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    1. Itin, PH; Keseru, B; Hauser, V
      Syndactyly/brachyphalangy and nail dysplasias as marker lesions for sclerosteosis

      DERMATOLOGY
    2. Hoffman, HM; Bastian, JF; Bird, LM
      Humoral immunodeficiency with facial dysmorphology and limb anomalies: a new syndrome

      CLINICAL DYSMORPHOLOGY
    3. Berg, C; Geipel, A; Germer, U; Pertersen-Hansen, A; Koch-Dorfler, M; Gembruch, U
      Prenatal detection of Fraser syndrome without cryptophthalmos: case reportand review of the literature

      ULTRASOUND IN OBSTETRICS & GYNECOLOGY
    4. Dar, P; Sachs, GS; Carter, SM; Ferreira, JC; Nitowsky, HM; Gross, SJ
      Prenatal diagnosis of Bardet-Biedl syndrome by targeted second-trimester sonography

      ULTRASOUND IN OBSTETRICS & GYNECOLOGY
    5. Montero, JA; Ganan, Y; Macias, D; Rodriguez-Leon, J; Sanz-Ezquerro, JJ; Merino, R; Chimal-Monroy, J; Nieto, MA; Hurle, JM
      Role of FGFs in the control of programmed cell death during limb development

      DEVELOPMENT
    6. Greuse, M; Coessens, BC
      Congenital syndactyly: Defatting facilitates closure without skin graft

      JOURNAL OF HAND SURGERY-AMERICAN VOLUME
    7. Kantaputra, PN; Eiumtrakul, P; Matin, T; Opastirakul, S; Visrutaratna, P; Mevate, U
      Cryptophthalmos, dental and oral abnormalities, and brachymesophalangy of second toes: New syndrome or Fraser syndrome?

      AMERICAN JOURNAL OF MEDICAL GENETICS
    8. Ghadami, M; Majidzadeh-A, K; Haerian, BS; Damavandi, E; Yamada, K; Pasallar, P; Najafi, MT; Nishimura, G; Tomita, HA; Yoshiura, KI; Niikawa, N
      Confirmation of genetic homogeneity of syndactyly type 1 in an Iranian family

      AMERICAN JOURNAL OF MEDICAL GENETICS
    9. Senecky, Y; Halpern, GJ; Inbar, D; Attias, J; Shohat, M
      Ectodermal dysplasia, ectrodactyly and macular dystrophy (EEM syndrome) insiblings

      AMERICAN JOURNAL OF MEDICAL GENETICS
    10. Arteaga-Solis, E; Gayraud, B; Lee, SY; Shum, L; Sakai, L; Ramirez, F
      Regulation of limb patterning by extracellular microfibrils

      JOURNAL OF CELL BIOLOGY
    11. Al-Qattan, MM
      Classification of hand anomalies in Poland's syndrome

      BRITISH JOURNAL OF PLASTIC SURGERY
    12. Bianca, S; Caruso-Nicoletti, M; Volti, GL; Mancuso, M; Volti, SL
      Syndrome of renal, genital and feet malformations

      ANNALES DE GENETIQUE
    13. Gripp, KW; Zackai, EH; Stolle, CA
      Mutations in the human TWIST gene

      HUMAN MUTATION
    14. Seven, M; Yuksel, A; Ozkilic, A; Elcioglu, N
      A variant of Cenani-Lenz type syndactyly

      GENETIC COUNSELING
    15. Kajantie, E; Pirinen, S; Tommiska, V; Kaitila, I
      A syndrome with midface asymmetry, defective modelling of the skeleton, catch-up growth and truncal obesity

      CLINICAL DYSMORPHOLOGY
    16. Baralle, D; Firth, H
      A case of the new overgrowth syndrome - macrocephaly with cutis marmorata,haemangioma and syndactyly

      CLINICAL DYSMORPHOLOGY
    17. Tercan, M; Yakinci, C; Kutlu, O; Demir, C; Durmaz, Y
      Proteus syndrome: a case report and review of the literature

      EUROPEAN JOURNAL OF PLASTIC SURGERY
    18. Markal, N; Velidedeoglu, H; Torkut, A; Kucukcelebi, A
      Abortive cryptophthalmos and cup ear deformity (Fraser syndrome): case report and literature review

      EUROPEAN JOURNAL OF PLASTIC SURGERY
    19. Karacalar, A; Guner, H
      A new technique for the correction of syndactyly of the toes

      EUROPEAN JOURNAL OF PLASTIC SURGERY
    20. Clarke, JC; Becker, EJ; Salonen, DC
      Answer to case of the month #76 - Amniotic band syndrome

      CANADIAN ASSOCIATION OF RADIOLOGISTS JOURNAL-JOURNAL DE L ASSOCIATION CANADIENNE DES RADIOLOGISTES
    21. McCarroll, HR
      Congenital anomalies: A 25-year overview

      JOURNAL OF HAND SURGERY-AMERICAN VOLUME
    22. Stewart, S; Yi, S; Kassabian, G; Mayo, M; Sank, A; Shuler, C
      Changes in expression of the lysosomal membrane glycoprotein, LAMP-1 in interdigital regions during embryonic mouse limb development, in vivo and in vitro

      ANATOMY AND EMBRYOLOGY
    23. Perrotin, F; Haddad, G; Guichet, A; Paillet, C; Moraine, C; Body, G
      Prenatal ultrasonographic diagnosis of the popliteal pterygium syndrome

      PRENATAL DIAGNOSIS
    24. Lyu, KJ; Ko, TM
      Prenatal diagnosis of Apert syndrome with widely separated cranial sutures

      PRENATAL DIAGNOSIS
    25. Kantaputra, PN; Chalidapong, P
      Are triphalangeal thumb-polysyndactyly syndrome (TPTPS) and tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome(THPTTS) identical? A father with TPTPS and his daughter with THPTTS in a Thai family

      AMERICAN JOURNAL OF MEDICAL GENETICS
    26. Buttiker, V; Wojtulewicz, J; Wilson, M
      Imperforate anus in Feingold syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    27. MacLean, JE; Teshima, IE; Szatmari, P; Nowaczyk, MJM
      Ring chromosome 22 and autism: Report and review

      AMERICAN JOURNAL OF MEDICAL GENETICS
    28. Corona-Rivera, A; Corona-Rivera, JR; Bobadilla-Morales, L; Garcia-Cobian, TA; Corona-Rivera, E
      Holoprosencephaly, hypertelorism, and ectrodactyly in a boy with an apparently balanced de novo t(2;4)(q14.2;q35)

      AMERICAN JOURNAL OF MEDICAL GENETICS
    29. Franceschini, P; Licata, D; Di Cara, G; Guala, A; Franceschini, D; Genitori, L
      Macrocephaly-cutis marmorata telangiectatica congenita without cutis marmorata?

      AMERICAN JOURNAL OF MEDICAL GENETICS
    30. Yu, K; Herr, AB; Waksman, G; Ornitz, DM
      Loss of fibroblast growth factor receptor 2 ligand-binding specificity in Apert syndrome

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    31. Pilkington, S; Hearth, M; Richards, AM; Hobby, JAE
      Laurin-Sandrow syndrome - a surgical challenge

      BRITISH JOURNAL OF PLASTIC SURGERY
    32. Wong, FK; Gustafsson, B
      Popliteal pterygium syndrome in a Swedish family - clinical findings and genetic analysis with the van der Woude syndrome locus at lq32-q41

      ACTA ODONTOLOGICA SCANDINAVICA
    33. Ucakhan, OO; Atmaca, L; Sayli, BS; Sayar, C; Firat, E
      Bilateral abortive cryptophthalmos associated with oculocutaneous albinism

      ACTA OPHTHALMOLOGICA SCANDINAVICA
    34. Temple, IK; Browne, C; Hodgkins, P
      Anterior chamber eye anomalies, redundant skin and syndactyly - a new syndrome associated with breakpoints at 2q37.2 and 7q36.3

      CLINICAL DYSMORPHOLOGY
    35. Merino, R; Rodriguez-Leon, J; Macias, D; Ganan, Y; Economides, AN; Hurle, JM
      The BMP antagonist Gremlin regulates outgrowth, chondrogenesis and programmed cell death in the developing limb

      DEVELOPMENT
    36. Ekerot, L
      Correction of syndactyly: Advantages with a non-grafting technique and theuse of absorbable skin sutures

      SCANDINAVIAN JOURNAL OF PLASTIC AND RECONSTRUCTIVE SURGERY AND HAND SURGERY
    37. Ruggieri, M; Pavone, V; De Luca, D; Franzo, A; Tine, A; Pavone, L
      Congenital bone malformations in patients with neurofibromatosis type 1 (Nf1)

      JOURNAL OF PEDIATRIC ORTHOPAEDICS
    38. Balci, S; Altinok, G; Ozaltin, F; Aktas, D; Niron, EA; Onol, B
      Laryngeal atresia presenting as fetal ascites, olygohydramnios and lung appearance mimicking cystic adenomatoid malformation in a 25-week-old fetus with Fraser syndrome

      PRENATAL DIAGNOSIS
    39. Balci, S; Demirtas, M; Civelek, B; Piskin, M; Sensoz, O; Akarsu, AN
      Phenotypic variability of triphalangeal thumb-polysyndactyly syndrome linked to chromosome 7q36

      AMERICAN JOURNAL OF MEDICAL GENETICS
    40. Williams, MS; Williams, JL; Wargowski, DS; Pauli, RM; Pletcher, BA
      Filippi syndrome: Report of three additional cases

      AMERICAN JOURNAL OF MEDICAL GENETICS
    41. Paravatty, RP; Ahsan, A; Sebastian, BT; Pai, KM; Dayal, PK
      Apert syndrome: A case report with discussion of craniofacial features

      QUINTESSENCE INTERNATIONAL
    42. Fontenot, C; Ortenberg, J; Faust, D
      Hypospadiac or intact foreskin graft for syndactyly repair

      JOURNAL OF PEDIATRIC SURGERY
    43. Janssen, HCJP; Schaap, C; Vandevijver, N; Moerman, P; de Die-Smulders, CEM; Fryns, JP
      Two sibs with microcephaly, hygroma colli, renal dysplasia, and cutaneous syndactyly: a new lethal MCA syndrome?

      JOURNAL OF MEDICAL GENETICS
    44. Mempel, M; Abeck, D; Lange, I; Strom, K; Caliebe, A; Beham, A; Kautza, M; Worret, WI; Neubauer, BA; Ring, J; Schroder, H; Folster-Holst, R
      The wide spectrum of clinical expression in Adams-Oliver syndrome: a report of two cases

      BRITISH JOURNAL OF DERMATOLOGY
    45. THOMSEN M; SCHNEIDER U; WEBER M; NIETHARD FU
      THE DIFFERENT APPEARANCE OF THE OCULODENTODIGITAL DYSPLASIA SYNDROME

      Journal of pediatric orthopedics. Part B
    46. MCGAUGHRAN J; MOORE L; RUSSELL S; DONNAI D
      SYNDACTYLY, MICROGNATHIA AND SKELETAL ANOMALIES - A NEW SYNDROME

      Clinical dysmorphology
    47. Kaufman, MH; Chang, HH
      Influence of anaesthetic agent on limb abnormalities observed following amniotic sac puncture

      EUROPEAN JOURNAL OF MORPHOLOGY
    48. Kramer, RC; Hildreth, DH; Brinker, MR; Bennett, JB; Thompson, L; Lumsden, RM; Cain, TE
      A comparison of patients with different types of syndactyly

      JOURNAL OF PEDIATRIC ORTHOPAEDICS
    49. BRODIE SG; KITOH H; LIPSON M; SIFRYPLATT M; WILCOX WR
      THANATOPHORIC DYSPLASIA TYPE-I WITH SYNDACTYLY

      American journal of medical genetics
    50. ANDERSON AJ; STEPHAN MJ; WALKER WO; KELLEY RI
      VARIANT RSH SMITH-LEMLI-OPITZ-SYNDROME WITH ATYPICAL STEROL-METABOLISM/

      American journal of medical genetics
    51. NOWACZYK MJM; WHELAN DT; HILL RE
      SMITH-LEMLI-OPITZ-SYNDROME - PHENOTYPIC EXTREME WITH MINIMAL CLINICALFINDINGS

      American journal of medical genetics
    52. GRANGE DK; BALFOUR IC; CHEN SC; WOOD EG
      FAMILIAL SYNDROME OF PROGRESSIVE ARTERIAL OCCLUSIVE DISEASE CONSISTENT WITH FIBROMUSCULAR DYSPLASIA, HYPERTENSION, CONGENITAL CARDIAC DEFECTS, BONE FRAGILITY, BRACHYSYNDACTYLY, AND LEARNING-DISABILITIES

      American journal of medical genetics
    53. HWANG SJ; BEATY TH; MCINTOSH I; HEFFERON T; PANNY SR
      ASSOCIATION BETWEEN HOMEOBOX-CONTAINING GENE MSX1 AND THE OCCURRENCE OF LIMB DEFICIENCY

      American journal of medical genetics
    54. Castilla, EE; Lugarinho, R; Dutra, MD; Salgado, LJ
      Associated anomalies in individuals with polydactyly

      AMERICAN JOURNAL OF MEDICAL GENETICS
    55. PARK MS; HAHN SH; HONG CH; KIM JS; KIM HS
      EXTENSIVE FORM OF APLASIA-CUTIS-CONGENITA - A NEW SYNDROME

      Journal of Medical Genetics
    56. PERCIN EF; PERCIN S; EGILMEZ H; SEZGIN I; OZBAS F; AKARSU AN
      MESOAXIAL COMPLETE SYNDACTYLY AND SYNOSTOSIS WITH HYPOPLASTIC THUMBS - AN UNUSUAL COMBINATION OR HOMOZYGOUS EXPRESSION OF SYNDACTYLY TYPE-I

      Journal of Medical Genetics
    57. GOHO C
      DENTAL FINDINGS IN SAETHRE-CHOTZEN-SYNDROME (ACROCEPHALOSYNDACTYLY TYPE-III) - REPORT OF CASE

      Journal of dentistry for children
    58. CHANG HH; TSE Y; KAUFMAN MH
      ANALYSIS OF INTERDIGITAL SPACES DURING MOUSE LIMB DEVELOPMENT AT INTERVALS FOLLOWING AMNIOTIC SAC PUNCTURE

      Journal of Anatomy
    59. DESMET L; FABRY G
      KELOID FORMATION IN SYNDACTYLY RELEASE - REPORT OF 2 CASES

      Journal of pediatric orthopedics. Part B
    60. PREVEL CD; EPPLEY BL; MCCARTY M
      ACROCEPHALOSYNDACTYLY SYNDROMES - A REVIEW

      The Journal of craniofacial surgery
    61. KAUFMANN K; BALDINGER S; PRATT L
      ULTRASOUND DETECTION OF APERT-SYNDROME - A CASE-REPORT AND LITERATURE-REVIEW

      American journal of perinatology
    62. COURTENS W; LEVI S; VERBELEN F; VERLOES A; VAMOS E
      FEINGOLD-SYNDROME - REPORT OF A NEW FAMILY AND REVIEW

      American journal of medical genetics
    63. MENDOZA HR; VALIENTE MD
      A NEWLY RECOGNIZED AUTOSOMAL-DOMINANT ECTODERMAL DYSPLASIA SYNDROME -THE ODONTO-TRICHO-UNGUAL-DIGITAL-PALMAR-SYNDROME

      American journal of medical genetics
    64. INNIS JW; ASHER JH; POZNANSKI AK; SHELDON S
      AUTOSOMAL-DOMINANT MICROCEPHALY WITH NORMAL INTELLIGENCE, SHORT PALPEBRAL FISSURES, AND DIGITAL ANOMALIES

      American journal of medical genetics
    65. SHAPIRO RE; GRIFFIN JW; STINE OC
      EVIDENCE FOR GENETIC ANTICIPATION IN THE OCULODENTODIGITAL SYNDROME

      American journal of medical genetics
    66. ELCIOGLU N; ATASU M; CENANI A
      DERMATOGLYPHICS IN PATIENTS WITH CENANI-LENZ TYPE SYNDACTYLY - STUDIES IN A NEW CASE

      American journal of medical genetics
    67. FREIHOFER HPM; WALJI S; BRUNNER HG
      ECTODERMAL DYSPLASIA, CLEFT LIP PALATE, AND SEVERE CUTANEOUS AND OSSEOUS SYNDACTYLY IN A MENTALLY-RETARDED GIRL - A NEW MULTIPLE MALFORMATION SYNDROME/

      American journal of medical genetics
    68. NIXON J; OLDRIDGE M; WILKIE AOM; SMITH K
      INTERSTITIAL DELETION OF 2Q ASSOCIATED WITH CRANIOSYNOSTOSIS, OCULAR COLOBOMA, AND LIMB ABNORMALITIES - CYTOGENETIC AND MOLECULAR INVESTIGATION

      American journal of medical genetics
    69. VASIL M; BAXOVA A; KOZLOWSKI K
      SEVERE LIMB ABNORMALITIES - NIEVERGELT OR NEW SYNDROME

      American journal of medical genetics
    70. SORGE G; PAVONE L; POLIZZI A; MAUCERI L; LEONARDI RM; TRIPI T; OPITZ JM
      ANOTHER NEW FORM, THE PALAGONIA TYPE OF ACROFACIAL DYSOSTOSIS IN A SICILIAN FAMILY

      American journal of medical genetics
    71. KAWAME H; PAGON RA; HUDGINS L
      DIGITAL ANOMALIES, MICROCEPHALY, AND NORMAL INTELLIGENCE - NEW SYNDROME OR FEINGOLD SYNDROME

      American journal of medical genetics
    72. KOZLOWSKI K; KRAJEWSKA M
      MENTAL-RETARDATION, POSTAXIAL POLYDACTYLY, PHALANGEAL HYPOPLASIA, 2-3TOE SYNDACTYLY, UNUSUAL FACE, UNCOMBABLE HAIR - NEW SYNDROME

      American journal of medical genetics
    73. OATES SD; GOSAIN AK
      SYNDACTYLY REPAIR PERFORMED SIMULTANEOUSLY WITH CIRCUMCISION - USE OFFORESKIN AS A SKIN-GRAFT DONOR SITE

      Journal of pediatric surgery
    74. LIN KJ; WANG WN
      MOEBIUS SYNDROME - REPORT OF CASE

      Journal of dentistry for children
    75. WILLIAMS PG; HERSH JH; YEN FF; BARCH MJ; KLEINERT HE; KUNZ J; KALFFSUSKE M
      GREIG CEPHALOPOLYSYNDACTYLY SYNDROME - ALTERED PHENOTYPE OF A MICRODELETION SYNDROME DUE TO THE PRESENCE OF A CYTOGENETIC ABNORMALITY

      Clinical genetics
    76. ORRICO A; HAYEK G
      AN ADDITIONAL CASE OF CRANIODIGITAL SYNDROME - VARIABLE EXPRESSION OFTHE FILIPPI-SYNDROME

      Clinical genetics
    77. TERHAAR O; MICKE O; REIMER P; PETERS PE
      RADIOLOGICAL AND CLINICAL ASPECTS OF POLA ND SYNDROME

      RoFo. Fortschritte auf dem Gebiete der Rontgenstrahlen und der neuenbildgebenden Verfahren
    78. ISIK S; SELMANPAKOGLU N; ACIKEL C
      THE USE OF TISSUE EXPANDERS IN SYNDACTYLY REPAIR

      European journal of plastic surgery
    79. AMR SS
      UNILATERAL CRYPTOPHTHALMOS WITH RENAL AGENESIS AND SYNDACTYLY (FRASER-SYNDROME) - REPORT OF A CASE WITH REVIEW OF THE LITERATURE

      Saudi medical journal
    80. SENO H; YANAI A; SUGINO H; INOUE M; TAKEI T; MIYAKE I
      ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT-LIP SYNDROME - CASE-REPORT

      Scandinavian journal of plastic and reconstructive surgery and hand surgery
    81. ROBIN NH; SEGEL B; CARPENTER G; MUENKE M
      CRANIOSYNOSTOSIS, PHILADELPHIA TYPE - A NEW AUTOSOMAL-DOMINANT SYNDROME WITH SAGITTAL CRANIOSYNOSTOSIS AND SYNDACTYLY OF THE FINGERS AND TOES

      American journal of medical genetics
    82. GREEN AJ; SANDFORD RN; DAVISON BCC
      AN AUTOSOMAL-DOMINANT SYNDROME OF RENAL AND ANOGENITAL MALFORMATIONS WITH SYNDACTYLY

      Journal of Medical Genetics
    83. ZENTENO JC; AGUINAGA M; CHAVEZ V; SASTRE N; RIVERA MR; KOFMANALFARO S
      TRIPHALANGEAL THUMB AND BRACHYECTRODACTYLY SYNDROME - AN UNCOMMON ENTITY WITH EVIDENCE OF GEOGRAPHIC-DISTRIBUTION

      Clinical genetics
    84. HENNEKAM RCM; COHEN MM
      HYPOTHESIS - PATIENT WITH POSSIBLE DISTURBANCE IN PROGRAMMED CELL-DEATH

      European journal of human genetics
    85. SYKES AM; GRAY RR
      ANSWER TO CASE-OF-THE-MONTH NUMBER-33 - HOLT-GRAM SYNDROME

      Canadian Association of Radiologists journal
    86. KARAS DE; RESPLER DS
      FRASER SYNDROME - A CASE-REPORT AND REVIEW OF THE OTOLARYNGOLOGIC MANIFESTATIONS

      International journal of pediatric otorhinolaryngology
    87. ILYINA HG; AMOASHY DS; GRYGORY HA
      NEW ECTODERMAL DYSPLASIA WITH MENTAL-RETARDATION AND SYNDACTYLY

      American journal of medical genetics
    88. SAYLI BS; AKARSU AN; ALTAN S
      ANOPHTHALMOS-SYNDACTYLY (WAARDENBURG) SYNDROME WITHOUT OLIGODACTYLY OF TOES

      American journal of medical genetics
    89. NORTON KK; CAREY JC; GUTMANN DH
      OCULODENTODIGITAL DYSPLASIA WITH CEREBRAL WHITE-MATTER ABNORMALITIES IN A 2-GENERATION FAMILY

      American journal of medical genetics
    90. CAMERA G; CAMERA A; POZZOLO S; COSTA M; MANTERO R
      F-SYNDROME (F-FORM OF ACRO-PECTORO-VERTEBRAL DYSPLASIA) - REPORT ON A2ND FAMILY

      American journal of medical genetics
    91. COHEN MM; KREIBORG S
      HANDS AND FEET IN THE APERT SYNDROME

      American journal of medical genetics
    92. TORIELLO HV; HIGGINS JV
      CRANIODIGITAL SYNDROMES - REPORT OF A CHILD WITH FILIPPI SYNDROME ANDDISCUSSION OF DIFFERENTIAL-DIAGNOSIS

      American journal of medical genetics
    93. MARTINEZFRIAS ML; MARTIN M; PARDO M; DELASHERAS FF; FRIAS JL
      DISTAL APHALANGIA, SYNDACTYLY, AND EXTRA METATARSAL, ASSOCIATED WITH SHORT STATURE, MICROCEPHALY, AND BORDERLINE INTELLIGENCE - A NEW AUTOSOMAL-DOMINANT DISORDER

      American journal of medical genetics
    94. CAMERA G; CAMERA A; POZZOLO S; COSTA M; MANTERO R
      SYNPOLYDACTYLY (TYPE-II SYNDACTYLY) WITH APLASIA HYPOPLASIA OF THE MIDDLE PHALANGES OF THE TOES - REPORT ON A FAMILY WITH 8 AFFECTED MEMBERS IN 4 GENERATIONS

      American journal of medical genetics
    95. OZGUNEN T; EVRUKE C; KADAYIFCI O; DEMIR C; ARIDOGAN N; VARDAR MA
      FRASER SYNDROME

      International journal of gynaecology and obstetrics
    96. GARRAGHTY PE; MUJA N
      POSSIBLE USE-DEPENDENT CHANGES IN ADULT PRIMATE SOMATOSENSORY CORTEX

      Brain research
    97. CANTRELL SB; MOORE MH; TROTT JA; MORRIS RJ; DAVID DJ
      PHENOTYPIC VARIATION IN ACROCEPHALOSYNDACTYLY SYNDROMES - UNUSUAL FINDINGS IN PATIENT WITH FEATURES OF APERT AND SAETHRE-CHOTZEN SYNDROMES

      The Cleft palate-craniofacial journal
    98. SEKHON LHS; MORGAN MK; JOHNSTON IH
      SYNDACTYLY AND INTRACRANIAL ARTERIOVENOUS MALFORMATION - CASE-REPORT

      British journal of neurosurgery
    99. COULON P; LAN PTC; ADENIS JP; VERIN P
      BILATERAL COMPLETE CRYPTOPHTHALMOS - CASE -REPORT AND LITERATURE-REVIEW

      Journal francais d'ophtalmologie
    100. RODRIGUEZ JI; JIMENEZHEFFERNAN JA; LEAL J
      SCHINZEL-GIEDION SYNDROME - AUTOPSY REPORT AND ADDITIONAL CLINICAL MANIFESTATIONS

      American journal of medical genetics


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Documento generato il 26/10/20 alle ore 06:15:10