial ovarian cancer

      EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY
    97. Shamanski, FL; Kimura, Y; Lavoir, MC; Pedersen, RA; Yanagimachi, R
      Status of genomic imprinting in mouse spermatids

      HUMAN REPRODUCTION
    98. Latham, KE; Kutyna, K; Wang, QX
      Genetic variation in trophectoderm function in parthenogenetic mouse embryos

      DEVELOPMENTAL GENETICS
    99. Haghighi, F; Fyer, AJ; Weissman, MM; Knowles, JA; Hodge, SE
      Parent-of-origin effect in panic disorder

      AMERICAN JOURNAL OF MEDICAL GENETICS
    100. Kotzot, D
      Abnormal phenotypes in uniparental disomy (UPD): Fundamental aspects and acritical review with bibliography of UPD other than 15

      AMERICAN JOURNAL OF MEDICAL GENETICS


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Documento generato il 17/02/20 alle ore 08:25:59