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Results: 1-9 |
Results: 9
ASSIGNMENT OF H7365 (C9ORF2) TO HUMAN-CHROMOSOME BAND 9Q31 BY SOMATIC-CELL HYBRID ANALYSIS AND FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: EIB DW MERKX GFM MARTENS GJM CREMERS FPM
Citation: Dw. Eib et al., ASSIGNMENT OF H7365 (C9ORF2) TO HUMAN-CHROMOSOME BAND 9Q31 BY SOMATIC-CELL HYBRID ANALYSIS AND FLUORESCENCE IN-SITU HYBRIDIZATION, Cytogenetics and cell genetics, 81(3-4), 1998, pp. 180-181
ASSIGNMENT OF THE CANALICULAR MULTIORGANIC ANION TRANSPORTER (CMOAT) GENE TO HUMAN-CHROMOSOME 10Q24 AND MOUSE CHROMOSOME 19D2
Authors: VANKUIJCK MA MERKX GFM KOOL M VANKESSEL AG BINDELS RJM DEEN PMT VANOS CH
Citation: Ma. Vankuijck et al., ASSIGNMENT OF THE CANALICULAR MULTIORGANIC ANION TRANSPORTER (CMOAT) GENE TO HUMAN-CHROMOSOME 10Q24 AND MOUSE CHROMOSOME 19D2, The FASEB journal, 11(3), 1997, pp. 149-149
ASSIGNMENT OF THE HUMAN ADIPOCYTE FATTY-ACID-BINDING PROTEIN GENE (FABP4) TO CHROMOSOME 8Q21 USING SOMATIC-CELL HYBRID AND FLUORESCENCE IN-SITU HYBRIDIZATION TECHNIQUES
Authors: PRINSEN CFM DEBRUIJN DRH MERKX GFM VEERKAMP JH
Citation: Cfm. Prinsen et al., ASSIGNMENT OF THE HUMAN ADIPOCYTE FATTY-ACID-BINDING PROTEIN GENE (FABP4) TO CHROMOSOME 8Q21 USING SOMATIC-CELL HYBRID AND FLUORESCENCE IN-SITU HYBRIDIZATION TECHNIQUES, Genomics, 40(1), 1997, pp. 207-209
ASSIGNMENT OF THE CANALICULAR MULTISPECIFIC ORGANIC ANION TRANSPORTERGENE (CMOAT) TO HUMAN-CHROMOSOME 10Q24 AND MOUSE-CHROMOSOME 19D2 BY FLUORESCENT IN-SITU HYBRIDIZATION
Authors: VANKUIJCK MA KOOL M MERKX GFM VANKESSEL AG BINDELS RJM DEEN PMT VANOS CH
Citation: Ma. Vankuijck et al., ASSIGNMENT OF THE CANALICULAR MULTISPECIFIC ORGANIC ANION TRANSPORTERGENE (CMOAT) TO HUMAN-CHROMOSOME 10Q24 AND MOUSE-CHROMOSOME 19D2 BY FLUORESCENT IN-SITU HYBRIDIZATION, Cytogenetics and cell genetics, 77(3-4), 1997, pp. 285-287
LINKAGE OF GITELMAN-SYNDROME TO THE THIAZIDE-SODIUM-CHLORIDE COTRANSPORTER GENE WITH IDENTIFICATION OF MUTATIONS IN DUTCH FAMILIES (VOL 10,PG 403, 1996)
Authors: LEMMINK HH VANDENHEUVEL LPWJ VANDIJK HA MERKX GFM SMILDE TJ TASCHNER PEM MONNENS LAH HEBERT SC KNOERS NVAM
Citation: Hh. Lemmink et al., LINKAGE OF GITELMAN-SYNDROME TO THE THIAZIDE-SODIUM-CHLORIDE COTRANSPORTER GENE WITH IDENTIFICATION OF MUTATIONS IN DUTCH FAMILIES (VOL 10,PG 403, 1996), Pediatric nephrology, 10(5), 1996, pp. 1
LINKAGE OF GITELMAN-SYNDROME TO THE THIAZIDE-SENSITIVE SODIUM-CHLORIDE COTRANSPORTER GENE WITH IDENTIFICATION OF MUTATIONS IN DUTCH FAMILIES
Authors: LEMMINK HH VANDENHEUVEL LPWJ VANDIJK HA MERKX GFM SMILDE TJ TASCHNER PEM MONNENS LAH HEBERT SC KNOERS NVAM
Citation: Hh. Lemmink et al., LINKAGE OF GITELMAN-SYNDROME TO THE THIAZIDE-SENSITIVE SODIUM-CHLORIDE COTRANSPORTER GENE WITH IDENTIFICATION OF MUTATIONS IN DUTCH FAMILIES, Pediatric nephrology, 10(4), 1996, pp. 403-407
CDNA CLONING AND CHROMOSOMAL LOCALIZATION OF THE GENES ENCODING THE ALPHA-SUBUNI AND BETA-SUBUNIT OF HUMAN RAB GERANYLGERANYL TRANSFERASE -3'-END OF THE ALPHA-SUBUNIT GENE OVERLAPS WITH THE TRANSGLUTAMINASE-1GENE PROMOTER
Authors: VANBOKHOVEN H RAWSON RB MERKX GFM CREMERS FPM SEABRA MC
Citation: H. Vanbokhoven et al., CDNA CLONING AND CHROMOSOMAL LOCALIZATION OF THE GENES ENCODING THE ALPHA-SUBUNI AND BETA-SUBUNIT OF HUMAN RAB GERANYLGERANYL TRANSFERASE -3'-END OF THE ALPHA-SUBUNIT GENE OVERLAPS WITH THE TRANSGLUTAMINASE-1GENE PROMOTER, Genomics, 38(2), 1996, pp. 133-140
A DUPLICATION PARACENTRIC INVERSION ASSOCIATED WITH FAMILIAL X-LINKEDDEAFNESS (DFN3) SUGGESTS THE PRESENCE OF A REGULATORY ELEMENT MORE THAN 400 KB UPSTREAM OF THE POU3F4 GENE
Authors: DEKOK YJM MERKX GFM VANDERMAAREL SM HUBER I MALCOLM S ROPERS HH CREMERS FPM
Citation: Yjm. Dekok et al., A DUPLICATION PARACENTRIC INVERSION ASSOCIATED WITH FAMILIAL X-LINKEDDEAFNESS (DFN3) SUGGESTS THE PRESENCE OF A REGULATORY ELEMENT MORE THAN 400 KB UPSTREAM OF THE POU3F4 GENE, Human molecular genetics, 4(11), 1995, pp. 2145-2150
ICF SYNDROME - A NEW CASE AND REVIEW OF THE LITERATURE
Authors: SMEETS DFCM MOOG U WEEMAES CMR VAESPEETERS G MERKX GFM NIEHOF JP HAMERS G
Citation: Dfcm. Smeets et al., ICF SYNDROME - A NEW CASE AND REVIEW OF THE LITERATURE, Human genetics, 94(3), 1994, pp. 240-246
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