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Results: 1-12 |
Results: 12
IDENTIFICATION OF A 3RD EXT-LIKE GENE (EXTL3) BELONGING TO THE EXT GENE FAMILY
Authors: VANHUL W WUYTS W HENDRICKX J SPELEMAN F WAUTERS J DEBOULLE K VANROY N BOSSUYT P WILLEMS PJ
Citation: W. Vanhul et al., IDENTIFICATION OF A 3RD EXT-LIKE GENE (EXTL3) BELONGING TO THE EXT GENE FAMILY, Genomics, 47(2), 1998, pp. 230-237
MUTATIONS IN THE EXT1 AND EXT2 GENES IN HEREDITARY MULTIPLE EXOSTOSES
Authors: WUYTS W VANHUL W DEBOULLE K HENDRICKX J BAKKER E VANHOENACKER F MOLLICA F LUDECKE HJ SAYLI BS PAZZAGLIA UE MORTIER G HAMEL B CONRAD EU MATSUSHITA M RASKIND WH WILLEMS PJ
Citation: W. Wuyts et al., MUTATIONS IN THE EXT1 AND EXT2 GENES IN HEREDITARY MULTIPLE EXOSTOSES, American journal of human genetics, 62(2), 1998, pp. 346-354
IDENTIFICATION AND CHARACTERIZATION OF A NOVEL MEMBER OF THE EXT GENEFAMILY, EXTL2
Authors: WUYTS W VANHUL W HENDRICKX J SPELEMAN F WAUTERS J DEBOULLE K VANROY N VANAGTMAEL T BOSSUYT P WILLEMS PJ
Citation: W. Wuyts et al., IDENTIFICATION AND CHARACTERIZATION OF A NOVEL MEMBER OF THE EXT GENEFAMILY, EXTL2, European journal of human genetics, 5(6), 1997, pp. 382-389
IDENTIFICATION OF THE EXT2 GENE ASSOCIATED WITH HEREDITARY MULTIPLE EXOSTOSES, AND 3 OTHER MEMBERS FROM THIS NOVEL GENE FAMILY
Authors: VANHUL W WUYTS W HENDRICKX J WAUTERS J DEBOULLE K WILLEMS PJ
Citation: W. Vanhul et al., IDENTIFICATION OF THE EXT2 GENE ASSOCIATED WITH HEREDITARY MULTIPLE EXOSTOSES, AND 3 OTHER MEMBERS FROM THIS NOVEL GENE FAMILY, Journal of bone and mineral research, 12, 1997, pp. 661-661
DEFECT-11 SYNDROME - REPORT OF A NEW FAMILY WITH UNUSUAL NEUROLOGICALMANIFESTATIONS
Authors: CASALI C WUYTS W DIGENNARO G VANHUL W FORTINI D SPADARO M PIERELLI F WILLEMS P MOROCUTTI C
Citation: C. Casali et al., DEFECT-11 SYNDROME - REPORT OF A NEW FAMILY WITH UNUSUAL NEUROLOGICALMANIFESTATIONS, American journal of human genetics, 61(4), 1997, pp. 518-518
IDENTIFICATION OF A NEW FAMILY OF EXT-RELATED GENES
Authors: WUYTS W VANHUL W HENDRICKX J DEBOULLE K WILLEMS PW
Citation: W. Wuyts et al., IDENTIFICATION OF A NEW FAMILY OF EXT-RELATED GENES, American journal of human genetics, 61(4), 1997, pp. 2059-2059
LOCALIZATION OF A GENE FOR AUTOSOMAL-DOMINANT OSTEOPETROSIS (ALBERS-SCHONBERG-DISEASE) TO CHROMOSOME 1P21
Authors: VANHUL W BOLLERSLEV J GRAM J VANHUL E WUYTS W BENICHOU O VANHOENACKER F WILLEMS PJ
Citation: W. Vanhul et al., LOCALIZATION OF A GENE FOR AUTOSOMAL-DOMINANT OSTEOPETROSIS (ALBERS-SCHONBERG-DISEASE) TO CHROMOSOME 1P21, American journal of human genetics, 61(2), 1997, pp. 363-369
POSITIONAL CLONING OF A GENE INVOLVED IN HEREDITARY MULTIPLE EXOSTOSES
Authors: WUYTS W VANHUL W WAUTERS J NEMTSOVA M REYNIERS E VANHUL E DEBOULLE K DEVRIES BBA HENDRICKX J HERRYGERS I BOSSUYT P BALEMANS W FRANSEN E VITS L COUCKE P NOWAK NJ SHOWS TB MALLET L VANDENOUWELAND AMW MCGAUGHRAN J HALLEY DJJ WILLEMS PJ
Citation: W. Wuyts et al., POSITIONAL CLONING OF A GENE INVOLVED IN HEREDITARY MULTIPLE EXOSTOSES, Human molecular genetics, 5(10), 1996, pp. 1547-1557
DELINEATION OF A CONTIGUOUS GENE SYNDROME WITH MULTIPLE EXOSTOSES, ENLARGED PARIETAL FORAMINA, CRANIOFACIAL DYSOSTOSIS, AND MENTAL-RETARDATION, CAUSED BY DELETIONS ON THE SHORT ARM OF CHROMOSOME-11
Authors: BARTSCH O WUYTS W VANHUL W HECHT JT MEINECKE P HOGUE D WERNER W ZABEL B HINKEL GK POWELL CM SHAFFER LG WILLEMS PJ
Citation: O. Bartsch et al., DELINEATION OF A CONTIGUOUS GENE SYNDROME WITH MULTIPLE EXOSTOSES, ENLARGED PARIETAL FORAMINA, CRANIOFACIAL DYSOSTOSIS, AND MENTAL-RETARDATION, CAUSED BY DELETIONS ON THE SHORT ARM OF CHROMOSOME-11, American journal of human genetics, 58(4), 1996, pp. 734-742
MOLECULAR DELINEATION OF A NEW CONTIGUOUS GENE SYNDROME WITH MULTIPLEEXOSTOSES ASSOCIATED WITH DELETIONS ON THE SHORT ARM OF CHROMOSOME-11
Authors: VANHUL W WUYTS W HECHT JT BARTSCH O MEINECKE P ZABEL B WERNER W HINKEL GK WILLEMS P
Citation: W. Vanhul et al., MOLECULAR DELINEATION OF A NEW CONTIGUOUS GENE SYNDROME WITH MULTIPLEEXOSTOSES ASSOCIATED WITH DELETIONS ON THE SHORT ARM OF CHROMOSOME-11, American journal of human genetics, 57(4), 1995, pp. 31-31
CLINICAL DESCRIPTION OF A NEW CONTIGUOUS GENE SYNDROME OF CHROMOSOME 11P WITH MULTIPLE EXOSTOSES, ENLARGED PARIETAL FORAMINA, MICROPENIS, AND MENTAL-RETARDATION
Authors: BARTSCH O HINKEL GK WERNER W MEINECKE P WUYTS W VANHUL W WILLEMS PJ
Citation: O. Bartsch et al., CLINICAL DESCRIPTION OF A NEW CONTIGUOUS GENE SYNDROME OF CHROMOSOME 11P WITH MULTIPLE EXOSTOSES, ENLARGED PARIETAL FORAMINA, MICROPENIS, AND MENTAL-RETARDATION, American journal of human genetics, 57(4), 1995, pp. 275-275
REFINEMENT OF THE MULTIPLE EXOSTOSES LOCUS (EXT2) TO A 3-CM INTERVAL ON CHROMOSOME-11
Authors: WUYTS W RAMLAKHAN S VANHUL W HECHT JT VANDENOUWELAND AMW RASKIND WH HOFSTEDE FC REYNIERS E WELLS DE DEVRIES B CONRAD EU HILL A ZALATAYEV D WEISSENBACH J WAGNER MJ BAKKER E HALLEY DJJ WILLEMS PJ
Citation: W. Wuyts et al., REFINEMENT OF THE MULTIPLE EXOSTOSES LOCUS (EXT2) TO A 3-CM INTERVAL ON CHROMOSOME-11, American journal of human genetics, 57(2), 1995, pp. 382-387
Risultati: 1-12 |