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Volumn 28, Issue 6, 1997, Pages 335-337

Abnormal myelination in a patient with ring chromosome 18

Author keywords

Abnormal myelination; Microsatellite marker; Myelin basic protein; Ring chromosome 18

Indexed keywords

MICROSATELLITE DNA; MYELIN BASIC PROTEIN;

EID: 0030823071     PISSN: 0174304X     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-973727     Document Type: Article
Times cited : (15)

References (10)
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  • 3
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    • Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion
    • Knoll, J. H. M., R. D. Nicholls, R. E. Magenis, J. M. Jr. Graham, M. Lande, S. A. Latt: Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion. Am. J. Med. Genet. 32 (1989) 285-290
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    • Knoll, J.H.M.1    Nicholls, R.D.2    Magenis, R.E.3    Graham Jr., J.M.4    Lande, M.5    Latt, S.A.6
  • 4
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    • Defective biosynthesis of proteolipid protein in Pelizaeus-Merzbacher disease
    • Koeppen, A. H., N. A. Ronca, E. A. Greenfield, M. B. Haus: Defective biosynthesis of proteolipid protein in Pelizaeus-Merzbacher disease. Ann. Neurol. 21 (1986) 159-170
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  • 6
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    • Tetranucleotide repeat polymorphism at the human myelin basic protein gene (MBP)
    • Polymeropoulos, M. H., H. Xiao, C. R. Merril: Tetranucleotide repeat polymorphism at the human myelin basic protein gene (MBP). Hum. Mol. Genet. 1 (1992) 658
    • (1992) Hum. Mol. Genet. , vol.1 , pp. 658
    • Polymeropoulos, M.H.1    Xiao, H.2    Merril, C.R.3
  • 7
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    • Characterization of cloned cDNA representing rat myelin basic protein: Absence of expression in brain of shiverer mutant mice
    • Roach, A., K. Boylan, S. Horvath: Characterization of cloned cDNA representing rat myelin basic protein: absence of expression in brain of shiverer mutant mice. Cell 34 (1983) 799-806
    • (1983) Cell , vol.34 , pp. 799-806
    • Roach, A.1    Boylan, K.2    Horvath, S.3
  • 8
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    • Localization of the human myelin basic protein gene (MBP) to region 18q22-qter by in situ hybridization
    • Saxe, D. F., N. Takahashi, L. Hood, M. I. Simon: Localization of the human myelin basic protein gene (MBP) to region 18q22-qter by in situ hybridization. Cytogenet. Cell Genet. 39 (1985) 246-249
    • (1985) Cytogenet. Cell Genet. , vol.39 , pp. 246-249
    • Saxe, D.F.1    Takahashi, N.2    Hood, L.3    Simon, M.I.4
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    • The reflection of histology in MR imaging of Pelizaeus-Merzbacher disease
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    • Segmental spinal muscular atrophy and dermatological findings in a patient with chromosome 18q deletion
    • Weiss, B. J., J. Kamholz, A. Ritter, E. H. Zackai, D. M. McDonald-McGinn, B. Emmanuel et al: Segmental spinal muscular atrophy and dermatological findings in a patient with chromosome 18q deletion. Ann. Neurol. 30 (1991) 419-423
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.