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La ricerca find articoli where soggetti phrase all words 'CARDIO-FACIAL SYNDROME' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 369 riferimenti
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    1. Bailey, JA; Yavor, AM; Viggiano, L; Misceo, D; Horvath, JE; Archidiacono, N; Schwartz, S; Rocchi, M; Eichler, EE
      Human-specific duplication and mosaic transcripts: The recent paralogous structure of chromosome 22

      AMERICAN JOURNAL OF HUMAN GENETICS
    2. Bray, NJ; Owen, MJ
      Searching for schizophrenia genes

      TRENDS IN MOLECULAR MEDICINE
    3. Lindsay, EA
      Chromosomal microdeletions: Dissecting del22q11 syndrome

      NATURE REVIEWS GENETICS
    4. Bearden, CE; Woodin, MF; Wang, PP; Moss, E; McDonald-McGinn, D; Zackai, E; Emannuel, B; Cannon, TD
      The neurocognitive phenotype of the 22Q11.2 deletion syndrome: Selective deficit in visual-spatial memory

      JOURNAL OF CLINICAL AND EXPERIMENTAL NEUROPSYCHOLOGY
    5. Saleem, Q; Dash, D; Gandhi, C; Kishore, A; Benegal, V; Sherrin, T; Mukherjee, O; Jain, S; Brahmachari, SK
      Association of CAG repeat loci on chromosome 22 with schizophrenia and bipolar disorder

      MOLECULAR PSYCHIATRY
    6. Black, JL; Krahn, LE; Jalal, SM
      Voltage-gated calcium channel gamma 2 subunit gene is not deleted in velo-cardio-facial syndrome

      MOLECULAR PSYCHIATRY
    7. Saito, T; Guan, F; Papolos, DF; Rajouria, N; Fann, CSJ; Lachman, HM
      Polymorphism in SNAP29 gene promoter region associated with schizophrenia

      MOLECULAR PSYCHIATRY
    8. 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
    9. De Decker, HP; Lawrenson, JB
      The 22q11.2 deletion: From diversity to a single gene theory

      GENETICS IN MEDICINE
    10. 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
    11. Driscoll, DA
      Prenatal diagnosis of the 22q11.2 deletion syndrome

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

      GENETICS IN MEDICINE
    13. Digilio, MC; Marino, B; Cappa, M; Cambiaso, P; Giannotti, A; Dallapiccola, B
      Auxological evaluation in patients with DiGeorge/velocardiofacial syndrome(deletion 22q11.2 syndrome)

      GENETICS IN MEDICINE
    14. Woodin, M; Wang, PP; Aleman, D; McDonald-McGinn, D; Zackai, E; Moss, E
      Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion

      GENETICS IN MEDICINE
    15. 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
    16. Eliez, S; Blasey, CM; Menon, V; White, CD; Schmitt, JE; Reiss, AL
      Functional brain imaging study of mathematical reasoning abilities in velocardiofacial syndrome (del22q11.2)

      GENETICS IN MEDICINE
    17. Momma, K; Takao, A; Matsuoka, R; Imai, Y; Muto, A; Osawa, M; Takayama, M
      Tetralogy of Fallot associated with chromosome 22q11.2 deletion in adolescents and young adults

      GENETICS IN MEDICINE
    18. Solot, CB; Gerdes, M; Kirschner, RE; McDonald-McGinn, DM; Moss, E; Woodin, M; Aleman, D; Zackai, EH; Wang, P
      Communication issues in 22q11.2 deletion syndrome: Children at risk

      GENETICS IN MEDICINE
    19. Scherer, NJ; D'Antonio, LL; Rodgers, JR
      Profiles of communication disorder in children with velocardiofacial syndrome: Comparison to children with Down syndrome

      GENETICS IN MEDICINE
    20. Niklasson, L; Rasmussen, P; Oskarsdottir, S; Gillberg, C
      Neuropsychiatric disorders in the 22q11 deletion syndrome

      GENETICS IN MEDICINE
    21. Edelmann, L; Stankiewicz, P; Spiteri, E; Pandita, RK; Shaffer, L; Lupski, J; Morrow, BE
      Two function copies of the DGCR6 gene are present on human chromosome 22q11 due to a duplication of an ancestral locus

      GENOME RESEARCH
    22. Hong, R
      The DiGeorge anomaly

      CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY
    23. Jerome, LA; Papaioannou, VE
      DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

      NATURE GENETICS
    24. D'Antonio, LL; Scherer, NJ; Miller, LL; Kalbfleisch, JH; Bartley, JA
      Analysis of speech characteristics in children with velocardiofacial syndrome (VCFS) and children with phenotypic overlap without VCFS

      CLEFT PALATE-CRANIOFACIAL JOURNAL
    25. Cuneo, BF
      22q11.2 deletion syndrome: DiGeorge, velocardiofacial, and conotruncal anomaly face syndromes

      CURRENT OPINION IN PEDIATRICS
    26. Van Lierde, KM; Van Borsel, J; Van Cauwenberge, P; Callewaert, S
      Speech patterns in children with velo-cardio-facial syndrome - Two case studies

      FOLIA PHONIATRICA ET LOGOPAEDICA
    27. 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
    28. 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
    29. Catalano, M
      Functionally gene-linked polymorphic regions and genetically controlled neurotransmitters metabolism

      EUROPEAN NEUROPSYCHOPHARMACOLOGY
    30. Takase, K; Ohtsuki, T; Migita, O; Toru, M; Inada, T; Yamakawa-Kobayashi, K; Arinami, T
      Association of ZNF74 gene genotypes with age-at-onset of schizophrenia

      SCHIZOPHRENIA RESEARCH
    31. Arinami, T; Ohtsuki, T; Takase, K; Shimizu, H; Yoshikawa, T; Horigome, H; Nakayama, J; Toru, M
      Screening for 22q11 deletions in a schizophrenia population

      SCHIZOPHRENIA RESEARCH
    32. Kapur, RP
      Practicing pediatric pathology without a microscope

      MODERN PATHOLOGY
    33. Moldavsky, M; Lev, D; Lerman-Sagie, T
      Behavioral phenotypes of genetic syndromes: A reference guide for psychiatrists

      JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
    34. Gothelf, D; Lombroso, PJ
      Genetics of childhood disorders: XXV. Velocardiofacial syndrome

      JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
    35. Hodgkinson, KA; Murphy, J; O'Neill, S; Brzustowicz, L; Bassett, AS
      Genetic counselling for schizophrenia in the era of molecular genetics

      CANADIAN JOURNAL OF PSYCHIATRY-REVUE CANADIENNE DE PSYCHIATRIE
    36. Bassett, AS; Chow, EWC; Waterworth, DM; Brzustowicz, L
      Genetic insights into schizophrenia

      CANADIAN JOURNAL OF PSYCHIATRY-REVUE CANADIENNE DE PSYCHIATRIE
    37. Bassett, AS; Chow, EWC; O'Neill, S; Brzustowicz, LM
      Genetic insights into the neurodevelopmental hypothesis of schizophrenia

      SCHIZOPHRENIA BULLETIN
    38. Maynard, TM; Sikich, L; Lieberman, JA; LaMantia, AS
      Neural development, cell-cell signaling, and the "two-hit" hypothesis of schizophrenia

      SCHIZOPHRENIA BULLETIN
    39. Fokstuen, S; Vrticka, K; Riegel, M; Da Silva, V; Baumer, A; Schinzel, A
      Velofacial hypoplasia (Sedlackova syndrome): a variant of velocardiofacial(Shprintzen) syndrome and part of the phenotypical spectrum of del 22q11.2

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

      JOURNAL OF RHEUMATOLOGY
    41. Liou, YJ; Tsai, SJ; Hong, CJ; Wang, YC; Lai, IC
      Association analysis of a functional catechol-O-methyltransferase gene polymorphism in schizophrenic patients in Taiwan

      NEUROPSYCHOBIOLOGY
    42. Gelb, BD
      Genetic basis of syndromes associated with congenital heart disease

      CURRENT OPINION IN CARDIOLOGY
    43. 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
    44. Botta, A; Amati, F; Novelli, G
      Causes of the phenotype-genotype dissociation in DiGeorge syndrome: clues from mouse models

      TRENDS IN GENETICS
    45. de Chaldee, M; Corbex, M; Campion, D; Jay, M; Samolyk, D; Petit, M; Thibaut, F; Laurent, C; Mallet, J
      No evidence for linkage between COMT and schizophrenia in a French population

      PSYCHIATRY RESEARCH
    46. Schulze, BRB; Tariverdian, G; Komposch, G; Stellzig, A
      Misclassification risk of patients with bilateral cleft lip and palate andmanifestations of median facial dysplasia: A new variant of del(22q11.2) syndrome?

      AMERICAN JOURNAL OF MEDICAL GENETICS
    47. Nakagawa, M; Okuno, M; Okamoto, N; Fujino, H; Kato, H
      Bernard-Soulier syndrome associated with 22q11.2 microdeletion

      AMERICAN JOURNAL OF MEDICAL GENETICS
    48. Scutt, LE; Chow, EWC; Weksberg, R; Honer, WG; Bassett, AS
      Patterns of dysmorphic features in schizophrenia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    49. Cai, GQ; Li, T; Deng, D; Zhao, JH; Hu, X; Murray, RM; Liu, XH; Sham, PC; Collier, DA
      Affected sibling pair linkage analysis of qualitative and quantitative traits for schizophrenia on chromosome 22 in a Chinese population

      AMERICAN JOURNAL OF MEDICAL GENETICS
    50. Dobrusin, M; Corbex, M; Kremer, I; Murad, I; Muhaheed, M; Bannoura, I; Muller, DJ; Schulze, TG; Reshef, A; Blanaru, M; Gathas, S; Rietschel, M; Belmaker, RH; Maier, W; Ebstein, RP
      No evidence for linkage by transmission disequilibrium test analysis of microsatellite marker D22S278 and schizophrenia in a Palestinian Arab and in a German population

      AMERICAN JOURNAL OF MEDICAL GENETICS
    51. Arnold, PD; Siegel-Bartelt, J; Cytrynbaum, C; Teshima, I; Schachar, R
      Velo-cardio-facial syndrome: Implications of microdeletion 22q11 for schizophrenia and mood disorders

      AMERICAN JOURNAL OF MEDICAL GENETICS
    52. Gogos, JA; Karayiorgou, M
      "Targeting" schizophrenia in mice

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

      AMERICAN JOURNAL OF MEDICAL GENETICS
    54. Coppola, G; Sciscio, N; Russo, F; Caliendo, G; Pascotto, A
      Benign idiopathic partial seizures in the velocardiofacial syndrome: Report of two cases

      AMERICAN JOURNAL OF MEDICAL GENETICS
    55. Guyot, L; Dubuc, M; Pujol, J; Dutour, O; Philip, N
      Craniofacial anthropometric analysis in patients with 22q11 microdeletion

      AMERICAN JOURNAL OF MEDICAL GENETICS
    56. Graf, WD; Unis, AS; Yates, CM; Sulzbacher, S; Dinulos, MB; Jack, RM; Dugaw, KA; Paddock, MN; Parson, WW
      Catecholamines in patients with 22q11.2 deletion syndrome and the low-activity COMT polymorphism

      NEUROLOGY
    57. Taddei, I; Morishima, M; Huynh, T; Lindsay, EA
      Genetic factors are major determinants of phenotypic variability in a mouse model of the DiGeorge/deI22q11 syndromes

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    58. Jawad, AF; McDonald-McGinn, DM; Zackai, E; Sullivan, KE
      Immunologic features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)

      JOURNAL OF PEDIATRICS
    59. 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
    60. Waibler, Z; Schafer, A; Starzinski-Powitz, A
      mARVCF cellular localisation and binding to cadherins is influenced by thecellular context but not by alternative splicing

      JOURNAL OF CELL SCIENCE
    61. Xu, X; Li, WEI; Huang, GY; Meyer, R; Chen, T; Luo, Y; Thomas, MP; Radice, GL; Lo, CW
      Modulation of mouse neural crest cell motility by N-cadherin and connexin 43 gap junctions

      JOURNAL OF CELL BIOLOGY
    62. Kates, WR; Burnette, CP; Jabs, EW; Rutberg, J; Murphy, AM; Grados, M; Geraghty, M; Kaufmann, WE; Pearlson, GD
      Regional cortical white matter reductions in velocardiofacial syndrome: A volumetric MRI analysis

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

      BIOLOGICAL PSYCHIATRY
    64. Eliez, S; Antonarakis, SE; Morris, MA; Dahoun, SP; Reiss, AL
      Parental origin of the deletion 22q11.2 and brain development in velocardiofacial syndrome - A preliminary study

      ARCHIVES OF GENERAL PSYCHIATRY
    65. Eliez, S; Blasey, CM; Schmitt, EJ; White, CD; Hu, D; Reiss, AL
      Velocardiofacial syndrome: Are structural changes in the temporal and mesial temporal regions related to schizophrenia?

      AMERICAN JOURNAL OF PSYCHIATRY
    66. 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
    67. Schwab, SG; Hallmayer, J; Albus, M; Lerer, B; Eckstein, GN; Borrmann, M; Segman, RH; Hanses, C; Freymann, J; Yakir, A; Trixler, M; Falkai, P; Rietschel, M; Maier, W; Wildenauer, DB
      A genome-wide autosomal screen for schizophrenia susceptibility loci in 71families with affected siblings: support for loci on chromosome 10p and 6

      MOLECULAR PSYCHIATRY
    68. Li, T; Ball, D; Zhao, J; Murray, RM; Liu, X; Sham, PC; Collier, DA
      Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11

      MOLECULAR PSYCHIATRY
    69. Gelb, BD
      Recent advances in the understanding of genetic causes of congenital heartdefects

      FRONTIERS IN BIOSCIENCE
    70. Ji, YG; Eichler, EE; Schwartz, S; Nicholls, RD
      Structure of chromosomal duplicons and their role in mediating human genomic disorders

      GENOME RESEARCH
    71. Balda, MS; Matter, K
      Transmembrane proteins of tight junctions

      SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY
    72. Reiss, AL; Eliez, S; Schmitt, JE; Patwardhan, A; Haberecht, M
      Brain imaging in neurogenetic conditions: Realizing the potential of behavioral neurogenetics research

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    73. Shprintzen, RJ
      Velo-cardio-facial syndrome: A distinctive behavioral phenotype

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    74. Greenberg, IS; Fifer, RC
      Evidence that the association between hypernasality and 22q11 deletion syndrome still goes undetected: A case study

      AMERICAN JOURNAL OF SPEECH-LANGUAGE PATHOLOGY
    75. 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
    76. Mateos, MAM; Duenas, BP; Iriondo, M; Krauel, J; Molins, EG
      Clinical and immunological spectrum of partial DiGeorge syndrome

      JOURNAL OF INVESTIGATIONAL ALLERGOLOGY & CLINICAL IMMUNOLOGY
    77. Eliez, S; Palacio-Espasa, F; Spira, A; Lacroix, M; Pont, C; Luthi, F; Robert-Tissot, C; Feinstein, C; Schorderet, DF; Antonarakis, SE; Cramer, B
      Young children with Velo-Cardio-Facial syndrome (CATCH-22). Psychoiogical and language phenotypes

      EUROPEAN CHILD & ADOLESCENT PSYCHIATRY
    78. 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
    79. Stoltenberg, SF; Burmeister, M
      Recent progress in psychiatric genetics - some hope but no hype

      HUMAN MOLECULAR GENETICS
    80. 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
    81. Scambler, PJ
      The 22q11 deletion syndromes

      HUMAN MOLECULAR GENETICS
    82. Guion-Almeida, ML; Zechi-Ceide, RM; Richieri-Costa, A
      Cleft lip/palate, abnormal ears, ectrodactyly, congenital heart defect, and growth retardation: definition of the acro-cardio-facial syndrome

      CLINICAL DYSMORPHOLOGY
    83. Worthington, S; Turner, A; Elber, J; Andrews, PI
      22q11 deletion and polymicrogyria - cause or coincidence?

      CLINICAL DYSMORPHOLOGY
    84. Bhagwagar, Z; Mawson, D
      Velo-cardio-facial (Shprintzen's) Syndrome, violence and schizophrenia

      JOURNAL OF FORENSIC PSYCHIATRY
    85. Feinstein, C; Eliez, S
      The velocardiofacial syndrome in psychiatry

      CURRENT OPINION IN PSYCHIATRY
    86. Deb, S; Weston, SN
      Psychiatric illness and mental retardation

      CURRENT OPINION IN PSYCHIATRY
    87. 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
    88. Alizad, A; Seward, JB
      Echocardiographic features of genetic diseases: Part 7. Complex genetic disorders

      JOURNAL OF THE AMERICAN SOCIETY OF ECHOCARDIOGRAPHY
    89. Schwer, H; Liu, LQ; Zhou, LM; Little, MT; Pan, Z; Hetherington, CJ; Zhang, DE
      Cloning and characterization of a novel human ubiquitin-specific protease,a homologue of murine UBP43 (Usp18)

      GENOMICS
    90. Duke, SG; McGuirt, WF; Jewett, T; Fasano, MB
      Velocardiofacial syndrome - Incidence of immune cytopenias

      ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY
    91. Sugama, S; Bingham, PM; Wang, PP; Moss, EM; Kobayashi, H; Eto, Y
      Morphometry of the head of the caudate nucleus in patients with velocardiofacial syndrome (del 22q11.2)

      ACTA PAEDIATRICA
    92. Havkin, N; Tatum, SA; Sphrintzen, RJ
      Velopharyngeal insufficiency and articulation impairment in velo-cardio-facial syndrome: the influence of adenoids on phonemic development

      INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY
    93. 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
    94. Riley, BP; McGuffin, P
      Linkage and associated studies of schizophrenia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    95. Bassett, AS; Chow, EWC; Weksberg, R
      Chromosomal abnormalities and schizophrenia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    96. 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
    97. Kawame, H; Kurosawa, K; Akatsuka, A; Ochiai, Y; Mizuno, K
      Polymicrogyria is an uncommon manifestation in 22q11.2 deletion syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    98. Berend, SA; Spikes, AS; Kashork, CD; Wu, JM; Daw, SC; Scambler, PJ; Shaffer, LG
      Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci

      AMERICAN JOURNAL OF MEDICAL GENETICS
    99. Shaffer, LG; Lupski, JR
      Molecular mechanisms for constitutional chromosomal rearrangements in humans

      ANNUAL REVIEW OF GENETICS
    100. Hultman, CS; Riski, JE; Cohen, SR; Burstein, FD; Boydston, WR; Hudgins, RJ; Grattan-Smith, D; Uhas, K; Simms, C
      Chiari malformation, cervical spine anomalies, and neurologic deficits in velocardiofacial syndrome

      PLASTIC AND RECONSTRUCTIVE SURGERY


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Documento generato il 28/02/20 alle ore 14:01:00