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Results: 1-7 |
Results: 7
GENES IN CRANIOSYNOSTOSIS
Authors: WILKIE A JOHNSON D HORSLEY SW KEARNEY L KUNZ J MOLONEY DM OLDRIDGE M TWIGG SRF WALSH S ZACKAI EH
Citation: A. Wilkie et al., GENES IN CRANIOSYNOSTOSIS, European journal of human genetics, 6, 1998, pp. 28-28
A COMPREHENSIVE SCREEN FOR TWIST MUTATIONS IN PATIENTS WITH CRANIOSYNOSTOSIS IDENTIFIES A NEW MICRODELETION SYNDROME OF CHROMOSOME BAND 7P21.1
Authors: JOHNSON D HORSLEY SW MOLONEY DM OLDRIDGE M TWIGG SRF WALSH S BARROW M NJOLSTAD PR KUNZ J ASHWORTH GJ WALL SA KEARNEY L WILKIE AOM
Citation: D. Johnson et al., A COMPREHENSIVE SCREEN FOR TWIST MUTATIONS IN PATIENTS WITH CRANIOSYNOSTOSIS IDENTIFIES A NEW MICRODELETION SYNDROME OF CHROMOSOME BAND 7P21.1, American journal of human genetics, 63(5), 1998, pp. 1282-1293
GENOTYPE-PHENOTYPE CORRELATION FOR NUCLEOTIDE SUBSTITUTIONS IN THE IGII-IGIII LINKER OF FGFR2
Authors: OLDRIDGE M LUNT PW ZACKAI EH MCDONALDMCGINN DM MUENKE M MOLONEY DM TWIGG SRF HEATH JK HOWARD TD HOGANSON G GAGNON DM JABS EW WILKIE AOM
Citation: M. Oldridge et al., GENOTYPE-PHENOTYPE CORRELATION FOR NUCLEOTIDE SUBSTITUTIONS IN THE IGII-IGIII LINKER OF FGFR2, Human molecular genetics, 6(1), 1997, pp. 137-143
PREVALENCE OF PRO250ARG MUTATION OF FIBROBLAST GROWTH-FACTOR RECEPTOR-3 IN CORONAL CRANIOSYNOSTOSIS
Authors: MOLONEY DM WALL SA ASHWORTH GJ OLDRIDGE M GLASS IA FRANCOMANO CA MUENKE M WILKIE AOM
Citation: Dm. Moloney et al., PREVALENCE OF PRO250ARG MUTATION OF FIBROBLAST GROWTH-FACTOR RECEPTOR-3 IN CORONAL CRANIOSYNOSTOSIS, Lancet, 349(9058), 1997, pp. 1059-1062
A UNIQUE POINT MUTATION IN THE FIBROBLAST-GROWTH-FACTOR-RECEPTOR-3 GENE (FGFR3) DEFINES A NEW CRANIOSYNOSTOSIS SYNDROME
Authors: MUENKE M GRIPP KW MCDONALDMCGINN DM GAUDENZ K WHITAKER LA BARTLETT SP MARKOWITZ RI ROBIN NH NWOKORO N MULVIHILL JJ LOSKEN HW MULLIKEN JB GUTTMACHER AE WILROY RS CLARKE LA HOLLWAY G ADES LC HAAN EA MULLEY JC COHEN MM BELLUS GA FRANCOMANO CA MOLONEY DM WALL SA WILKIE AOM ZACKAI EH
Citation: M. Muenke et al., A UNIQUE POINT MUTATION IN THE FIBROBLAST-GROWTH-FACTOR-RECEPTOR-3 GENE (FGFR3) DEFINES A NEW CRANIOSYNOSTOSIS SYNDROME, American journal of human genetics, 60(3), 1997, pp. 555-564
EXCLUSIVE PATERNAL ORIGIN OF NEW MUTATIONS IN APERT SYNDROME
Authors: MOLONEY DM SLANEY SF OLDRIDGE M WALL SA SAHLIN P STENMAN G WILKIE AOM
Citation: Dm. Moloney et al., EXCLUSIVE PATERNAL ORIGIN OF NEW MUTATIONS IN APERT SYNDROME, Nature genetics, 13(1), 1996, pp. 48-53
RECURRENCE OF THIN MELANOMA - HOW EFFECTIVE IS FOLLOW-UP
Authors: MOLONEY DM GORDON DJ BRIGGS JC RIGBY HS
Citation: Dm. Moloney et al., RECURRENCE OF THIN MELANOMA - HOW EFFECTIVE IS FOLLOW-UP, British Journal of Plastic Surgery, 49(6), 1996, pp. 409-413
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