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Disruption of the mouse L1 gene leads to malformations of the nervous systemDAHME, M; BARTSCH, U; MARTINI, R et al.Nature genetics. 1997, Vol 17, Num 3, pp 346-349, issn 1061-4036Article

L1-associated diseases : clinical geneticists divide, molecular geneticists uniteFRANSEN, E; VAN CAMP, G; VITS, L et al.Human molecular genetics (Print). 1997, Vol 6, Num 10, pp 1625-1632, issn 0964-6906Article

L1 knockout mice show dilated ventricles, vermis hypoplasia and impaired exploration patternsFRANSEN, E; D'HOOGE, R; DE ZEEUW, C. I et al.Human molecular genetics (Print). 1998, Vol 7, Num 6, pp 999-1009, issn 0964-6906Article

A novel L1CAM mutation in a fetus detected by prenatal diagnosisPICCIONE, Maria; MATINA, Federico; FICHERA, Marco et al.European journal of pediatrics. 2010, Vol 169, Num 4, pp 415-419, issn 0340-6199, 5 p.Article

Crash syndrome : Mutations in L1CAM correlate with severity of the diseaseYAMASAKI, M; THOMPSON, P; LEMMON, V et al.Neuropediatrics. 1997, Vol 28, Num 3, pp 175-178, issn 0174-304XArticle

X-chromosomal gebundener Hydrozephalus (HSAS): Eine Erkrankung aus der Gruppe der CRASH-Syndrome = X-linked hydrocephalus (HSAS). One of the diseases of the group of CRASH-syndromesBRECHT, I; RESSLER, B; BODE, H et al.Monatsschrift für Kinderheilkunde. 2003, Vol 151, Num 12, pp 1311-1315, issn 0026-9298, 5 p.Article

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