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La ricerca find articoli where soggetti phrase all words 'FANCONI-ANEMIA' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 240 riferimenti
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    1. Moses, RE
      DNA damage processing defects and disease

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    2. Yamada, K; Olsen, JC; Patel, M; Rao, KW; Walsh, CE
      Functional correction of Fanconi anemia group C hematopoietic cells by theuse of a novel lentiviral vector

      MOLECULAR THERAPY
    3. Noll, M; Bateman, RL; D'Andrea, AD; Grompe, M
      Preclinical protocol for in vivo selection of hematopoietic stem cells corrected by gene therapy in Fanconi anemia group C

      MOLECULAR THERAPY
    4. Ren, J; Youssoufian, H
      Functional analysis of the putative peroxidase domain of FANCA, the Fanconi anemia complementation group A protein

      MOLECULAR GENETICS AND METABOLISM
    5. Storb, R; Blume, KG; O'Donnell, MR; Chauncey, T; Forman, SJ; Deeg, HJ; Hu, WW; Appelbaum, FR; Doney, K; Flowers, MED; Sanders, J; Leisenring, W
      Cyclophosphamide and antithymocyte globulin to condition patients with aplastic anemia for allogeneic marrow transplantations: The experience in fourcenters

      BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
    6. McDermott, MB; Corbally, MT; O'Marcaigh, AS
      Extracutaneous Sweet syndrome involving the gastrointestinal tract in a patient with Fanconi anemia

      JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
    7. Friedlander, PL
      Genomic instability in head and neck cancer patients

      HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK
    8. Roxo, P; Arruda, LK; Nagao, AT; Carneiro-Sampaio, MMS; Ferriani, VPL
      Allergic and immunologic parameters in patients with Fanconi's anemia

      INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY
    9. Tercanli, S; Miny, P; Siebert, MS; Hosli, I; Surbek, DV; Holzgreve, W
      Fanconi anemia associated with increased nuchal translucency detected by first-trimester ultrasound

      ULTRASOUND IN OBSTETRICS & GYNECOLOGY
    10. Kohn, DB
      Gene therapy for genetic haematological disorders and immunodeficiencies

      JOURNAL OF INTERNAL MEDICINE
    11. Tercanli, S; Troeger, C; Fahnenstich, H; Hosli, I; Holzgreve, W
      Prenatal diagnosis and management of VACTERL-Association

      ZEITSCHRIFT FUR GEBURTSHILFE UND NEONATOLOGIE
    12. Mondovits, B; Vermylen, C; Brichard, B; Cornu, G
      Bone marrow transplantation in Fanconi's anemia: about seven cases

      ARCHIVES DE PEDIATRIE
    13. Mondovits, B; Vermylen, C; Brichard, B; Cornu, G
      Molecular biology's contribution to the understanding and treatment of Fanconi anemia

      ARCHIVES DE PEDIATRIE
    14. Yamashita, T; Nakahata, T
      Current knowledge on the pathophysiology of Fanconi anemia: From genes to phenotypes

      INTERNATIONAL JOURNAL OF HEMATOLOGY
    15. Busch, DB; Ziffer, DW; Coleman, D; Wills, L; McDonough, HG; Jones, NJ
      Phenotype of FAECB (Facility for Automated Experiments in Cell Biology) Chinese hamster ovary mutants with minimal UV-sensitivity

      MUTATION RESEARCH-DNA REPAIR
    16. Dronkert, MLG; Kanaar, R
      Repair of DNA interstrand cross-links

      MUTATION RESEARCH-DNA REPAIR
    17. Kelley, MR; Tritt, R; Xu, Y; New, S; Freie, B; Clapp, DW; Deutsch, WA
      The Drosophila S3 multifunctional DNA repair/ribosomal protein protects Fanconi anemia cells against oxidative DNA damaging agents

      MUTATION RESEARCH-DNA REPAIR
    18. Pincheira, J; Bravo, M; Santos, MJ; de la Torre, C; Lopez-Saez, JF
      Fanconi anemia lymphocytes: effect of DL-alpha-tocopherol (Vitamin E) on chromatid breaks and on G(2) repair efficiency

      MUTATION RESEARCH-DNA REPAIR
    19. Kapur, RP
      Practicing pediatric pathology without a microscope

      MODERN PATHOLOGY
    20. Bale, SJ; Digiovanna, JJ
      Cancer-associated genodermatoses and familial cancer syndromes with cutaneous manifestations

      CLINICS IN DERMATOLOGY
    21. Ellis, NA; Ciocci, S; German, J
      Back mutation can produce phenotype reversion in Bloom syndrome somatic cells

      HUMAN GENETICS
    22. Smith, J; Baldeyron, C; De Oliveira, I; Sala-Trepat, M; Papadopoulo, D
      The influence of DNA double-strand break structure on end-joining in humancells

      NUCLEIC ACIDS RESEARCH
    23. Zyuzikov, NA; Prise, KM; Zdzienicka, MZ; Newman, HC; Michael, BD; Trott, KR
      The relationship between the RBE of alpha particles and the radiosensitivity of different mutations of Chinese hamster cells

      RADIATION AND ENVIRONMENTAL BIOPHYSICS
    24. Wang, X; Peterson, CA; Zheng, HY; Nairn, RS; Legerski, RJ; Li, L
      Involvement of nucleotide excision repair in a recombination-independent and error-prone pathway of DNA interstrand cross-link repair

      MOLECULAR AND CELLULAR BIOLOGY
    25. Yoshimasu, T; Tanaka, R; Suenobu, S; Yagasaki, H; Yoshino, H; Ueda, T; Hisakawa, H; Ishii, T; Mitsui, T; Ebihara, Y; Manabe, A; Iseki, T; Maekawa, T; Nakahata, T; Asano, S; Tsuji, K
      Prompt and durable hematopoietic reconstitution by unrelated cord blood transplantation in a child with Fanconi anemia

      BONE MARROW TRANSPLANTATION
    26. Vlachos, A; Federman, N; Reyes-Haley, C; Abramson, J; Lipton, JM
      Hematopoietic stem cell transplantation for diamond blackfan anemia: a report from the diamond blackfan anemia registry

      BONE MARROW TRANSPLANTATION
    27. Ayas, M; Solh, H; Mustafa, MM; Al-Mahr, M; Al-Fawaz, I; Al-Jefri, A; Shalaby, L; Al-Nasser, A; Al-Sedairy, R
      Bone marrow transplantation from matched siblings in patients with Fanconianemia utilizing low-dose cyclophosphamide, thoracoabdominal radiation andantithymocyte globulin

      BONE MARROW TRANSPLANTATION
    28. Pang, QS; Keeble, W; Christianson, TA; Faulkner, GR; Bagby, GC
      FANCC interacts with Hsp70 to protect hematopoietic cells from IFN-gamma/TNF-alpha-mediated cytotoxicity

      EMBO JOURNAL
    29. Rischewski, J; Schneppenheim, R
      Screening strategies for a highly polymorphic gene: DHPLC analysis of the Fanconi anemia group A gene

      JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS
    30. Seto, ML; Lee, SJ; Sze, RW; Cunningham, ML
      Another TWIST on Baller-Gerold syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    31. Davies, SM
      Therapy-related leukemia associated with alkylating agents

      MEDICAL AND PEDIATRIC ONCOLOGY
    32. Wajnrajch, MP; Gertner, JM; Huma, Z; Popovic, J; Lin, K; Verlander, PC; Batish, SD; Giampietro, PF; Davis, JG; New, MI; Auerbach, AD
      Evaluation of growth and hormonal status in patients referred to the International Fanconi Anemia Registry

      PEDIATRICS
    33. Nowzari, H; Jorgensen, MG; Ta, TT; Contreras, A; Slots, J
      Aggressive periodontitis associated with Fanconi's anemia. A case report

      JOURNAL OF PERIODONTOLOGY
    34. Tse, WT; Tang, J; Jin, O; Korsgren, C; John, KM; Kung, AL; Gwynn, B; Peters, LL; Lux, SE
      A new spectrin, beta IV, has a major truncated isoform that associates with promyelocytic leukemia protein nuclear bodies and the nuclear matrix

      JOURNAL OF BIOLOGICAL CHEMISTRY
    35. Adelfalk, C; Lorenz, M; Serra, V; von Zglinicki, T; Hirsch-Kauffmann, M; Schweiger, M
      Accelerated telomere shortening in Fanconi anemia fibroblasts - a longitudinal study

      FEBS LETTERS
    36. Mangiacasale, R; Tritarelli, A; Sciamanna, I; Cannone, M; Lavia, P; Barberis, MC; Lorenzini, R; Cundari, E
      Normal and cancer-prone human cells respond differently to extremely low frequency magnetic fields

      FEBS LETTERS
    37. Vit, JP; Guillouf, C; Rosselli, F
      Futile caspase-8 activation during the apoptotic cell death induced by DNAdamaging agents in human B-lymphoblasts

      EXPERIMENTAL CELL RESEARCH
    38. Pluth, JM; Fried, LM; Kirchgessner, CU
      Severe combined immunodeficient cells expressing mutant hRAD54 exhibit a marked DNA double-strand break repair and error-prone chromosome repair defect

      CANCER RESEARCH
    39. Thompson, AA; Woodruff, K; Feig, SA; Nguyen, LT; Schanen, NC
      Congenital thrombocytopenia and radio-ulnar synostosis: a new familial syndrome

      BRITISH JOURNAL OF HAEMATOLOGY
    40. Djuzenova, CS; Flentje, M
      Light scatter and DNA accessibility to propidium iodide of ataxia telangiectasia and Fanconi anemia cells

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    41. Futaki, M; Watanabe, S; Kajigaya, S; Liu, JM
      Fanconi anemia protein, FANCG, is a phosphoprotein and is upregulated withFANCA after TNF-alpha treatment

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    42. Verloes, A; Jamar, M; Dideberg, V; Herens, C
      Episphalosomic syndrome: a MCA syndrome ressembling Fanconi anemia, with increased baseline level of chromosome breaks but no hypersensivity to clastogens

      ANNALES DE GENETIQUE
    43. Edelmann, L; Wasserstein, MP; Kornreich, R; Sansaricq, C; Snyderman, SE; Diaz, GA
      Maple syrup urine disease: Identification and carrier-frequency determination of a novel founder mutation in the Ashkenazi Jewish population

      AMERICAN JOURNAL OF HUMAN GENETICS
    44. Yamada, T; Tachibana, A; Shimizu, T; Mugishima, H; Okubo, M; Sasaki, MS
      Novel mutations of the FANCG gene causing alternative splicing in JapaneseFanconi anemia

      JOURNAL OF HUMAN GENETICS
    45. Kapelushnik, J; Mandel, H; Varadi, G; Nagler, A
      Fludarabine-based protocol for haploidentical peripheral blood stem cell transplantation in Hurler syndrome

      JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
    46. Orme, L; Gorlick, R; Meyers, PA; Athanasian, E; Huvos, AG
      Osteosarcoma associated with absent thumbs: A report of two cases

      JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
    47. Pagano, G; Korkina, LG
      Prospects for nutritional interventions in the clinical management of Fanconi anemia

      CANCER CAUSES & CONTROL
    48. Martinez-Jaramillo, G; Espinoza-Hernandez, L; Benitez-Aranda, H; Mayani, H
      Long-term proliferation in vitro of hematopoietic progenitor cells from children with congenital bone marrow failure: effect of rhGM-CSF and rhEPO

      EUROPEAN JOURNAL OF HAEMATOLOGY
    49. Niedermayer, I; Reiche, W; Graf, N; Mestres, P; Feiden, W
      Cerebroretinal vasculopathy and leukoencephalopathy mimicking a brain tumor - Report of two early-onset cases with Fanconi's anemia-like phenotypes suggesting an autosomal-recessive inheritance pattern

      CLINICAL NEUROPATHOLOGY
    50. Timeus, F; Crescenzio, N; Saracco, P; Leone, L; Ponzio, G; Ramenghi, U
      Cell cycle analysis in the diagnosis of Fanconi's anemia

      HAEMATOLOGICA
    51. Guillouf, C; Vit, JP; Rosselli, F
      Loss of the Fanconi anemia group C protein activity results in an inability to activate caspase-3 after ionizing radiation

      BIOCHIMIE
    52. Rischewski, JR; Clausen, H; Leber, V; Niemeyer, C; Ritter, J; Schindler, D; Schneppenheim, R
      A heterozygous frameshift mutation in the Fanconi Anemia C gene in familiary T-ALL and secondary malignancy

      KLINISCHE PADIATRIE
    53. Irons, RD; Pyatt, DW; Stillman, WS; Som, DB; Claffey, DJ; Ruth, JA
      Comparative toxicity of known and putative metabolites of 1,3-butadiene inhuman CD34(+) bone marrow cells

      TOXICOLOGY
    54. Dronkert, MLG; de Wit, J; Boeve, M; Vasconcelos, ML; van Steeg, H; Tan, TLR; Hoeijmakers, JHJ; Kanaar, R
      Disruption of mouse SNM1 causes increased sensitivity to the DNA interstrand cross-linking agent mitomycin C

      MOLECULAR AND CELLULAR BIOLOGY
    55. Yakoub-Agha, I; Damaj, G; Garderet, L; Bonnet, J; Devergie, A; Esperou, H; Ribaud, P; Socie, G; Gluckman, E
      Severe oesophagitis after allogeneic bone marrow transplantation for Fanconi's anemia

      BONE MARROW TRANSPLANTATION
    56. Elhasid, R; Ben Arush, MW; Katz, T; Gan, Y; Shechter, Y; Sami, I; Postovsky, S; Reisner, Y; Rowe, JM
      Successful haploidentical bone marrow transplantation in Fanconi anemia

      BONE MARROW TRANSPLANTATION
    57. Speit, G; Schutz, P; Merk, O
      Induction and repair of formaldehyde-induced DNA-protein crosslinks in repair-deficient human cell lines

      MUTAGENESIS
    58. Roux, P; Novitzky, N
      The Cape Town experience with haematopoietic stem cell transplantation: The paediatric programme

      SOUTH AFRICAN MEDICAL JOURNAL
    59. Habib, Z; Abudaia, J; Bamehriz, F; Ahmed, S
      Fanconi's anemia with solitary crossed renal ectopia, vesicoureteric reflux, and genital abnormalities

      PEDIATRIC SURGERY INTERNATIONAL
    60. Akaboshi, S; Yoshimura, M; Hara, T; Kageyama, H; Nishikwa, K; Kawakami, T; Ieshima, A; Takeshita, K
      A case of Hoyeraal-Hreidarsson syndrome: Delayed myelination and hypoplasia of corpus callosum are other important signs

      NEUROPEDIATRICS
    61. Wilbur, AK
      Possible case of Rubinstein-Taybi syndrome in a prehistoric skeleton from west-central Illinois

      AMERICAN JOURNAL OF MEDICAL GENETICS
    62. Manouvrier, S; Moerman, A; Coeslier, A; Devisme, L; Boute, O; Le Merrer, M
      Radioulnar synostosis, radial ray abnormalities, and severe malformations in the male: A new X-linked dominant multiple congenital anomalies syndrome?

      AMERICAN JOURNAL OF MEDICAL GENETICS
    63. Gonzalez-del Angel, A; Cervera, M; Gomez, L; Perez-Vera, P; Orozco, L; Carnevale, A; Del Castillo, V
      Ataxia-pancytopenia syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    64. Korkina, LG; Deeva, IB; De Biase, A; Iaccarino, M; Oral, R; Warnau, M; Pagano, G
      Redox-dependent toxicity of diepoxybutane and mitomycin C in sea urchin embryogenesis

      CARCINOGENESIS
    65. Slayton, WB; Schibler, KR
      Congenital bone marrow failure syndromes associated with protean developmental defects and leukemia

      CLINICS IN PERINATOLOGY
    66. Lambert, MW; Lambert, WC
      DNA repair and chromatin structure in genetic diseases

      PROGRESS IN NUCLEIC ACID RESEARCH AND MOLECULAR BIOLOGY, VOL 63
    67. Tosal, L; Comendador, MA; Sierra, LM
      The mus308 locus of Drosophila melanogaster is implicated in the bypass ofENU-induced O-alkylpyrimidine adducts

      MOLECULAR AND GENERAL GENETICS
    68. Malorni, W; Straface, E; Pagano, G; Monti, D; Zatterale, A; Del Principe, D; Deeva, IB; Franceschi, C; Masella, R; Korkina, LG
      Cytoskeleton alterations of erythrocytes from patients with Fanconi's anemia

      FEBS LETTERS
    69. Sala-Trepat, M; Rouillard, D; Escarceller, M; Laquerbe, A; Moustacchi, E; Papadopoulo, D
      Arrest of S-phase progression is impaired in Fanconi anemia cells

      EXPERIMENTAL CELL RESEARCH
    70. Centurion, SA; Kuo, HR; Lambert, WC
      Damage-resistant DNA synthesis in Fanconi anemia cells treated with a DNA gross-linking agent

      EXPERIMENTAL CELL RESEARCH
    71. Grant, SG; Wenger, SL; Latimer, JJ; Thull, D; Burke, LW
      Analysis of genomic instability using multiple assays in a patient with Rothmund-Thomson syndrome

      CLINICAL GENETICS
    72. Moser, MJ; Bigbee, WL; Grant, SG; Emond, MJ; Langlois, RG; Jensen, RH; Oshima, J; Monnat, RJ
      Genetic instability and hematologic disease risk in Werner syndrome patients and heterozygotes

      CANCER RESEARCH
    73. Sieff, CA; Nisbet-Brown, E; Nathan, DG
      Congenital bone marrow failure syndromes

      BRITISH JOURNAL OF HAEMATOLOGY
    74. Ben-Yosef, T; Benvenisty, N
      Hereditary cancer and developmental abnormalities

      BIOLOGY OF THE NEONATE
    75. Papouli, E; Lafon, C; Valette, A; Zdzienicka, MZ; Defais, M; Larminat, F
      Involvement of apoptosis in mitomycin C hypersensitivity of Chinese hamster cell mutants

      BIOCHEMICAL PHARMACOLOGY
    76. Huber, PAJ; Medhurst, AL; Youssoufian, H; Mathew, CG
      Investigation of Fanconi anemia protein interactions by yeast two-hybrid analysis

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    77. Nakamura, A; Matsuura, S; Tauchi, H; Hanada, R; Ohashi, H; Hasegawa, T; Honda, K; Masuno, M; Imaizumi, K; Sugita, K; Ide, T; Komatsu, K
      Four novel mutations of the Fanconi anemia group A gene (FAA) in Japanese patients

      JOURNAL OF HUMAN GENETICS
    78. Laquerbe, A; Sala-Trepat, M; Vives, C; Escarceller, M; Papadopoulo, D
      Molecular spectra of HPRT deletion mutations in circulating T-lymphocytes in Fanconi anemia patients

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    79. Matsumoto, L; Kurek, K; Larocque, K; Gustafson, G; Pires, R; Zhang, J; Tantravahi, U; Suggs, JW
      Biological effects of a bifunctional DNA crosslinker - I. Generation of triradial and quadriradial chromosomes

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    80. Youssoufian, H; Gharibyan, V; Qatanani, M
      Analysis of epitope-tagged forms of the dyskeratosis congenita protein (dyskerin): Identification of a nuclear localization signal

      BLOOD CELLS MOLECULES AND DISEASES
    81. Aker, M; Varadi, G; Slavin, S; Nagler, A
      Fludarabine-based protocol for human umbilical cord blood transplantation in children with fanconi anemia

      JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
    82. Gazda, H
      Congenital bone marrow failure

      INTERNATIONAL JOURNAL OF PEDIATRIC HEMATOLOGY/ONCOLOGY
    83. Kruk, PA; Bohr, VA
      Telomeric length in individuals and cell lines with altered p53 status

      RADIATION ONCOLOGY INVESTIGATIONS
    84. Tachibana, A; Kato, T; Ejima, Y; Yamada, T; Shimizu, T; Yang, LC; Tsunematsu, Y; Sasaki, MS
      The FANCA gene in Japanese Fanconi anemia: Report of eight novel mutationsand analysis of sequence variability

      HUMAN MUTATION
    85. Carreau, M; Alon, N; Bosnoyan-Collins, L; Joenje, H; Buchwald, M
      Drug sensitivity spectra in Fanconi anemia lymphoblastoid cell lines of defined complementation groups

      MUTATION RESEARCH-DNA REPAIR
    86. Friedberg, EC; Meira, LB
      Database of mouse strains carrying targeted mutations in genes affecting cellular responses to DNA damage: version 3

      MUTATION RESEARCH-DNA REPAIR
    87. Sharief, FS; Vojta, PJ; Ropp, PA; Copeland, WC
      Cloning and chromosomal mapping of the human DNA polymerase theta (POLQ), the eighth human DNA polymerase

      GENOMICS
    88. Lensch, MW; Rathbun, RK; Olson, SB; Jones, GR; Bagby, GC
      Selective pressure as an essential force in molecular evolution of myeloidleukemic clones: a view from the window of Fanconi anemia

      LEUKEMIA
    89. Kupfer, G; Naf, D; Garcia-Higuera, I; Wasik, J; Cheng, A; Yamashita, T; Tipping, A; Morgan, N; Mathew, CG; D'Andrea, AD
      A patient-derived mutant form of the Fanconi anemia protein, FANCA, is defective in nuclear accumulation

      EXPERIMENTAL HEMATOLOGY
    90. Carreau, M; Gan, OI; Liu, L; Doedens, M; Dick, JE; Buchwald, M
      Hematopoietic compartment of Fanconi anemia group C null mice contains fewer lineage-negative CD34(+) primitive hematopoietic cells and shows reducedreconstitution ability

      EXPERIMENTAL HEMATOLOGY
    91. Koh, PS; Hughes, GC; Faulkner, GR; Keeble, WW; Bagby, GC
      The Fanconi anemia group C gene product modulates apoptotic responses to tumor necrosis factor-alpha and Fas ligand but does not suppress expression of receptors of the tumor necrosis factor receptor superfamily

      EXPERIMENTAL HEMATOLOGY
    92. Dirksen, U; Moritz, T; Burdach, S; Flasshove, M; Hanenberg, H
      Fanconi anemia and beta c deficiency-associated pulmonary alveolar proteinosis as two hereditary diseases of childhood which are potentially curable by stem cell gene therapy but require different therapeutic approaches

      KLINISCHE PADIATRIE
    93. Alter, BP
      Bone marrow failure syndromes

      CLINICS IN LABORATORY MEDICINE
    94. McLaurin, TM; Bukrey, CD; Lovett, RJ; Mochel, DM
      Management of thrombocytopenia-absent radius (TAR) syndrome

      JOURNAL OF PEDIATRIC ORTHOPAEDICS
    95. Li, L; Peterson, CA; Lu, XY; Wei, P; Legerski, RJ
      Interstrand cross-links induce DNA synthesis in damaged and undamaged plasmids in mammalian cell extracts

      MOLECULAR AND CELLULAR BIOLOGY
    96. de Medeiros, CR; Zanis-Neto, J; Pasquini, R
      Bone marrow transplantation for patients with Fanconi anemia: reduced doses of cyclophosphamide without irradiation as conditioning

      BONE MARROW TRANSPLANTATION
    97. Landau, M; Krafchik, BR
      The diagnostic value of cafe-au-lait macules

      JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY
    98. Clericuzio, CL
      Recognition and management of childhood cancer syndromes: A systems approach

      AMERICAN JOURNAL OF MEDICAL GENETICS
    99. Gripp, KW; Stolle, CA; Celle, L; McDonald-McGinn, DM; Whitaker, LA; Zackai, EH
      TWIST gene mutation in a patient with radial aplasia and craniosynostosis:Further evidence for heterogeneity of Baller-Gerold syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    100. Sanchez, MDE; Cantoni, AC; Alvarez, BM; Cruz-Alcivar, R; Sandoval, SS; Laguna, LG; Vazquez, SF
      Clinical and cytogenetic variability on twelve Fanconi anemia families andits relationship with complementation group assignment

      REVISTA DE INVESTIGACION CLINICA


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Documento generato il 30/10/20 alle ore 05:54:23