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La ricerca find articoli where soggetti phrase all words 'SPORADIC' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 957 riferimenti
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    1. Bedey, DF; Watkins, BJ
      Simultaneous observations of thin ion layers and the ionospheric electric field over Sondrestrom

      JOURNAL OF GEOPHYSICAL RESEARCH-SPACE PHYSICS
    2. Hass, S; Weidemann, A; Utermann, G; Baier, G
      Intracellular apolipoprotein E affects amyloid precursor protein processing and amyloid A beta production in COS-1 cells

      MOLECULAR GENETICS AND GENOMICS
    3. Pothula, VB; Lesser, T; Mallucci, C; May, P; Foy, P
      Vestibular schwannomas in children

      OTOLOGY & NEUROTOLOGY
    4. Goedert, M
      Alpha-synuclein and neurodegenerative diseases

      NATURE REVIEWS NEUROSCIENCE
    5. Tighe, A; Johnson, VL; Albertella, M; Taylor, SS
      Aneuploid colon cancer cells have a robust spindle checkpoint

      EMBO REPORTS
    6. Gellera, C
      Genetics of ALS in Italian families

      AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS
    7. Harada, H; Nagai, NH; Tsuneizumi, M; Mikami, I; Sugano, S; Emi, M
      Identification of DMC1, a novel gene in the TOC region on 17q25.1 that shows loss of expression in multiple human cancers

      JOURNAL OF HUMAN GENETICS
    8. Yamanouchi, Y; Takano, T; Hamaguchi, H; Tokunaga, K
      A novel apolipoprotein E5 variant with a 24-bp insertion causing hyperlipidemia

      JOURNAL OF HUMAN GENETICS
    9. Hirai, H; Nakajima, S; Miyauchi, A; Nishimura, K; Shimizu, N; Shima, M; Michigami, T; Ozono, K; Okada, S
      A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia

      JOURNAL OF HUMAN GENETICS
    10. Yamagata, K; Urakami, K; Ikeda, K; Ji, Y; Adachi, Y; Arai, H; Sasaki, H; Sato, K; Nakashima, K
      High expression of apolipoprotein e mRNA in the brains with sporadic Alzheimer's disease

      DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
    11. Fujie, H; Moriya, K; Shintani, Y; Tsutsumi, T; Takayama, T; Makuuchi, M; Kimura, S; Koike, K
      Frequent beta-catenin aberration in human hepatocellular carcinoma

      HEPATOLOGY RESEARCH
    12. Ban, S; Shinohara, T; Hirai, Y; Moritaku, Y; Cologne, JB; MacPhee, DG
      Chromosomal instability in BRCA1-or BRCA2-defective human cancer cells detected by spontaneous micronucleus assay

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    13. O'Connor, DP; Kay, EW; Leader, M; Murphy, GM; Atkins, GJ; Mabruk, MJEMF
      A high degree of chromosomal instability at 13q14 in cutaneous squamous cell carcinomas: indication for a role of a tumour suppressor gene other thanRb

      JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY
    14. Zhou, QH; Mathews, JD
      Comments on "Modelling the peak of the ionospheric E-layer" by J.E. Titheridge

      JOURNAL OF ATMOSPHERIC AND SOLAR-TERRESTRIAL PHYSICS
    15. Maksyutin, SV; Fahrutdinova, AN; Sherstyukov, ON
      Es layer and dynamics of neutral atmosphere during the periods of geomagnetic disturbances

      JOURNAL OF ATMOSPHERIC AND SOLAR-TERRESTRIAL PHYSICS
    16. Wang, CY; Chu, YH
      Interferometry investigations of blob-like sporadic E plasma irregularity using the Chung-Li VHF radar

      JOURNAL OF ATMOSPHERIC AND SOLAR-TERRESTRIAL PHYSICS
    17. Hocke, K; Igarashi, K; Nakamura, M; Wilkinson, P; Wu, J; Pavelyev, A; Wickert, J
      Global sounding of sporadic E layers by the GPS/MET radio occultation experiment

      JOURNAL OF ATMOSPHERIC AND SOLAR-TERRESTRIAL PHYSICS
    18. Machuga, DW; Mathews, JD
      Numerical simulations of three-dimensional E-region ion trajectories in realistic tidal wind and E-field structures: layer formation and transport

      JOURNAL OF ATMOSPHERIC AND SOLAR-TERRESTRIAL PHYSICS
    19. Mathews, JD; Machuga, DW; Zhou, Q
      Evidence for electrodynamic linkages between spread-F, ion rain, the intermediate layer, and sporadic E: results from observations and simulations

      JOURNAL OF ATMOSPHERIC AND SOLAR-TERRESTRIAL PHYSICS
    20. Kunugi, H; Ueki, A; Otsuka, M; Isse, K; Hirasawa, H; Kato, N; Nabika, T; Kobayashi, S; Nanko, S
      A novel polymorphism of the brain-derived neurotrophic factor (BDNF) gene associated with late-onset Alzheimer's disease

      MOLECULAR PSYCHIATRY
    21. Nakayama, T; Minato, M; Nakagawa, M; Soma, M; Tobe, H; Aoi, N; Kosuge, K; Sato, M; Ozawa, Y; Kanmatsuse, K; Kokubun, S
      A novel mutation in Ca2+-sensing receptor gene in familial hypocalciuric hypercalcemia

      ENDOCRINE
    22. Gilman, S
      Biochemical changes in multiple system atrophy detected with positron emission tomography

      PARKINSONISM & RELATED DISORDERS
    23. Lumachi, F; Ermani, M; Basso, S; Zucchetta, P; Borsato, N; Favia, G
      Localization of parathyroid tumours in the minimally invasive era: which technique should be chosen? Population-based analysis of 253 patients undergoing parathyroidectomy and factors affecting parathyroid gland detection

      ENDOCRINE-RELATED CANCER
    24. Dickson, DW
      alpha-Synuclein and the Lewy body disorders

      CURRENT OPINION IN NEUROLOGY
    25. Schuchat, A; Hilger, T; Zell, E; Farley, MM; Reingold, A; Harrison, L; Lefkowitz, L; Danila, R; Stefonek, K; Barrett, N; Morse, D; Pinner, R
      Active bacterial core surveillance of the emerging infections program network

      EMERGING INFECTIOUS DISEASES
    26. Virmani, AK; Rathi, A; Sathyanarayana, UG; Padar, A; Huang, CX; Cunnigham, HT; Farinas, AJ; Milchgrub, S; Euhus, DM; Gilcrease, M; Herman, J; Minna, JD; Gazdar, AF
      Aberrant methylation of the adenomatous polyposis coli (APC) gene promoter1A in breast and lung carcinomas

      CLINICAL CANCER RESEARCH
    27. Takayasu, H; Horie, H; Hiyama, E; Matsunaga, T; Hayashi, Y; Watanabe, Y; Suita, S; Kaneko, M; Sasaki, F; Hashizume, K; Ozaki, T; Furuuchi, K; Tada, M; Ohnuma, N; Nakagawara, A
      Frequent deletions and mutations of the beta-catenin gene are associated with overexpression of cyclin D1 and fibronectin and poorly differentiated histology in childhood hepatoblastoma

      CLINICAL CANCER RESEARCH
    28. Rengucci, C; Maiolo, P; Saragoni, L; Zoli, W; Amadori, D; Calistri, D
      Multiple detection of genetic alterations in turners and stool

      CLINICAL CANCER RESEARCH
    29. Monz, D; Munnia, A; Comtesse, N; Fischer, U; Steudel, WI; Feiden, W; Glass, B; Meese, EU
      Novel tankyrase-related gene detected with meningioma-specific sera

      CLINICAL CANCER RESEARCH
    30. Yoo, D; Willson, P; Pei, YL; Hayes, MA; Deckert, A; Dewey, CE; Friendship, RM; Yoon, YH; Gottschalk, M; Yason, C; Giulivi, A
      Prevalence of hepatitis E virus antibodies in Canadian swine herds and identification of a novel variant of swine hepatitis E virus

      CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY
    31. Goudeau, B; Dagvadorj, A; Rodrigues-Lima, F; Nedellec, P; Casteras-Simon, M; Perret, E; Langlois, S; Goldfarb, L; Vicart, P
      Structural and functional analysis of a new desmin variant causing desmin-related myopathy

      HUMAN MUTATION
    32. Yang, HF; Kaelin, WG
      Molecular pathogenesis of the von Hippel-Lindau hereditary cancer syndrome: Implications for oxygen sensing

      CELL GROWTH & DIFFERENTIATION
    33. Borg, A
      Molecular and pathological characterization of inherited breast cancer

      SEMINARS IN CANCER BIOLOGY
    34. Ishibe, N; Sgambati, MT; Fontaine, L; Goldin, LR; Jain, N; Weissman, N; Marti, GE; Caporso, NE
      Clinical characteristics of familial B-CLL in the National Cancer Institute Familial Registry

      LEUKEMIA & LYMPHOMA
    35. Chang, T
      An example of resonances, coherent structures and topological phase transitions - the origin of the low frequency broadband spectrum in the auroral zone

      NONLINEAR PROCESSES IN GEOPHYSICS
    36. Idikio, HA
      Expression of DNA mismatch repair proteins hMSH2 and hMLH1 and the cyclin G1 inhibitor, p21(waf1/cip1) in pediatric tumors: Correlation with responseto therapy

      ONCOLOGY REPORTS
    37. Abe, Y; Masuda, H; Okubo, R
      Microsatellite instability of each tumor in sporadic synchronous multiple colorectal cancers

      ONCOLOGY REPORTS
    38. Van der Looij, M; Papp, J; Sztan, M; Pulay, T; Elfadil, I; Besznyak, I; Toth, J; Devilee, P; Olah, E
      Allelic imbalance and microsatellite instability in BRCA1 associated breast and ovarian tumors

      INTERNATIONAL JOURNAL OF ONCOLOGY
    39. Prince, JA; Feuk, L; Sawyer, SL; Gottfries, J; Ricksten, A; Nagga, K; Bogdanovic, N; Blennow, K; Brookes, AJ
      Lack of replication of association findings in complex disease: an analysis of 15 polymorphisms in prior candidate genes for sporadic Alzheimer's disease

      EUROPEAN JOURNAL OF HUMAN GENETICS
    40. Starr, JM; Rush, M; De Mey, R; Dennis, MS
      Parental causes of death in stroke

      CEREBROVASCULAR DISEASES
    41. Clayton, RN; Farrell, WE
      Clonality of pituitary tumours: More complicated than initially envisaged?

      BRAIN PATHOLOGY
    42. de Gruijl, FR; van Kranen, HJ; Mullenders, LHF
      UV-induced DNA damage, repair, mutations and oncogenic pathways in skin cancer

      JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY
    43. Gutmann, DH; Hirbe, AC; Huang, ZY; Haipek, CA
      The protein 4.1 tumor suppressor, DAL-1, impairs cell motility, but regulates proliferation in a cell-type-specific fashion

      NEUROBIOLOGY OF DISEASE
    44. Gutmann, DH; Haipek, CA; Burke, SP; Sun, CX; Scoles, DR; Pulst, SM
      The NF2 interactor, hepatocyte growth factor-regulated tyrosine kinase substrate (HRS), associates with merlin in the 'open' conformation and suppresses cell growth and motility

      HUMAN MOLECULAR GENETICS
    45. Gutmann, DH
      The neurofibromatoses: when less is more

      HUMAN MOLECULAR GENETICS
    46. Friedrich, CA
      Genotype-phenotype correlation in von Hippel-Lindau syndrome

      HUMAN MOLECULAR GENETICS
    47. Gutmann, DH; Hirbe, AC; Haipek, CA
      Functional analysis of neurofibromatosis 2 (NF2) missense mutations

      HUMAN MOLECULAR GENETICS
    48. Gellera, C; Castellotti, B; Riggio, MC; Silani, V; Morandi, L; Testa, D; Casali, C; Taroni, F; Di Donato, S; Zeviani, M; Mariotti, C
      Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutations

      NEUROMUSCULAR DISORDERS
    49. Rastad, J; Ekbom, A; Hultin, H; Wuu, J; Lundgren, E; Hsieh, CC; Lambe, M
      Childbearing and the risk of parathyroid adenoma - a dominant cause for primary hyperparathyroidism

      JOURNAL OF INTERNAL MEDICINE
    50. Gentile, M; Ahnstrom, M; Schon, F; Wingren, S
      Candidate tumour suppressor genes at 11q23-q24 in breast cancer: evidence of alterations in PIG8, a gene involved in p53-induced apoptosis

      ONCOGENE
    51. Atlas, E; Stramwasser, M; Mueller, CR
      A CREB site in the BRCA1 proximal promoter acts as a constitutive transcriptional element

      ONCOGENE
    52. Suen, TC; Goss, PE
      Identification of a novel transcriptional repressor element located in thefirst intron of the human BRCA1 gene

      ONCOGENE
    53. DiNardo, DNM; Butcher, DT; Robinson, DP; Archer, TK; Rodenhiser, DI
      Functional analysis of CpG methylation in the BRCA1 promoter region

      ONCOGENE
    54. Signori, E; Bagni, C; Papa, S; Primerano, B; Rinaldi, M; Amaldi, F; Fazio, VM
      A somatic mutation in the 5 ' UTR of BRCA1 gene in sporadic breast cancer causes down-modulation of translation efficiency

      ONCOGENE
    55. Cheng, CW; Wu, PE; Yu, JC; Huang, CS; Yue, CT; Wu, CW; Shen, CY
      Mechanisms of inactivation of E-cadherin in breast carcinoma: modificationof the two-hit hypothesis of tumor suppressor gene

      ONCOGENE
    56. Derwahl, M; Studer, H
      Nodular goiter and goiter nodules: Where iodine deficiency falls short of explaining the facts

      EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES
    57. Kalinin, VN; Amosenko, FA; Shabanov, MA; Lubchenko, LN; Hosch, SB; Garkavtseva, RF; Izbicki, JR
      Three novel mutations in the RET proto-oncogene

      JOURNAL OF MOLECULAR MEDICINE-JMM
    58. Sakai, T; Wakizaka, A; Nirasawa, Y
      Congenital central hypoventilation syndrome associated with Hirschsprung'sdisease: Mutation analysis of the RET and endothelin-signaling pathways

      EUROPEAN JOURNAL OF PEDIATRIC SURGERY
    59. Weller, M
      Construction of large permutation representations for matrix groups II

      APPLICABLE ALGEBRA IN ENGINEERING COMMUNICATION AND COMPUTING
    60. Zagury, A; Neto, JGB
      Idiopathic carpotarsal osteolysis with nephropathy

      PEDIATRIC NEPHROLOGY
    61. Houillier, P; Eladari, D; Maruani, G
      Physiology and pathophysiology of the calcium-sensing receptor.

      ARCHIVES DE PEDIATRIE
    62. Tabares-Seisdedos, R; Balanza-Martinez, V; Pallardo, Y; Salazar-Fraile, J; Selva, G; Vilela, C; Vallet, M; Leal, C; Gomez-Beneyto, M
      Similar effect of family history of psychosis on Sylvian fissure size and auditory P200 amplitude in schizophrenic and bipolar subjects

      PSYCHIATRY RESEARCH-NEUROIMAGING
    63. Sommer, SS; Scaringe, WA; Hill, KA
      Human germline mutation in the factor IX gene

      MUTATION RESEARCH-DNA REPAIR
    64. Mikami, I; Harada, H; Nagai, H; Tsuneizumi, M; Nobe, Y; Koizumi, K; Sugano, S; Tanaka, S; Emi, M
      Down-regulation in multiple human cancers of a novel gene, DMHC, from 17q25.1 that encodes an integral membrane protein

      JAPANESE JOURNAL OF CANCER RESEARCH
    65. Russo, J; Hu, YF; Tahin, Q; Mihaila, D; Slater, C; Lareef, MH; Russo, IH
      Carcinogenicity of estrogens in human breast epithelial cells

      APMIS
    66. Russo, J; Hu, YF; Tahin, Q; Mihaila, D; Slater, C; Lareef, MH; Russo, IH
      Carcinogenicity of estrogens in human breast epithelial cells

      APMIS
    67. Krahn, G; Leiter, U; Udart, M; Kaskel, P; Peter, RU
      UVB-induced decrease of p16/CDKN2A expression in skin cancer patients

      PIGMENT CELL RESEARCH
    68. Peiro, G; Diebold, J; Mayr, D; Baretton, GB; Kimmig, R; Schmidt, M; Lohrs, U
      Prognostic relevance of hMLH1, hMSH2, and BAX protein expression in endometrial carcinoma

      MODERN PATHOLOGY
    69. Ascano, JJ; Frierson, H; Moskaluk, CA; Harper, JC; Roviello, F; Jackson, CE; El-Rifai, W; Vindigni, C; Tosi, P; Powell, SM
      Inactivation of the E-cadherin gene in sporadic diffuse-type gastric cancer

      MODERN PATHOLOGY
    70. Guo, SS; Sawicki, MP
      Molecular and genetic mechanism of tumorigenesis in Multiple Endocrine Neoplasia type-1

      MOLECULAR ENDOCRINOLOGY
    71. Chu, CW; Hwang, SJ; Luo, JC; Wang, YJ; Lu, RH; Lai, CR; Tsay, SH; Wu, JC; Chang, FY; Lee, SD
      Comparison of clinical, virologic and pathologic features in patients withacute hepatitis B and C

      JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY
    72. Castera, L; Pawlotsky, JM
      Hepatitis E virus infection: epidemiology and prevention

      GASTROENTEROLOGIE CLINIQUE ET BIOLOGIQUE
    73. DeGroot, LJ
      Treatment of multinodular goiter by surgery

      JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
    74. Pilipenko, V; Shalimov, S; Uyeda, S; Tanaka, H
      Possible mechanism of the over-horizon reception of FM radio waves during earthquake preparation period

      PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES
    75. Smith, JL
      A review of hepatitis E virus

      JOURNAL OF FOOD PROTECTION
    76. Ferro, P; dell'Eva, R; Pfeffer, U
      Are there CAG repeat expansion-related disorders outside the central nervous system?

      BRAIN RESEARCH BULLETIN
    77. Frenzel, S; Apel, TW; Heidemann, PH; Zerres, K; Neumann, HPH; Dorr, HG
      Phaeochromocytoma associated with a de novo VHL mutation as form fruste ofvon Hippel-Lindau disease

      EUROPEAN JOURNAL OF PEDIATRICS
    78. Wong, NACS; Harrison, DJ
      Colorectal neoplasia in ulcerative colitis - recent advances

      HISTOPATHOLOGY
    79. Yaar, M; Gilchrest, BA
      Ageing and photoageing of keratinocytes and melanocytes

      CLINICAL AND EXPERIMENTAL DERMATOLOGY
    80. Chandrasekharappa, SC; Teh, BT
      Clinical and molecular aspects of multiple endocrine neoplasia type 1

      GENETIC DISORDERS OF ENDOCRINE NEOPLASIA
    81. Iliopoulos, O
      Von Hippel-Lindau disease: Genetic and clinical observations

      GENETIC DISORDERS OF ENDOCRINE NEOPLASIA
    82. Zang, KD
      Meningioma: a cytogenetic model of a complex benign human tumor, includingdata on 394 karyotyped cases

      CYTOGENETICS AND CELL GENETICS
    83. Kolsch, H; Ludwig, M; Lutjohann, D; Rao, ML
      Neurotoxicity of 24-hydroxycholesterol, an important cholesterol elimination product of the brain, may be prevented by vitamin E and estradiol-17 beta

      JOURNAL OF NEURAL TRANSMISSION
    84. Hes, FJ; Lips, CJM; van der Luijt, RB
      Molecular genetic aspects of Von Hippel-Lindau (VHL) disease and criteria for DNA analysis in subjects at risk

      NETHERLANDS JOURNAL OF MEDICINE
    85. Chew, SL
      Paraganglioma genes

      CLINICAL ENDOCRINOLOGY
    86. Chang, T
      Colloid-like behavior and topological phase transitions in space plasmas: Intermittent low frequency turbulence in the auroral zone

      PHYSICA SCRIPTA
    87. Gras, E; Pons, C; Machin, P; Matias-Guiu, X; Prat, J
      Loss of heterozygosity at the RB-1 locus and pRB immunostaining in epithelial ovarian tumors: A molecular, immunohistochemical, and clinicopathologicstudy

      INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY
    88. Lynch, JW; Han, NLR; Haddrill, J; Pierce, KD; Schofield, PR
      The surface accessibility of the glycine receptor M2-M3 loop is increased in the channel open state

      JOURNAL OF NEUROSCIENCE
    89. Amaro, R; Schiff, ER
      Viral hepatitis

      CURRENT OPINION IN GASTROENTEROLOGY
    90. Hussein, MR; Roggero, E; Sudilovsky, EC; Tuthill, RJ; Wood, GS; Sudilovsky, O
      Alterations of mismatch repair protein expression in benign melanocytic nevi, melanocytic dysplastic nevi, and cutaneous malignant melanomas

      AMERICAN JOURNAL OF DERMATOPATHOLOGY
    91. Gimm, O; Sutter, T; Dralle, H
      Diagnosis and therapy of sporadic and familial medullary thyroid carcinoma

      JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY
    92. Wirdefeldt, K; Bogdanovic, N; Westerberg, L; Payami, H; Schalling, M; Murdoch, G
      Expression of alpha-synuclein in the human brain: relation to Lewy body disease

      MOLECULAR BRAIN RESEARCH
    93. Graves, LM; Swaminathan, B
      PulseNet standardized protocol for subtyping Listeria monocytogenes by macrorestriction and pulsed-field gel electrophoresis

      INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY
    94. Portwine, C; Chilton-MacNeill, S; Brown, C; Sexsmith, E; McLaughlin, J; Malkin, D
      Absence of germline and somatic p53 alterations in children with sporadic brain tumors

      JOURNAL OF NEURO-ONCOLOGY
    95. Sprenger, SHE; Gijtenbeek, JMM; Wesseling, P; Sciot, R; Van Calenbergh, F; Lammens, M; Jeuken, JWM
      Characteristic chromosomal aberrations in sporadic cerebellar hemangioblastomas revealed by comparative genomic hybridization

      JOURNAL OF NEURO-ONCOLOGY
    96. Lomas, J; Bello, MJ; Arjona, D; Gonzalez-Gomez, P; Alonso, ME; de Campos, JM; Vaquero, J; Ruiz-Barnes, P; Sarasa, JL; Casartelli, C; Rey, JA
      Analysis of p73 gene in meningiomas with deletion at 1p

      CANCER GENETICS AND CYTOGENETICS
    97. Suzuki, M; Ohwada, M; Saga, Y; Saito, S; Sato, I
      Are DNA mismatch repair deficiencies responsible for accumulation of genetic alterations in epithelial ovarian cancers?

      CANCER GENETICS AND CYTOGENETICS
    98. Kim, T; Chang, N; Shin, H
      Joint scheduling of garbage collector and hard real-time tasks for embedded applications

      JOURNAL OF SYSTEMS AND SOFTWARE
    99. Cohen, MM
      Asymmetry: Molecular, biologic, embryopathic, and clinical perspectives

      AMERICAN JOURNAL OF MEDICAL GENETICS
    100. Infante, J; Garcia, A; Combarros, O; Mateo, JI; Berciano, J; Sedano, MJ; Gutierrez-Rivas, EJ; Palau, F
      Diagnostic strategy for familial and sporadic cases of neuropathy associated with 17p11.2 deletion

      MUSCLE & NERVE


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Documento generato il 02/06/20 alle ore 22:56:21