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La ricerca find articoli where soggetti phrase all words 'DIGEORGE SYNDROME' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 388 riferimenti
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    1. Lindsay, EA
      Chromosomal microdeletions: Dissecting del22q11 syndrome

      NATURE REVIEWS GENETICS
    2. Van Esch, H; Devriendt, K
      Transcription factor GATA3 and the human HDR syndrome

      CELLULAR AND MOLECULAR LIFE SCIENCES
    3. Chung, MY; Lu, JH; Chien, HP; Hwang, B
      Chromosome 22q11 microdeletion in conotruncal heart defects: Clinical presentation, parental origin and de novo mutations

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    4. De Decker, HP; Lawrenson, JB
      The 22q11.2 deletion: From diversity to a single gene theory

      GENETICS IN MEDICINE
    5. Shaikh, TH; Kurahashi, H; Emanuel, BS
      Evolutionarily conserved low copy repeats (LCRs) in 22q11 mediate deletions, duplications, translocations, and genomic instability: An update and literature review

      GENETICS IN MEDICINE
    6. Driscoll, DA
      Prenatal diagnosis of the 22q11.2 deletion syndrome

      GENETICS IN MEDICINE
    7. Weinzimer, SA
      Endocrine aspects of the 22q11.2 deletion syndrome

      GENETICS IN MEDICINE
    8. McDonald-McGinn, DM; Tonnesen, MK; Laufer-Cahana, A; Finucane, B; Driscoll, DA; Emanuel, BS; Zackai, EH
      Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: Cast a wide FISHing net!

      GENETICS IN MEDICINE
    9. Gerdes, M; Solot, C; Wang, PP; McDonald-McGinn, DM; Zackai, EH
      Taking advantage of early diagnosis: Preschool children with the 22q11.2 deletion

      GENETICS IN MEDICINE
    10. Marino, B; Digilio, MC; Toscano, A; Anaclerio, S; Giannotti, A; Feltri, C; de Ioris, MA; Angioni, A; Dallapiccola, B
      Anatomic patterns of conotruncal defects associated with deletion 22q11

      GENETICS IN MEDICINE
    11. Hokanson, JS; Pierpont, ME; Hirsch, B; Moller, JH
      22q11.2 microdeletions in adults with familial tetralogy of Fallot

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

      GENOME RESEARCH
    13. Hong, R
      The DiGeorge anomaly

      CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY
    14. Ancell, CD; Phipps, J; Young, L
      Thymosin alpha-1

      AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY
    15. Cote, F; Boisvert, FM; Grondin, B; Bazinet, H; Goodyer, CG; Bazett-Jones, DP; Aubry, M
      Alternative promoter usage and splicing of ZNF74 multifinger gene produce protein isoforms with a different repressor activity and nuclear partitioning

      DNA AND CELL BIOLOGY
    16. Garfield, N; Karaplis, AC
      Genetics and animal models of hypoparathyroidism

      TRENDS IN ENDOCRINOLOGY AND METABOLISM
    17. Frober, R; Kohoutek, T; Kahler, C; Beensen, V; Hauschild, R; Schulze, E; Linss, W
      Pulmonary atresia with hypoplastic right ventricle - A clinical embryological study

      FETAL DIAGNOSIS AND THERAPY
    18. Paylor, R; McIlwain, KL; McAninch, R; Nellis, A; Yuva-Paylor, LA; Baldini, A; Lindsay, EA
      Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments

      HUMAN MOLECULAR GENETICS
    19. Funke, B; Epstein, JA; Kochilas, LK; Lu, MM; Pandita, RK; Liao, J; Bauerndistel, R; Schuler, T; Schorle, H; Brown, MC; Adams, J; Morrow, BE
      Mice overexpressing genes from the 22q11 region deleted in velo-cardio-facial syndrome/DiGeorge syndrome have middle and inner ear defects

      HUMAN MOLECULAR GENETICS
    20. Bird, LM
      Cortical dysgenesis and 22q11 deletion

      CLINICAL DYSMORPHOLOGY
    21. Feiner, L; Webber, AL; Brown, CB; Lu, MM; Jia, L; Feinstein, P; Mombaerts, P; Epstein, JA; Raper, JA
      Targeted disruption of semaphorin 3C leads to persistent truncus arteriosus and aortic arch interruption

      DEVELOPMENT
    22. Chung, MY; Lu, JH; Weng, YY; Hwang, BT
      Absence of mutations in human ubiquitin fusion-degradation protein gene intetralogy of Fallot

      JOURNAL OF MOLECULAR MEDICINE-JMM
    23. Van Esch, H; Bilous, RW
      GATA3 and kidney development: why case reports are still important

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    24. Kariyazono, H; Ohno, T; Ihara, K; Igarashi, H; Joh-o, K; Ishikawa, S; Hara, T
      Rapid detection of the 22q11.2 deletion with quantitative real-time PCR

      MOLECULAR AND CELLULAR PROBES
    25. Funke, B; Pandita, RK; Morrow, BE
      Isolation and characterization of a novel gene containing WD40 repeats from the region deleted in velo-cardio-facial/DiGeorge syndrome on chromosome 22q11

      GENOMICS
    26. Trombetti, A; Bottani, A; George, F; Rizzoli, R
      Hypoparathyroidism associated with aneurysm of the left subclavian artery (Kommerell's diverticulum) in an adult patient with a chromosome 22q11.2 deletion

      JOURNAL OF BONE AND MINERAL RESEARCH
    27. Martire, B; Burattini, MG; De Santis, A; Schettini, F; De Mattia, D
      Benign lymphoproliferation syndrome, autoimmune neutropenia and thrombocytopenia in partial Di George syndrome: Efficacy of rh G-CSF and prednisone

      ACTA PAEDIATRICA
    28. McElhinney, DB; Clark, BJ; Weinberg, PM; Kenton, ML; McDonald-McGinn, D; Driscoll, DA; Zackai, EH; Goldmuntz, E
      Association of chromosome 22q11 deletion with isolated anomalies of aorticarch laterality and branching

      JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
    29. Maynard, TM; Sikich, L; Lieberman, JA; LaMantia, AS
      Neural development, cell-cell signaling, and the "two-hit" hypothesis of schizophrenia

      SCHIZOPHRENIA BULLETIN
    30. Bhattacharya, N; Mukherjee, KL; Chettri, MK; Banerjee, T; Bhattacharya, S; Ghosh, A; Bhattacharya, M
      A unique experience with human pre-immune (12 weeks) and hypo-immune (16 weeks) fetal thymus transplant in a vascular subcutaneous axillary fold in patients with advanced cancer: A report of two cases

      EUROPEAN JOURNAL OF GYNAECOLOGICAL ONCOLOGY
    31. Botta, A; Tandoi, C; Fini, G; Calabrese, G; Dallapiccola, B; Novelli, G
      Cloning and characterization of the gene encoding human NPL4, a protein interacting with the ubiquitin fusion-degradation protein (UFD1L)

      GENE
    32. Yin, EZ; Frush, DP; Donnelly, LF; Buckley, RH
      Primary immunodeficiency disorders in pediatric patients: Clinical features and imaging findings

      AMERICAN JOURNAL OF ROENTGENOLOGY
    33. Davies, K; Stiehm, ER; Woo, P; Murray, KJ
      Juvenile idiopathic polyarticular arthritis and IgA deficiency in the 22q11 deletion syndrome

      JOURNAL OF RHEUMATOLOGY
    34. Botham, CA; Jones, GV; Kendall, MD
      Immuno-characterisation of neuroendocrine cells of the rat thymus gland invitro and in vivo

      CELL AND TISSUE RESEARCH
    35. Hall, C; Nelson, DM; Ye, XF; Baker, K; DeCaprio, JA; Seeholzer, S; Lipinski, M; Adams, PD
      HIRA, the human homologue of yeast Hir1p and Hir2p, is a novel cyclin-cdk2substrate whose expression blocks S-phase progression

      MOLECULAR AND CELLULAR BIOLOGY
    36. Yoshida, K; Kuo, F; George, EL; Sharpe, AH; Dutta, A
      Requirement of CDC45 for postimplantation mouse development

      MOLECULAR AND CELLULAR BIOLOGY
    37. Gelb, BD
      Genetic basis of syndromes associated with congenital heart disease

      CURRENT OPINION IN CARDIOLOGY
    38. De Lucia, F; Lorain, S; Scamps, C; Galisson, F; Machold, J; Lipinski, M
      Subnuclear localization and mitotic phosphorylation of HIRA, the human homologue of Saccharomyces cerevisiae transcriptional regulators Hir1p/Hir2p

      BIOCHEMICAL JOURNAL
    39. Lu, JH; Chung, MY; Betau, H; Chien, HP; Lu, JK
      Molecular characterization of tetralogy of Fallot within DiGeorge criticalregion of the chromosome 22

      PEDIATRIC CARDIOLOGY
    40. Duke, C; Chan, KC
      Isolated innominate artery in 22q11 microdeletion

      PEDIATRIC CARDIOLOGY
    41. Mills, AA; Bradley, A
      From mouse to man: generating megabase chromosome rearrangements

      TRENDS IN GENETICS
    42. Lorain, S; Lecluse, Y; Scamps, C; Mattei, MG; Lipinski, M
      Identification of human and mouse HIRA-interacting protein-5 (HIRIP5), twomammalian representatives in a family of phylogenetically conserved proteins with a role in the biogenesis of Fe/S proteins

      BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION
    43. Nakagawa, M; Okuno, M; Okamoto, N; Fujino, H; Kato, H
      Bernard-Soulier syndrome associated with 22q11.2 microdeletion

      AMERICAN JOURNAL OF MEDICAL GENETICS
    44. Aftimos, S; McGaughran, J
      Toriello-Carey syndrome: Case report with additional findings

      AMERICAN JOURNAL OF MEDICAL GENETICS
    45. De Luca, A; Pasini, A; Amati, F; Botta, A; Spalletta, G; Alimenti, S; Caccamo, F; Conti, E; Trakalo, J; Macciardi, F; Dallapiccola, B; Novelli, G
      Association study of a promoter polymorphism of UFD1L gene with schizophrenia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    46. Li-Ling, J
      Connections between Traditional Chinese Medicine and congenital syndromes

      AMERICAN JOURNAL OF MEDICAL GENETICS
    47. Elder, DA; Kaiser-Rogers, K; Aylsworth, AS; Calikoglu, AS
      Type I diabetes mellitus in a patient with chromosome 22q11.2 deletion syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    48. Merscher, S; Funke, B; Epstein, JA; Heyer, J; Puech, A; Lu, MM; Xavier, RJ; Demay, MB; Russell, RG; Factor, S; Tokooya, K; Jore, BS; Lopez, M; Pandita, RK; Lia, M; Carrion, D; Xu, H; Schorle, H; Kobler, JB; Scambler, P; Wynshaw-Boris, A; Skoultchi, AI; Morrow, BE; Kucherlapati, R
      TBX1 is responsible for cardiovascular defects in Velo-Cardio-Facial/DiGeorge syndrome

      CELL
    49. Srivastava, D
      Genetic assembly of the heart: Implications for congenital heart disease

      ANNUAL REVIEW OF PHYSIOLOGY
    50. Munoz, S; Garay, F; Flores, I; Heusser, F; Talesnik, E; Aracena, M; Mellado, C; Mendez, C; Arnaiz, P; Repetto, G
      Clinical heterogeneity of the chromosome 22q11 microdeletion syndrome

      REVISTA MEDICA DE CHILE
    51. McElhinney, DB; Mcdonald-McGinn, D; Zackai, EH; Goldmuntz, E
      Cardiovascular anomalies in patients diagnosed with a chromosome 22q11 deletion beyond 6 months of age

      PEDIATRICS
    52. Morini, F; Cozzi, DA; Ilari, M; Casati, A; Cozzi, F
      Pattern of cardiovascular anomalies associated with esophageal atresia: Support for a caudal pharyngeal arch neurocristopathy

      PEDIATRIC RESEARCH
    53. Jawad, AF; McDonald-McGinn, DM; Zackai, E; Sullivan, KE
      Immunologic features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)

      JOURNAL OF PEDIATRICS
    54. Henwood, J; Pickard, C; Leek, JP; Bennett, CP; Crow, YJ; Thomson, JDR; Ahmed, M; Watterson, KG; Parsons, JM; Roberts, E; Lench, NJ
      A region of homozygosity within 22q11.2 associated with congenital heart disease: recessive DiGeorge/velocardiofacial syndrome?

      JOURNAL OF MEDICAL GENETICS
    55. Brandenburg, VM; Mertens, PR; Block, F; Riehl, J
      DiGeorge syndrome with hypoparathyroidism and cellular immunodeficiency (22q11 chromosome deletion)

      INTERNIST
    56. Pignata, C; Gaetaniello, L; Masci, AM; Frank, J; Christiano, A; Matrecano, E; Racioppi, L
      Human equivalent of the mouse Nude/SCID phenotype: long-term evaluation ofimmunologic reconstitution after bone marrow transplantation

      BLOOD
    57. Eliez, S; Schmitt, JE; White, CD; Wellis, VG; Reiss, AL
      A quantitative MRI study of posterior fossa development in velocardiofacial syndrome

      BIOLOGICAL PSYCHIATRY
    58. Igaki, H; Nakagawa, K; Aoki, Y; Ohtomo, K; Kukimoto, I; Kanda, T
      Characterization of the bi-directional transcriptional control region between the human UFD1L and CDC45L genes

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    59. Edelmann, L; Spiteri, E; Koren, K; Pulijaal, V; Bialer, MG; Shanske, A; Goldberg, R; Morrow, BE
      AT-rich palindromes mediate the constitutional t(11;22) translocation

      AMERICAN JOURNAL OF HUMAN GENETICS
    60. Foster, CB; Choi, EH; Chanock, SJ
      Adenovirus and marrow transplantation in children

      PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE
    61. Gelb, BD
      Recent advances in the understanding of genetic causes of congenital heartdefects

      FRONTIERS IN BIOSCIENCE
    62. McElhinney, DB; Hanley, FL; Stanger, P
      Familial absent pulmonary valve syndrome without deletions of chromosome 22q11

      CARDIOLOGY IN THE YOUNG
    63. Ohta, H; Tokimasa, S; Zou, ZH; Funaki, S; Kurahashi, H; Takahashi, Y; Kimura, M; Matsuoka, R; Horie, M; Hara, J; Shimada, K; Takihara, Y
      Structure and chromosomal localization of the RAE28/HPH1 gene, a human homologue of the polyhomeotic gene

      DNA SEQUENCE
    64. Mateos, MAM; Duenas, BP; Iriondo, M; Krauel, J; Molins, EG
      Clinical and immunological spectrum of partial DiGeorge syndrome

      JOURNAL OF INVESTIGATIONAL ALLERGOLOGY & CLINICAL IMMUNOLOGY
    65. Bergman, A; Blennow, E
      Inv dup(22), del(22)(q11) and r(22) in the father of a child with DiGeorgesyndrome

      EUROPEAN JOURNAL OF HUMAN GENETICS
    66. Shaikh, TH; Kurahashi, H; Saitta, SC; O'Hare, AM; Hu, P; Roe, BA; Driscoll, DA; McDonald-McGinn, DM; Zackai, EH; Budarf, ML; Emanuel, BS
      Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome:genomic organization and deletion endpoint analysis

      HUMAN MOLECULAR GENETICS
    67. Scambler, PJ
      The 22q11 deletion syndromes

      HUMAN MOLECULAR GENETICS
    68. Feinstein, C; Eliez, S
      The velocardiofacial syndrome in psychiatry

      CURRENT OPINION IN PSYCHIATRY
    69. Jiang, XB; Rowitch, DH; Soriano, P; McMahon, AP; Sucov, HM
      Fate of the mammalian cardiac neural crest

      DEVELOPMENT
    70. Yeruham, I; Orgad, U; Avidar, Y
      Congenital thymic aplasia in a Holstein-Israeli female calf

      JOURNAL OF VETERINARY MEDICINE SERIES B-INFECTIOUS DISEASES AND VETERINARYPUBLIC HEALTH
    71. Maldonado-Saldivia, J; Funke, B; Pandita, RK; Schuler, T; Morrow, BE; Schorle, H
      Expression of Cdcrel-1 (Pnutl1), a gene frequently deleted in velo-cardio-facial syndrome/DiGeorge syndrome

      MECHANISMS OF DEVELOPMENT
    72. Kawamura, T; Nimura, I; Hanafusa, M; Fujikawa, R; Okubo, M; Egusa, G; Yamakido, M
      DiGeorge syndrome with Graves' disease: A case report

      ENDOCRINE JOURNAL
    73. Alizad, A; Seward, JB
      Echocardiographic features of genetic diseases: Part 7. Complex genetic disorders

      JOURNAL OF THE AMERICAN SOCIETY OF ECHOCARDIOGRAPHY
    74. Viana, M; Aruoma, OI; Herrera, E; Bonet, B
      Oxidative damage in pregnant diabetic rats and their embryos

      FREE RADICAL BIOLOGY AND MEDICINE
    75. Marcinkowski, M; Bauer, K; Stoltenburg-Didinger, G; Vogel, M; Versmold, H
      Fatal aspergillosis with brain abscesses ln a neonate with digeorge syndrome

      PEDIATRIC INFECTIOUS DISEASE JOURNAL
    76. Lund, J; Chen, F; Hua, A; Roe, B; Budarf, M; Emanuel, BS; Reeves, RH
      Comparative sequence analysis of 634 kb of the mouse chromosome 16 region of conserved synteny with the human velocardiofacial syndrome region on chromosome 22q11.2

      GENOMICS
    77. Perkins, JA; Sie, K; Gray, S
      Presence of 22q11 deletion in postadenoidectomy velopharyngeal insufficiency

      ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY
    78. Haynes, BF; Markert, ML; Sempowski, GD; Patel, DD; Hale, LP
      The role of the thymus in immune reconstitution in aging, bone marrow transplantation, and HIV-1 infection

      ANNUAL REVIEW OF IMMUNOLOGY
    79. Garcia-Garcia, E; Camacho-Alonso, J; Gomez-Rodriguez, MJ; del Castillo, E; Martinez-Aedo, MJ; Lopez-Siguero, JP
      Transient congenital hypoparathyroidism and 22q11 deletion

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    80. Manson, DE; Sikka, S; Reid, B; Roifman, C
      Primary immunodeficiencies: a pictorial immunology primer for radiologists

      PEDIATRIC RADIOLOGY
    81. Marin, MJD; Ruiz, AF; Garcia-Guereta, L; Bartolome, FB; Burgueros, M; Vidal, MDR; Segura, SA; Moreno, F; Bouthelier, RG
      Thyroid function alterations in children with congenital cardiac disease after catheterization with iodinated contrast agents

      REVISTA ESPANOLA DE CARDIOLOGIA
    82. Meyer, HH; Shorter, JG; Seemann, J; Pappin, D; Warren, G
      A complex of mammalian Ufd1 and Npl4 links the AAA-ATPase, p97, to ubiquitin and nuclear transport pathways

      EMBO JOURNAL
    83. Gong, LM; Liu, MY; Jen, J; Yeh, ETH
      GNB1L, a gene deleted in the critical region for DiGeorge syndrome on 22q11, encodes a G-protein beta-subunit-like polypeptide

      BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION
    84. Maschhoff, KL; Baldwin, HS
      Molecular determinants of neural crest migration

      AMERICAN JOURNAL OF MEDICAL GENETICS
    85. Swillen, A; Vogels, A; Devriendt, K; Fryns, JP
      Chromosome 22q11 deletion syndrome: Update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications

      AMERICAN JOURNAL OF MEDICAL GENETICS
    86. Ogilvie, CM; Moore, J; Daker, M; Palferman, S; Docherty, Z
      Chromosome 22q11 deletions are not found in autistic patients identified using strict diagnostic criteria

      AMERICAN JOURNAL OF MEDICAL GENETICS
    87. Tamagaki, A; Shima, M; Tomita, R; Okumura, M; Shibata, M; Morichika, S; Kurahashi, H; Giddings, JC; Yoshioka, A; Yokobayashi, Y
      Segregation of a pure form of spastic paraplegia and NOR insertion into Xq11.2

      AMERICAN JOURNAL OF MEDICAL GENETICS
    88. Maeda, J; Yamagishi, H; Matsuoka, R; Ishihara, J; Tokumura, M; Fukushima, H; Ueda, H; Takahashi, E; Yoshiba, S; Kojima, Y
      Frequent association of 22q11.2 deletion with tetralogy of Fallot

      AMERICAN JOURNAL OF MEDICAL GENETICS
    89. Wenger, SL; Boone, LY; Cummins, JH; Del Vecchio, MA; Bay, CA; Hummel, M; Mowery-Rushton, PA
      Newborn infant with inherited ring and de novo interstitial deletion on homologous chromosome 22s

      AMERICAN JOURNAL OF MEDICAL GENETICS
    90. Loffredo, CA; Ferencz, C; Wilson, PD; Lurie, IW
      Interrupted aortic arch: An epidemiologic study

      TERATOLOGY
    91. Elder, ME
      T-cell immunodeficiencies

      PEDIATRIC CLINICS OF NORTH AMERICA
    92. Mandell, DL
      Head and neck anomalies related to the branchial apparatus

      OTOLARYNGOLOGIC CLINICS OF NORTH AMERICA
    93. Van Esch, H; Groenen, P; Nesbit, MA; Schuffenhauer, S; Lichtner, P; Vanderlinden, G; Harding, B; Beetz, R; Bilous, RW; Holdaway, I; Shaw, NJ; Fryns, JP; Van de Ven, WV; Thakker, RV; Devriendt, K
      GATA3 haplo-insufficiency causes human HDR syndrome

      NATURE
    94. Puech, A; Saint-Jore, B; Merscher, S; Russell, RG; Cherif, D; Sirotkin, H; Xu, H; Factor, S; Kucherlapati, R; Skoultchi, AI
      Normal cardiovascular development in mice deficient for 16 genes in 550 kbof the velocardiofacial/DiGeorge syndrome region

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    95. Lichtner, P; Konig, R; Hasegawa, T; Van Esch, H; Meitinger, T; Schuffenhauer, S
      An HDR (hypoparathyroidism, deafness, renal dysplasia) syndrome locus mapsdistal to the DiGeorge syndrome region on 10p13/14

      JOURNAL OF MEDICAL GENETICS
    96. Solot, CB; Knightly, C; Handler, SD; Gerdes, M; McDonald-McGinn, DM; Moss, E; Wang, P; Cohen, M; Randall, P; Larossa, D; Driscoll, DA; Emanuel, BS; Zackai, EH
      Communication disorders in the 22q11.2 microdeletion syndrome

      JOURNAL OF COMMUNICATION DISORDERS
    97. Morava, E; Czako, M; Melegh, B; Kosztolanyi, G
      Velo-cardio-facial phenotype and deletion of 22q11.2 in Hungarian children

      CLINICAL GENETICS
    98. Bird, LM; Scambler, P
      Cortical dysgenesis in 2 patients with chromosome 22q11 deletion

      CLINICAL GENETICS
    99. Sanchez-Ramon, S; Bartolome, J; Sanchez-Luna, M; Franco, ML; Orera, M
      Polydactyly in 22q11 syndrome: should it be taken into account?

      CLINICAL GENETICS
    100. Pierdominici, M; Marziali, M; Giovannetti, A; Oliva, A; Rosso, R; Marino, B; Digilio, MC; Giannotti, A; Novelli, G; Dallapiccola, B; Aiuti, F; Pandolfi, F
      T cell receptor repertoire and function in patients with DiGeorge syndromeand velocardiofacial syndrome

      CLINICAL AND EXPERIMENTAL IMMUNOLOGY


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Documento generato il 31/10/20 alle ore 16:33:24