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au.\*:("GOUW WL")

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COMPLETE DEFICIENCY OF CONSTITUTIVE HETEROCHROMATIN ON A HUMAN CHROMOSOME 9BUYS CHCM; YPMA JMM; GOUW WL et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 49; NO 2; PP. 129-132; BIBL. 8 REF.Article

RAPID IDENTIFICATION OF CHROMOSOMES CARRYING SILVER-STAINED NUCLEOLUS-ORGANIZING REGIONS: APPLICATION TO A CASE OF 21/21 ROBERTSONIAN TRANSLOCATIONBUYS CHCM; OSINGA J; GOUW WL et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 44; NO 2; PP. 173-180; BIBL. 2 P.Article

PATERNAL TRANSMISSION OF A B/D TRANSLOCATION, T (4P-; 14P+ OR 15P+), RESULTING IN A PARTIAL 4P TRISOMY = TRANSMISSION PATERNELLE D'UNE TRANSLOCATION B/D, T (4P-; 14P+ OU 15P+), AVEC POUR RESULTAT UNE TRISOMIE PARTIELLE 4P)GOUW WL; ANDERS GJPA; TEN KATE LP et al.sdHUMANGENETIK; DTSCH.; DA. 197; VOL. 16; NO 3; PP. 251-259; BIBL. 10 REF.Serial Issue

HETEROGENEITY OF HUMAN CHROMOSOME 9 CONSTITUTIVE HETEROCHROMATIN AS REVEALED BY SEQUENTIAL DISTAMYCIN A/DAPI STAINING AND C-BANDINGBUYS CHCM; GOUW WL; BLENKERS JAM et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 1; PP. 28-30; BIBL. 24 REF.Article

SHOULD WE SCREEN ALL NEWBORNS FOR CYSTIC FIBROSIS.TEN KATE LP; FEENSTRA DE GOOYER I; PLOEG DE GROOT G et al.1978; INTERNATION. J. EPIDEMIOL.; GBR; DA. 1978; VOL. 7; NO 4; PP. 323-330; BIBL. 20 REF.Article

A COMPARISON OF CONSTITUTIVE HETEROCHROMATIN STAINING METHODS IN TWO CASES OF FAMILIAL HETEROCHROMATIN DEFICIENCIESBUYS CHCM; ANDERS GJPA; GOUW WL et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 52; NO 1; PP. 133-138; BIBL. 23 REF.Article

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