FRONTONASAL MALFORMATION AND THE OCULOAURICULOVERTEBRAL SPECTRUM - THE OCULOAURICULOFRONTONASAL SYNDROME

被引:0
|
作者
BRADDOCK, SR
CAREY, JC
MORALES, L
HASKINS, RC
机构
[1] UNIV UTAH,DEPT PEDIAT,SALT LAKE CITY,UT 84112
[2] PRIMARY CHILDRENS MED CTR,SALT LAKE CITY,UT 84103
来源
CLINICAL RESEARCH | 1991年 / 39卷 / 01期
关键词
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
引用
收藏
页码:A8 / A8
页数:1
相关论文
共 50 条
  • [1] Frontonasal malformation and the oculoauriculovertebral spectrum: The oculoauriculofrontonasal syndrome
    Casey, HD
    Braddock, SR
    Haskins, RC
    Carey, JC
    Morales, L
    CLEFT PALATE-CRANIOFACIAL JOURNAL, 1996, 33 (06): : 519 - 523
  • [2] PATTERN OF CARDIAC MALFORMATION IN OCULOAURICULOVERTEBRAL SPECTRUM
    KUMAR, A
    FRIEDMAN, JM
    TAYLOR, GP
    PATTERSON, MWH
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 46 (04): : 423 - 426
  • [3] Oculoauriculovertebral spectrum with radial defects: a new syndrome or an extension of the oculoauriculovertebral spectrum? Report of fourteen Brazilian cases and review of the literature
    Vendramini, Siulan
    Richieri-Costa, Antonio
    Guion-Almeida, Maria Leine
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2007, 15 (04) : 411 - 421
  • [4] Oculoauriculovertebral spectrum with radial defects: a new syndrome or an extension of the oculoauriculovertebral spectrum? Report of fourteen Brazilian cases and review of the literature
    Siulan Vendramini
    Antonio Richieri-Costa
    Maria Leine Guion-Almeida
    European Journal of Human Genetics, 2007, 15 : 411 - 421
  • [5] Frontonasal dysplasia; phenotypic spectrum of related malformation syndromes and their molecular basis
    Kayserili, Hulya
    CURRENT OPINION IN BIOTECHNOLOGY, 2011, 22 : S24 - S25
  • [6] FRONTONASAL DYSPLASIA IN THE KLIPPEL-FEIL SYNDROME - A NEW ASSOCIATED MALFORMATION
    FRAGOSO, R
    CIDGARCIA, A
    HERNANDEZ, A
    NAZARA, Z
    CANTU, JM
    CLINICAL GENETICS, 1982, 22 (05) : 270 - 273
  • [7] A dominantly inherited syndrome with frontonasal malformation : variant of Teebi hypertelorism syndrome or new entity
    Verloes, A
    Baumann, C
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 267 - 267
  • [8] Characterizing the oculoauriculofrontonasal syndrome
    Gabbett, Michael T.
    Robertson, Stephen R.
    Broadbent, Roland
    Aftimos, Salim
    Sachdev, Rani
    Nezarati, Marjan M.
    CLINICAL DYSMORPHOLOGY, 2008, 17 (02) : 79 - 85
  • [9] OCULOAURICULOVERTEBRAL SPECTRUM AND CEREBRAL ANOMALIES
    SCHRANDERSTUMPEL, CTRM
    DEDIESMULDERS, CEM
    HENNEKAM, RCM
    FRYNS, JP
    BOUCKAERT, PXJM
    BROUWER, OF
    DACOSTA, JJ
    LOMMEN, EJP
    MAASWINKELMOOY, PD
    JOURNAL OF MEDICAL GENETICS, 1992, 29 (05) : 326 - 331
  • [10] Two Siblings with Kaufman Oculocerebrofacial Syndrome Resembling Oculoauriculovertebral Spectrum
    Urel-Demir, Gizem
    Aydin, Busra
    Karaosmanoglu, Beren
    Akgun-Dogan, Ozlem
    Taskiran, Ekim Zihni
    Simsek-Kiper, Pelin Ozlem
    Utine, Gulen Eda
    Boduroglu, Koray
    MOLECULAR SYNDROMOLOGY, 2021, 12 (02) : 106 - 111