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Volumn 103, Issue 3, 2002, Pages 305-306

Rhombencephalosynapsis

Author keywords

[No Author keywords available]

Indexed keywords

HOMEODOMAIN PROTEIN; TRANSCRIPTION FACTOR;

EID: 0036938203     PISSN: 00016322     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00401-001-0506-4     Document Type: Editorial
Times cited : (10)

References (18)
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    • Aydingoz, U.1    Cila, A.2    Aktan, G.3
  • 2
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    • Neuronal migration defects in the Dreher (Lmx1a) mutant mouse: Role of disorders of the glial limiting membrane
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    • Costa, C.1    Harding, B.2    Copp, A.J.3
  • 3
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    • Defects of blastogenesis: Counseling dilemmas in two families
    • De Jong G, Kirby PA (2000) Defects of blastogenesis: counseling dilemmas in two families. Am J Med Genet 91:175-179
    • (2000) Am. J. Med. Genet. , vol.91 , pp. 175-179
    • De Jong, G.1    Kirby, P.A.2
  • 4
    • 0000633090 scopus 로고
    • Die Rhombencephalosynapsis, eine systemisierte, Kleinhirnfehlbildung
    • Gross H (1959) Die Rhombencephalosynapsis, eine systemisierte, Kleinhirnfehlbildung. Arch Psych Neurol 199:537-552
    • (1959) Arch. Psych. Neurol. , vol.199 , pp. 537-552
    • Gross, H.1
  • 5
    • 0034213442 scopus 로고    scopus 로고
    • Dorsal patterning defects in the hindbrain, roof plate and skeleton in the dreher [dr(J)] mouse mutant
    • Manzanares M, Trainor PA, Ariza-McNaughton L, Nonchev S, Krumlauf R (2000) Dorsal patterning defects in the hindbrain, roof plate and skeleton in the dreher [dr(J)] mouse mutant. Mech Dev 94:147-156
    • (2000) Mech. Dev. , vol.94 , pp. 147-156
    • Manzanares, M.1    Trainor, P.A.2    Ariza-McNaughton, L.3    Nonchev, S.4    Krumlauf, R.5
  • 6
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    • The mouse Dreher gene Lmx1a controls formation of the roof plate in the vertebrate CNS
    • Millonig JH, Millen KJ, Hatten ME (2000) The mouse Dreher gene Lmx1a controls formation of the roof plate in the vertebrate CNS. Nature 403:764-769
    • (2000) Nature , vol.403 , pp. 764-769
    • Millonig, J.H.1    Millen, K.J.2    Hatten, M.E.3
  • 8
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    • Ein Kleinhirn ohne Wurm
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  • 9
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    • A new patient with rhombencephalosynapsis
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  • 10
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    • Rhombencephalosynapsis with facial anomalies and probable autosomal recessive inheritance: A case report
    • Romanengo M, Tortori-Donati P, Di Rocco M (1997) Rhombencephalosynapsis with facial anomalies and probable autosomal recessive inheritance: a case report. Clin Genet 52:184-186
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    • Romanengo, M.1    Tortori-Donati, P.2    Di Rocco, M.3
  • 11
    • 0026318511 scopus 로고
    • Isolated rhombencephalosynapsis diagnosed by magnetic resonance imaging
    • Savolaine ER, Fadell RJ, Patel YP (1991) Isolated rhombencephalosynapsis diagnosed by magnetic resonance imaging. Clin Imaging 15:125-129
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  • 13
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    • Sener RN (2000) Unusual MRI findings in rhombencephalosynapsis. Comput Med Imaging Graph 24:277-282
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  • 14
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    • Sergi, C.1    Hentze, S.2    Sohn, C.3    Voigtlander, T.4    Jung, C.5    Schmitt, H.P.6
  • 16
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    • Partial midline fusion of the cerebellar hemispheres with vertical folia: A new cerebellar malformation?
    • Takanashi J, Sugita K, Barkovich AJ, Takano H, Kohno Y (2000) Partial midline fusion of the cerebellar hemispheres with vertical folia: a new cerebellar malformation? Am J Neuroradiol 20:1151-1153
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    • Rhombencephalosynapsis with massive hydrocephalus: Case report and pathogenetic considerations
    • (this issue)
    • Yachnis AT (2002) Rhombencephalosynapsis with massive hydrocephalus: case report and pathogenetic considerations. Acta Neuropathol (this issue)
    • (2002) Acta Neuropathol.
    • Yachnis, A.T.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.