AAAAAA

   
Results: 1-17 |
Results: 17
FMR2 EXPRESSION IN FAMILIES WITH FRAXE MENTAL-RETARDATION
Authors: GECZ J OOSTRA BA HOCKEY A CARBONELL P TURNER G HAAN EA SUTHERLAND GR MULLEY JC
Citation: J. Gecz et al., FMR2 EXPRESSION IN FAMILIES WITH FRAXE MENTAL-RETARDATION, Human molecular genetics, 6(3), 1997, pp. 435-441
GENE STRUCTURE AND SUBCELLULAR-LOCALIZATION OF FMR2, A MEMBER OF A NEW FAMILY OF PUTATIVE TRANSCRIPTION ACTIVATORS
Authors: GECZ J BIELBY S SUTHERLAND GR MULLEY JC
Citation: J. Gecz et al., GENE STRUCTURE AND SUBCELLULAR-LOCALIZATION OF FMR2, A MEMBER OF A NEW FAMILY OF PUTATIVE TRANSCRIPTION ACTIVATORS, Genomics, 44(2), 1997, pp. 201-213
MUTATION DETECTION IN FGFR2 CRANIOSYNOSTOSIS SYNDROMES
Authors: HOLLWAY GE SUTHERS GK HAAN EA THOMPSON E DAVID DJ GECZ J MULLEY JC
Citation: Ge. Hollway et al., MUTATION DETECTION IN FGFR2 CRANIOSYNOSTOSIS SYNDROMES, Human genetics, 99(2), 1997, pp. 251-255
IDENTIFICATION OF THE GENE FMR2, ASSOCIATED WITH FRAXE MENTAL-RETARDATION
Authors: GECZ J GEDEON AK SUTHERLAND GR MULLEY JC
Citation: J. Gecz et al., IDENTIFICATION OF THE GENE FMR2, ASSOCIATED WITH FRAXE MENTAL-RETARDATION, Nature genetics, 13(1), 1996, pp. 105-108
XNP MUTATION IN A LARGE FAMILY WITH JUBERG-MARSIDI SYNDROME
Authors: VILLARD L GECZ J MATTEI JF FONTES M SAUGIERVEBER P MUNNICH A LYONNET S
Citation: L. Villard et al., XNP MUTATION IN A LARGE FAMILY WITH JUBERG-MARSIDI SYNDROME, Nature genetics, 12(4), 1996, pp. 359-360
SPLICING MUTATION IN THE ATR-X GENE CAN LEAD TO A DYSMORPHIC MENTAL-RETARDATION PHENOTYPE WITHOUT ALPHA-THALASSEMIA
Authors: VILLARD L TOUTAIN A LOSSI AM GECZ J HOUDAYER C MORAINE C FONTES M
Citation: L. Villard et al., SPLICING MUTATION IN THE ATR-X GENE CAN LEAD TO A DYSMORPHIC MENTAL-RETARDATION PHENOTYPE WITHOUT ALPHA-THALASSEMIA, American journal of human genetics, 58(3), 1996, pp. 499-505
CONSTRUCTION OF A YAC CONTIG SPANNING THE XQ13.3 SUBBAND
Authors: VILLARD L GECZ J COLLEAUX L LOSSI AM CHELLY J ISHIKAWABRUSH Y MONACO AP FONTES M
Citation: L. Villard et al., CONSTRUCTION OF A YAC CONTIG SPANNING THE XQ13.3 SUBBAND, Genomics, 26(1), 1995, pp. 115-122
ASSIGNMENT OF A POLYCOMB-LIKE CHROMOBOX GENE (CBX2) TO HUMAN-CHROMOSOME 17Q25
Authors: GECZ J GAUNT SJ PASSAGE E BURTON RD CUDREY C PEARCE JJH FONTES M
Citation: J. Gecz et al., ASSIGNMENT OF A POLYCOMB-LIKE CHROMOBOX GENE (CBX2) TO HUMAN-CHROMOSOME 17Q25, Genomics, 26(1), 1995, pp. 130-133
OVERLAPPING SUBMICROSCOPIC DELETIONS IN XQ28 IN 2 UNRELATED BOYS WITHDEVELOPMENTAL DISORDERS - IDENTIFICATION OF A GENE NEAR FRAXE
Authors: GEDEON AK KEINANEN M ADES LC KAARIAINEN H GECZ J BAKER E SUTHERLAND GR MULLEY JC
Citation: Ak. Gedeon et al., OVERLAPPING SUBMICROSCOPIC DELETIONS IN XQ28 IN 2 UNRELATED BOYS WITHDEVELOPMENTAL DISORDERS - IDENTIFICATION OF A GENE NEAR FRAXE, American journal of human genetics, 56(4), 1995, pp. 907-914
CLONING AND CHARACTERIZATION OF A NEW HUMAN XQ13 GENE, ENCODING A PUTATIVE HELICASE
Authors: STAYTON CL DABOVIC B GULISANO M GECZ J BROCCOLI V GIOVANAZZI S BOSSOLASCO M MONACO L RASTAN S BONCINELLI E BIANCHI ME CONSALEZ GG
Citation: Cl. Stayton et al., CLONING AND CHARACTERIZATION OF A NEW HUMAN XQ13 GENE, ENCODING A PUTATIVE HELICASE, Human molecular genetics, 3(11), 1994, pp. 1957-1964
CLONING AND EXPRESSION OF THE MURINE HOMOLOG OF A PUTATIVE HUMAN X-LINKED NUCLEAR-PROTEIN GENE CLOSELY LINKED TO PGK1 IN XQ13.3
Authors: GECZ J POLLARD H CONSALEZ G VILLARD L STAYTON C MILLASSEAU P KHRESTCHATISKY M FONTES M
Citation: J. Gecz et al., CLONING AND EXPRESSION OF THE MURINE HOMOLOG OF A PUTATIVE HUMAN X-LINKED NUCLEAR-PROTEIN GENE CLOSELY LINKED TO PGK1 IN XQ13.3, Human molecular genetics, 3(1), 1994, pp. 39-44
PHYSICAL AND TRANSCRIPTIONAL MAPPING IN THE XQ12-]Q21 REGION
Authors: VILLARD L GECZ J COLLEAUX L LOSSI AM FONTES M
Citation: L. Villard et al., PHYSICAL AND TRANSCRIPTIONAL MAPPING IN THE XQ12-]Q21 REGION, Cytogenetics and cell genetics, 67(4), 1994, pp. 337-337
HYBRID SELECTION USING HUMAN AND MOUSE CDNAS - APPLICATION TO DXS56-PGK1 REGION IN XQ13.3
Authors: GECZ J VILLARD L LOSSI AM FONTES M
Citation: J. Gecz et al., HYBRID SELECTION USING HUMAN AND MOUSE CDNAS - APPLICATION TO DXS56-PGK1 REGION IN XQ13.3, Cytogenetics and cell genetics, 67(4), 1994, pp. 338-338
PHYSICAL AND TRANSCRIPTIONAL MAPPING OF DXS56-PGK1 1-MB REGION - IDENTIFICATION OF 3 NEW TRANSCRIPTS
Authors: GECZ J VILLARD L LOSSI AM MILLASSEAU P DJABALI M FONTES M
Citation: J. Gecz et al., PHYSICAL AND TRANSCRIPTIONAL MAPPING OF DXS56-PGK1 1-MB REGION - IDENTIFICATION OF 3 NEW TRANSCRIPTS, Human molecular genetics, 2(9), 1993, pp. 1389-1396
PROGRESS TOWARD THE CONSTRUCTION OF A YAC CONTIG COVERING THE WHOLE XQ13.3 SUBBAND
Authors: VILLARD L GECZ J LOSSI AM FONTES M
Citation: L. Villard et al., PROGRESS TOWARD THE CONSTRUCTION OF A YAC CONTIG COVERING THE WHOLE XQ13.3 SUBBAND, Cytogenetics and cell genetics, 64(3-4), 1993, pp. 177-177
CONSTRUCTION OF A TRANSCRIPTIONAL MAP OF THE DXS56-PGK1 1-MB REGION VIA DIRECT CDNA SELECTION APPROACH
Authors: GECZ J VILLARD L LOSSI AM FONTES M
Citation: J. Gecz et al., CONSTRUCTION OF A TRANSCRIPTIONAL MAP OF THE DXS56-PGK1 1-MB REGION VIA DIRECT CDNA SELECTION APPROACH, Cytogenetics and cell genetics, 64(3-4), 1993, pp. 178-178
TAQI DIGESTION OF PCR PRODUCT INCREASES THE INFORMATIVITY OF ST14 VNTR FOR THE DIAGNOSIS OF HEMOPHILIA-A
Authors: SAKSOVA L GECZ J KADASI L FERAK V
Citation: L. Saksova et al., TAQI DIGESTION OF PCR PRODUCT INCREASES THE INFORMATIVITY OF ST14 VNTR FOR THE DIAGNOSIS OF HEMOPHILIA-A, Disease markers, 11(2-3), 1993, pp. 139-141
Risultati: 1-17 |