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Volumn 158 A, Issue 7, 2012, Pages 1793-1797

Periventricular heterotopia with white matter abnormalities associated with 6p25 deletion

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; BRAIN MALFORMATION; BRAIN VENTRICLE DILATATION; CASE REPORT; CEREBELLUM HYPOPLASIA; CHILD; CHROMOSOME DELETION; CHROMOSOME DELETION 6P; CHROMOSOME SEGREGATION; CHROMOSOME TRANSLOCATION; CLINICAL EXAMINATION; COMPARATIVE GENOMIC HYBRIDIZATION; CONVERGENT STRABISMUS; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; DIVERGENT STRABISMUS; FACE DYSMORPHIA; FEMALE; GENETIC ASSOCIATION; HAND MALFORMATION; HAND RADIOGRAPHY; HUMAN; HYPERMETROPIA; JOINT LAXITY; LETTER; MALE; MICROARRAY ANALYSIS; MILD COGNITIVE IMPAIRMENT; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE IMAGING; PERIVENTRICULAR HETEROTOPIA; PHENOTYPE; PRIORITY JOURNAL; SCHOOL CHILD; WHITE MATTER;

EID: 84862689345     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.35416     Document Type: Letter
Times cited : (27)

References (12)
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    • DeScipio, C.1
  • 6
    • 80755175446 scopus 로고    scopus 로고
    • Dysmyelination of the cerebral white matter with microdeletion at 6p25
    • Kapoor S, Mukherjee SB, Shroff D, Arora R. 2011. Dysmyelination of the cerebral white matter with microdeletion at 6p25. Indian Pediatr 48: 727- 729.
    • (2011) Indian Pediatr , vol.48 , pp. 727-729
    • Kapoor, S.1    Mukherjee, S.B.2    Shroff, D.3    Arora, R.4
  • 8
    • 0037092595 scopus 로고    scopus 로고
    • Molecular genetics of Axenfeld-Rieger malformations
    • Lines MA, Kozlowski K, Walter MA. 2002. Molecular genetics of Axenfeld-Rieger malformations. Hum Mol Genet 11: 1177- 1184.
    • (2002) Hum Mol Genet , vol.11 , pp. 1177-1184
    • Lines, M.A.1    Kozlowski, K.2    Walter, M.A.3
  • 11
    • 0022889651 scopus 로고
    • Dandy-Walker (like) malformation, atrio-ventricular septal defect and a similar pattern of minor anomalies in 2 sisters: A new syndrome?
    • Ritscher D, Schinzel A, Boltshauser E, Briner J, Arbenz U, Sigg P. 1987. Dandy-Walker (like) malformation, atrio-ventricular septal defect and a similar pattern of minor anomalies in 2 sisters: A new syndrome? Am J Med Genet 26: 481- 491.
    • (1987) Am J Med Genet , vol.26 , pp. 481-491
    • Ritscher, D.1    Schinzel, A.2    Boltshauser, E.3    Briner, J.4    Arbenz, U.5    Sigg, P.6
  • 12
    • 35348924902 scopus 로고    scopus 로고
    • Cortical dysplasia and skull defects in mice with a Foxc1 allele reveal the role of meningeal differentiation in regulating cortical development
    • Zarbalis K, Siegenthaler JA, Choe Y, May SR, Peterson AS, Pleasure SJ. 2007. Cortical dysplasia and skull defects in mice with a Foxc1 allele reveal the role of meningeal differentiation in regulating cortical development. Proc Natl Acad Sci USA 104: 14002- 14007.
    • (2007) Proc Natl Acad Sci USA , vol.104 , pp. 14002-14007
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.