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La ricerca find articoli where soggetti phrase all words 'VELOCARDIOFACIAL-SYNDROME' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 138 riferimenti
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    1. Cheour, M; Korpilahti, P; Martynova, O; LAng, AH
      Mismatch negativity and late discriminative negativity in investigating speech perception and learning in children and infants

      AUDIOLOGY AND NEURO-OTOLOGY
    2. 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
    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. Driscoll, DA
      Prenatal diagnosis of the 22q11.2 deletion syndrome

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

      GENETICS IN MEDICINE
    6. 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
    7. 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
    8. 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
    9. 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
    10. 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
    11. Hokanson, JS; Pierpont, ME; Hirsch, B; Moller, JH
      22q11.2 microdeletions in adults with familial tetralogy of Fallot

      GENETICS IN MEDICINE
    12. 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
    13. 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
    14. Niklasson, L; Rasmussen, P; Oskarsdottir, S; Gillberg, C
      Neuropsychiatric disorders in the 22q11 deletion syndrome

      GENETICS IN MEDICINE
    15. Hong, R
      The DiGeorge anomaly

      CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY
    16. 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
    17. Komatsu, H; Kihara, A; Komura, E; Mitsufuji, N; Tsujii, H; Kakita, S; Ikuta, H
      Combined trisomy 9p and Shprintzen syndrome resulting from a paternal t(9;22)

      GENETIC COUNSELING
    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. 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
    20. Lazier, K; Chow, EWC; AbdelMalik, P; Scutt, LE; Weksberg, R; Bassett, AS
      Low platelet count in a 22q11 deletion syndrome subtype of schizophrenia

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

      MODERN PATHOLOGY
    22. 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
    23. 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
    24. 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
    25. 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
    26. Davies, K; Stiehm, ER; Woo, P; Murray, KJ
      Juvenile idiopathic polyarticular arthritis and IgA deficiency in the 22q11 deletion syndrome

      JOURNAL OF RHEUMATOLOGY
    27. 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
    28. Botta, A; Amati, F; Novelli, G
      Causes of the phenotype-genotype dissociation in DiGeorge syndrome: clues from mouse models

      TRENDS IN GENETICS
    29. 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
    30. Nakagawa, M; Okuno, M; Okamoto, N; Fujino, H; Kato, H
      Bernard-Soulier syndrome associated with 22q11.2 microdeletion

      AMERICAN JOURNAL OF MEDICAL GENETICS
    31. 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
    32. 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
    33. 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
    34. 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
    35. Jawad, AF; McDonald-McGinn, DM; Zackai, E; Sullivan, KE
      Immunologic features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)

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

      INTERNIST
    37. Murphy, KC; Owen, MJ
      Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia

      BRITISH JOURNAL OF PSYCHIATRY
    38. Van Amelsvoort, T; Daly, E; Robertson, D; Suckling, J; Ng, V; Critchley, H; Owen, MJ; Henry, J; Murphy, KC; Murphy, DGM
      Structural brain abnormalities associated with deletion at chromosome 22q11 - Quantitative neuroimaging study of adults with velo-cardio-facial syndrome

      BRITISH JOURNAL OF PSYCHIATRY
    39. 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
    40. Kraus, N; Cheour, M
      Speech sound representation in the brain

      AUDIOLOGY AND NEURO-OTOLOGY
    41. Gelb, BD
      Recent advances in the understanding of genetic causes of congenital heartdefects

      FRONTIERS IN BIOSCIENCE
    42. 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
    43. Shprintzen, RJ
      Velo-cardio-facial syndrome: A distinctive behavioral phenotype

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    44. Galili, N; Nayak, S; Epstein, JA; Buck, CA
      Rnf4, a RING protein expressed in the developing nervous and reproductive systems, interacts with gscl, a gene within the DiGeorge critical region

      DEVELOPMENTAL DYNAMICS
    45. 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
    46. Scambler, PJ
      The 22q11 deletion syndromes

      HUMAN MOLECULAR GENETICS
    47. Worthington, S; Turner, A; Elber, J; Andrews, PI
      22q11 deletion and polymicrogyria - cause or coincidence?

      CLINICAL DYSMORPHOLOGY
    48. Perkins, JA; Sie, K; Gray, S
      Presence of 22q11 deletion in postadenoidectomy velopharyngeal insufficiency

      ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY
    49. 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
    50. Maschhoff, KL; Baldwin, HS
      Molecular determinants of neural crest migration

      AMERICAN JOURNAL OF MEDICAL GENETICS
    51. 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
    52. Bassett, AS; Chow, EWC; Weksberg, R
      Chromosomal abnormalities and schizophrenia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    53. 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
    54. 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
    55. 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
    56. Epstein, JA; Buck, CA
      Transcriptional regulation of cardiac development: Implications for congenital heart disease and DiGeorge syndrome

      PEDIATRIC RESEARCH
    57. Shifman, A; Finkelstein, Y; Nachmani, A; Ophir, D
      Speech-aid prostheses for neurogenic velopharyngeal incompetence

      JOURNAL OF PROSTHETIC DENTISTRY
    58. 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
    59. Bird, LM; Scambler, P
      Cortical dysgenesis in 2 patients with chromosome 22q11 deletion

      CLINICAL GENETICS
    60. 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
    61. Atkinson, JC; O'Connell, A; Aframian, D
      Oral manisfestations of primary immunological diseases

      JOURNAL OF THE AMERICAN DENTAL ASSOCIATION
    62. Gelb, BD
      Recent advances in the understanding of genetic causes of congenital heartdefects

      PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE
    63. Cheour, M; Ceponiene, R; Hukki, J; Haapanen, ML; Naatanen, R; Alho, K
      Brain dysfunction in neonates with cleft palate revealed by the mismatch negativity

      CLINICAL NEUROPHYSIOLOGY
    64. Hagerman, RJ
      Psychopharmacological interventions in fragile X syndrome, fetal alcohol syndrome, Prader-Willi syndrome, Angelman syndrome, Smith-Magenis syndrome, and velocardiofacial syndrome

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    65. Sullivan, KE; McDonald-McGinn, D; Driscoll, DA; Emanuel, BS; Zackai, EH; Jawad, AF
      Longitudinal analysis of lymphocyte function and numbers in the first yearof life in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)

      CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY
    66. Urnovitz, HB; Tuite, JJ; Higashida, JM; Murphy, WH
      RNAs in the sera of Persian Gulf War veterans have segments homologous to chromosome 22q11.2

      CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY
    67. Carneol, SO; Marks, SM; Weik, LA
      The speech-language pathologist: Key role in the diagnosis of velocardiofacial syndrome

      AMERICAN JOURNAL OF SPEECH-LANGUAGE PATHOLOGY
    68. Digilio, MC; Pacifico, C; Tieri, L; Marino, B; Giannotti, A; Dallapiccola, B
      Audiological findings in patients with microdeletion 22q11 (di George/velocardiofacial syndrome)

      BRITISH JOURNAL OF AUDIOLOGY
    69. Pollard, ME; Cushing, MV; Ogden, JA
      Musculoskeletal abnormalities in velocardiofacial syndrome

      JOURNAL OF PEDIATRIC ORTHOPAEDICS
    70. Scherer, NJ; D'Antonio, LL; Kalbfleisch, JH
      Early speech and language development in children with velocardiofacial syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    71. Cohen, E; Chow, EWC; Weksberg, R; Bassett, AS
      Phenotype of adults with the 22q11 deletion syndrome: A review

      AMERICAN JOURNAL OF MEDICAL GENETICS
    72. McQuade, L; Christodoulou, J; Budarf, M; Sachdev, R; Wilson, M; Emanuel, B; Colley, A
      Patient with a 22q11.2 deletion with no overlap of the minimal DiGeorge syndrome critical region (MDGCR)

      AMERICAN JOURNAL OF MEDICAL GENETICS
    73. Gerdes, M; Solot, C; Wang, PP; Moss, E; LaRossa, D; Randall, P; Goldmuntz, E; Clark, BJ; Driscoll, DA; Jawad, A; Emanuel, BS; McDonald-McGinn, DM; Batshaw, ML; Zackai, EH
      Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion

      AMERICAN JOURNAL OF MEDICAL GENETICS
    74. Lu, JH; Chung, MY; Hwang, BT; Chien, HP
      Prevalence and parental origin in tetralogy of Fallot associated with chromosome 22q11 microdeletion

      PEDIATRICS
    75. Moss, EM; Batshaw, ML; Solot, CB; Gerdes, M; McDonald-McGinn, DM; Driscoll, DA; Emanuel, BS; Zackai, EH; Wang, PP
      Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern

      JOURNAL OF PEDIATRICS
    76. Sugama, S; Namihira, T; Matsuoka, R; Taira, N; Eto, Y; Maekawa, K
      Psychiatric inpatients and chromosome deletions within 22q11.2

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    77. Digilio, MC; Marino, B; Bagolan, P; Giannotti, A; Dallapiccola, B
      Microdeletion 22q11 and oesophageal atresia

      JOURNAL OF MEDICAL GENETICS
    78. Liling, J; Cross, I; Burn, J; Daniel, CP; Tawn, EJ; Parker, L
      Frequency and predictive value of 22q11 deletion

      JOURNAL OF MEDICAL GENETICS
    79. Witt, P; Cohen, D; Grames, LM; Marsh, J
      Sphincter pharyngoplasty for the surgical management of speech dysfunctionassociated with velocardiofacial syndrome

      BRITISH JOURNAL OF PLASTIC SURGERY
    80. Bassett, AS; Chow, EWC
      22q11 deletion syndrome: A genetic subtype of schizophrenia

      BIOLOGICAL PSYCHIATRY
    81. Chow, EWC; Mikulis, DJ; Zipursky, RB; Scutt, LE; Weksberg, R; Bassett, AS
      Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia

      BIOLOGICAL PSYCHIATRY
    82. CREWTHER SG; KIELY PM; KOK LL; CREWTHER DP
      ANOMALIES OF GENETIC DEVELOPMENT AS PREDICTORS OF OCULO-VISUAL ABNORMALITIES IN VELO-CARDIO-FACIAL SYNDROME

      Optometry and vision science
    83. WORTHINGTON S; BOWER C; HARROP K; LOH J; WALPOLE I
      22Q11 DELETIONS IN PATIENTS WITH CONOTRUNCAL HEART-DEFECTS

      Journal of paediatrics and child health
    84. CHEOUR M; HAAPANEN ML; CEPONIENE R; HUKKI J; RANTA R; NAATANEN R
      MISMATCH NEGATIVITY (MMN) AS AN INDEX OF AUDITORY SENSORY MEMORY DEFICIT IN CLEFT-PALATE AND CATCH SYNDROME CHILDREN

      NeuroReport
    85. CHUDLEY AE; GUTIERREZ E; JOCELYN LJ; CHODIRKER BN
      OUTCOMES OF GENETIC EVALUATION IN CHILDREN WITH PERVASIVE DEVELOPMENTAL DISORDER

      Journal of developmental and behavioral pediatrics
    86. WANG PP; SOLOT C; MOSS EM; GERDES M; MCDONALDMCGINN DM; DRISCOLL DA; EMANUEL BS; ZACKAI EH
      DEVELOPMENTAL PRESENTATION OF 22Q11.2 DELETION (DIGEORGE VELOCARDIOFACIAL-SYNDROME)/

      Journal of developmental and behavioral pediatrics
    87. VANTRAPPEN G; ROMMEL N; CREMERS CWRJ; DEVRIENDT K; FRIJNS JP
      THE VELO-CARDIO-FACIAL SYNDROME - THE OTORHINOLARYNGEAL MANIFESTATIONS AND IMPLICATIONS

      International journal of pediatric otorhinolaryngology
    88. BASSETT AS; HODGKINSON K; CHOW EWC; CORREIA S; SCUTT LE; WEKSBERG R
      22Q11 DELETION SYNDROME IN ADULTS WITH SCHIZOPHRENIA

      American journal of medical genetics
    89. YAN WL; JACOBSEN LK; KRASNERWICH DM; GUAN XY; LENANE MC; PAUL SP; DALWADI HN; ZHANG HG; LONG RT; KUMRA S; MARTIN BM; SCAMBLER PJ; TRENT JM; SIDRANSKY E; GINNS EI; RAPOPORT JL
      CHROMOSOME 22Q11.2 INTERSTITIAL DELETIONS AMONG CHILDHOOD-ONSET SCHIZOPHRENICS AND MULTIDIMENSIONALLY IMPAIRED

      American journal of medical genetics
    90. HATCHWELL E; LONG F; WILDE J; CROLLA J; TEMPLE K
      MOLECULAR CONFIRMATION OF GERM-LINE MOSAICISM FOR A SUBMICROSCOPIC DELETION OF CHROMOSOME 22Q11

      American journal of medical genetics
    91. SULLIVAN KE; JAWAD AF; RANDALL P; DRISCOLL DA; EMANUEL BS; MCDONALDMCGINN DM; ZACKAI EH
      LACK OF CORRELATION BETWEEN IMPAIRED T-CELL PRODUCTION, IMMUNODEFICIENCY, AND OTHER PHENOTYPIC FEATURES IN CHROMOSOME 22Q11.2 DELETION SYNDROMES (DIGEORGE-SYNDROME VELOCARDIOFACIAL SYNDROME)

      Clinical immunology and immunopathology
    92. FRAULIN FOG; VALNICEK SM; ZUKER RM
      DECREASING THE PERIOPERATIVE COMPLICATIONS ASSOCIATED WITH THE SUPERIOR PHARYNGEAL FLAP OPERATION

      Plastic and reconstructive surgery
    93. WEINZIMER SA; MCDONALDMCGINN DM; DRISCOLL DA; EMANUEL BS; ZACKAI EH; MOSHANG T
      GROWTH-HORMONE DEFICIENCY IN PATIENTS WITH A 22Q11.2 DELETION - EXPANDING THE PHENOTYPE

      Pediatrics
    94. SIE KCY; TAMPAKOPOULOU DA; DESERRES LM; GRUSS JS; EBLEN LE; YONICK T
      SPHINCTER PHARYNGOPLASTY - SPEECH OUTCOME AND COMPLICATIONS

      The Laryngoscope
    95. SARAIVA JM; MATOSO E; MARQUES I
      ABSENCE OF A DEL(22Q11) IN A PATIENT WITH THE 3C (CRANIOCEREBELLOCARDIAC) SYNDROME

      Journal of Medical Genetics
    96. VERLOES A; CURRY C; JAMAR M; HERENS C; OLAGUE P; MARKS J; SARDA P; BLANCHET P
      JUVENILE RHEUMATOID-ARTHRITIS AND DEL(22Q11) SYNDROME - A NONRANDOM ASSOCIATION

      Journal of Medical Genetics
    97. DEVRIENDT K; SWILLEN A; FRYNS JP
      DELETION IN CHROMOSOME REGION 22Q11 IN A CHILD WITH CHARGE ASSOCIATION

      Clinical genetics
    98. KITANO I; PARK S; KATO K; NITTA N; TAKATO T; SUSAMI T
      CRANIOFACIAL MORPHOLOGY OF CONOTRUNCAL ANOMALY FACE SYNDROME

      The Cleft palate-craniofacial journal
    99. KRUGMAN ME; BRANTZAWADSKI M
      MAGNETIC-RESONANCE ANGIOPLASTY FOR PREPHARYNGOPLASTY ASSESSMENT IN VELOCARDIOFACIAL SYNDROME

      The Cleft palate-craniofacial journal
    100. ABEL HP; OLEARY DJ
      OPTOMETRIC FINDINGS IN VELOCARDIOFACIAL SYNDROME

      Optometry and vision science


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 20/02/20 alle ore 00:29:04