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Volumn 140 A, Issue 8, 2006, Pages 900-902

HOXA1 mutations are not a common cause of Duane anomaly [3]

Author keywords

[No Author keywords available]

Indexed keywords

DUANE RETRACTION SYNDROME; GAZE; GENE; GENE ISOLATION; GENE MUTATION; GENETIC ANALYSIS; GENETIC SCREENING; GENETIC TRAIT; HOXA1 GENE; HUMAN; LETTER; PRIORITY JOURNAL; STRABISMUS;

EID: 33645560350     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.31167     Document Type: Letter
Times cited : (23)

References (17)
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    • Cross, H.E.1    Pfaffenbach, D.D.2
  • 4
    • 0033987736 scopus 로고    scopus 로고
    • Mutation nomenclature extensions and suggestions to describe complex mutations: A discussion
    • den Dunnen JT, Antonarakis SE. 2000. Mutation nomenclature extensions and suggestions to describe complex mutations: A discussion. Hum Mutat 15:7-12.
    • (2000) Hum Mutat , vol.15 , pp. 7-12
    • Den Dunnen, J.T.1    Antonarakis, S.E.2
  • 5
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    • Applications of molecular genetics to the understanding of congenital ocular motility disorders
    • Engle EC. 2002. Applications of molecular genetics to the understanding of congenital ocular motility disorders. Ann NY Acad Sci 956:55-63.
    • (2002) Ann NY Acad Sci , vol.956 , pp. 55-63
    • Engle, E.C.1
  • 6
    • 0033943555 scopus 로고    scopus 로고
    • Confirmation of linkage of Duane's syndrome and refinement of the disease locus to an 8.8-cM interval on chromosome 2q31
    • Evans JC, Frayling TM, Ellard S, Gutowski NJ. 2000. Confirmation of linkage of Duane's syndrome and refinement of the disease locus to an 8.8-cM interval on chromosome 2q31. Hum Genet 106:636-638.
    • (2000) Hum Genet , vol.106 , pp. 636-638
    • Evans, J.C.1    Frayling, T.M.2    Ellard, S.3    Gutowski, N.J.4
  • 8
    • 0018893694 scopus 로고
    • Bilateral Duane's retraction syndrome: A clinical-pathological case report
    • Hotchkiss MG, Miller NR, Clark AW, Green WG. 1980. Bilateral Duane's retraction syndrome: A clinical-pathological case report. Arch Ophthalmol 98:870-874.
    • (1980) Arch Ophthalmol , vol.98 , pp. 870-874
    • Hotchkiss, M.G.1    Miller, N.R.2    Clark, A.W.3    Green, W.G.4
  • 9
    • 0033667613 scopus 로고    scopus 로고
    • Discovery of allelic variants of HOXA1 and HOXB1: Genetic susceptibility to autism spectrum disorders
    • Ingram JL, Stodgell CJ, Hyman SL, Figlewicz DA, Weitkamp LR, Rodier PM. 2000. Discovery of allelic variants of HOXA1 and HOXB1: Genetic susceptibility to autism spectrum disorders. Teratology 62:393-405.
    • (2000) Teratology , vol.62 , pp. 393-405
    • Ingram, J.L.1    Stodgell, C.J.2    Hyman, S.L.3    Figlewicz, D.A.4    Weitkamp, L.R.5    Rodier, P.M.6
  • 11
    • 0014791574 scopus 로고
    • Inheritance of Duane's syndrome
    • Kirkham T. 1970. Inheritance of Duane's syndrome. Br J Ophthalmol 54:323-329.
    • (1970) Br J Ophthalmol , vol.54 , pp. 323-329
    • Kirkham, T.1
  • 15
    • 0015459795 scopus 로고
    • Congenital anomalies in Duane's retraction syndrome
    • Pfaffenbach D, Cross H, Kearns T. 1972. Congenital anomalies in Duane's retraction syndrome. Arch Ophthalmol 88:635.
    • (1972) Arch Ophthalmol , vol.88 , pp. 635
    • Pfaffenbach, D.1    Cross, H.2    Kearns, T.3
  • 17
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    • Mobius syndrome redefined: A syndrome of rhombencephalic maldevelopment
    • Verzijl HT, van der Zwaag B, Cruysberg JR, Padberg GW. 2003. Mobius syndrome redefined: A syndrome of rhombencephalic maldevelopment. Neurology 61:327-333.
    • (2003) Neurology , vol.61 , pp. 327-333
    • Verzijl, H.T.1    Van Der Zwaag, B.2    Cruysberg, J.R.3    Padberg, G.W.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.