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Volumn 58, Issue 1, 1996, Pages 7-16

Absence makes the search grow longer

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL MODEL; CORPUS CALLOSUM AGENESIS; CYTOGENETICS; EDITORIAL; EMBRYOLOGY; GENE MAPPING; GENETIC HETEROGENEITY; HUMAN; MALFORMATION SYNDROME; NONHUMAN; PERIPHERAL NEUROPATHY; PRIORITY JOURNAL;

EID: 0029655911     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Editorial
Times cited : (93)

References (8)
  • 2
    • 0345802046 scopus 로고
    • The Andermann syndrome: Agenesis of the corpus callosum and sensorimotor neuropathy
    • Lassonde M, Jeeves MA (eds) Plenum, New York
    • Andermann F, Andermann E (1994) The Andermann syndrome: agenesis of the corpus callosum and sensorimotor neuropathy. In: Lassonde M, Jeeves MA (eds) Callosal agenesis: a natural split brain? Plenum, New York, pp 19-26
    • (1994) Callosal Agenesis: A Natural Split Brain? , pp. 19-26
    • Andermann, F.1    Andermann, E.2
  • 4
    • 0020532005 scopus 로고
    • De novo interstitial deletion of the long arm of chromosome 2 in a malformed newborn with a karyotype: 46.XY,del(2)(q12q14)
    • Antich J, Carbonell X, Mas J, Clusellas N (1983) De novo interstitial deletion of the long arm of chromosome 2 in a malformed newborn with a karyotype: 46.XY,del(2)(q12q14). Acta Paediatr Scand 72:631-633
    • (1983) Acta Paediatr Scand , vol.72 , pp. 631-633
    • Antich, J.1    Carbonell, X.2    Mas, J.3    Clusellas, N.4
  • 5
    • 0016039574 scopus 로고
    • Agénésie partielle du corps calleux, avec anomalies ocularies multiples et aberration chromosomique exceptionelle
    • Ardouin M, Urvoy M, LeMare B, Lessard M, Senecal J (1974) Agénésie partielle du corps calleux, avec anomalies ocularies multiples et aberration chromosomique exceptionelle. Rev Otoneuroophtalmol 46:143-147
    • (1974) Rev Otoneuroophtalmol , vol.46 , pp. 143-147
    • Ardouin, M.1    Urvoy, M.2    Lemare, B.3    Lessard, M.4    Senecal, J.5
  • 6
    • 0023806505 scopus 로고
    • Clinical features in a de novo interstitial deletion 15q13 to q15
    • Autio S, Pihko H, Tengström C (1988) Clinical features in a de novo interstitial deletion 15q13 to q15. Clin Genet 34:293-298
    • (1988) Clin Genet , vol.34 , pp. 293-298
    • Autio, S.1    Pihko, H.2    Tengström, C.3
  • 7
    • 0023684795 scopus 로고
    • Abnormalities of corpus callosum in patients with inherited metabolic diseases
    • Bamforth F, Bamforth S, Poskitt K, Applegarth D, Hall J (1988) Abnormalities of corpus callosum in patients with inherited metabolic diseases. Lancet 2:451
    • (1988) Lancet , vol.2 , pp. 451
    • Bamforth, F.1    Bamforth, S.2    Poskitt, K.3    Applegarth, D.4    Hall, J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.