AAAAAA
Results: 51-75/87
Authors:
OLDRIDGE M
WILKIE AOM
SLANEY SF
POOLE MD
PULLEYN LJ
RUTLAND P
HOCKLEY AD
WAKE MJC
GOLDIN JH
WINTER RM
REARDON W
MALCOLM S
Citation: M. Oldridge et al., MUTATIONS IN THE 3RD IMMUNOGLOBULIN DOMAIN OF THE FIBROBLAST GROWTH-FACTOR RECEPTOR-2 GENE IN CROUZON SYNDROME, Human molecular genetics, 4(6), 1995, pp. 1077-1082
Authors:
WINTER RM
Citation: Rm. Winter, RECENT MOLECULAR ADVANCES IN DYSMORPHOLOGY, Human molecular genetics, 4, 1995, pp. 1699-1704
Authors:
QIAN LL
BRUCE FA
KELLAR JJ
WINTER RM
Citation: Ll. Qian et al., AN INSTRUMENT FOR TESTING INTERFACIAL SHEAR-STRENGTH IN POLYMER MATRIX COMPOSITES, Measurement science & technology, 6(7), 1995, pp. 1009-1015
Authors:
WENSEL RW
PENALOZA M
CROSS WM
WINTER RM
KELLAR JJ
Citation: Rw. Wensel et al., ADSORPTION BEHAVIOR OF OLEATE ON MG(OH)(2) AS REVEALED BY FT-IR SPECTROSCOPY, Langmuir, 11(11), 1995, pp. 4593-4595
Authors:
EVANS CD
WINTER RM
Citation: Cd. Evans et Rm. Winter, A CASE-BASED LEARNING APPROACH, TO GROUPING CASES WITH MULTIPLE MALFORMATIONS, M.D. computing, 12(2), 1995, pp. 127-136
Authors:
ROSE CSP
KING AAJ
YANG S
WILKIE AOM
REARDON W
MALCOLM S
WINTER RM
Citation: Csp. Rose et al., THE LOCALIZATION OF THE GENETIC-LOCUS OF THE SAETHRE-CHOTZEN SYNDROME, Cytogenetics and cell genetics, 71(1), 1995, pp. 27-27
Authors:
REARDON W
GIBBONS RJ
WINTER RM
BARAITSER M
Citation: W. Reardon et al., MALE PSEUDOHERMAPHRODITISM IN SIBS WITH THE ALPHA-THALASSEMIA MENTAL-RETARDATION (ATR-X) SYNDROME, American journal of medical genetics, 55(3), 1995, pp. 285-287
Authors:
ELMSLIE FV
VIVIAN AJ
GARDINER H
HALL C
MOWAT AP
WINTER RM
Citation: Fv. Elmslie et al., ALAGILLE SYNDROME - FAMILY STUDIES, Journal of Medical Genetics, 32(4), 1995, pp. 264-268
SAETHRE-CHOTZEN-SYNDROME ASSOCIATED WITH BALANCED TRANSLOCATIONS INVOLVING 7P21 - 3 FURTHER FAMILIES
Authors:
WILKIE AOM
YANG SP
SUMMERS D
POOLE MD
REARDON W
WINTER RM
Citation: Aom. Wilkie et al., SAETHRE-CHOTZEN-SYNDROME ASSOCIATED WITH BALANCED TRANSLOCATIONS INVOLVING 7P21 - 3 FURTHER FAMILIES, Journal of Medical Genetics, 32(3), 1995, pp. 174-180
Authors:
ELMSLIE FV
VIVIAN AJ
BAKER A
MOWAT AP
WINTER RM
Citation: Fv. Elmslie et al., ALAGILLE SYNDROME - IS THE FACE SPECIFIC, Journal of Medical Genetics, 32(2), 1995, pp. 148-148
Authors:
MUENKE M
SCHELL U
HEHR A
ROBIN NH
LOSKEN HW
SCHINZEL A
PULLEYN LJ
RUTLAND P
REARDON W
MALCOLM S
WINTER RM
Citation: M. Muenke et al., A COMMON MUTATION IN THE FIBROBLAST GROWTH-FACTOR RECEPTOR-1 GENE IN PFEIFFER-SYNDROME, Nature genetics, 8(3), 1994, pp. 269-274
Authors:
REARDON W
WINTER RM
RUTLAND P
PULLEYN LJ
JONES BM
MALCOLM S
Citation: W. Reardon et al., MUTATIONS IN THE FIBROBLAST GROWTH-FACTOR RECEPTOR-2 GENE CAUSE CROUZON-SYNDROME, Nature genetics, 8(1), 1994, pp. 98-103
Authors:
VITS L
VANCAMP G
COUCKE P
FRANSEN E
DEBOULLE K
REYNIERS E
KORN B
POUSTKA A
WILSON G
SCHRANDERSTUMPEL C
WINTER RM
SCHWARTZ C
WILLEMS PJ
Citation: L. Vits et al., MASA SYNDROME IS DUE TO MUTATIONS IN THE NEURAL CELL-ADHESION GENE L1CAM, Nature genetics, 7(3), 1994, pp. 408-413
Authors:
ROSE CSP
KING AAJ
SUMMERS D
PALMER R
YANG S
WILKIE AOM
REARDON W
MALCOLM S
WINTER RM
Citation: Csp. Rose et al., LOCALIZATION OF THE GENETIC-LOCUS FOR SAETHRE-CHOTZEN-SYNDROME TO A 6CM REGION OF CHROMOSOME-7 USING 4 CASES WITH APPARENTLY BALANCED TRANSLOCATIONS AT 7P21.2, Human molecular genetics, 3(8), 1994, pp. 1405-1408
Authors:
ROBIN NH
FELDMAN GJ
MITCHELL HF
LORENZ P
WILROY RS
ZACKAI EH
ALLANSON JE
REICH EW
PFEIFFER RA
CLARKE LA
WARMAN ML
MULLIKEN JB
BRUETON LA
WINTER RM
PRICE RA
GASSER DL
MUENKE M
Citation: Nh. Robin et al., LINKAGE OF PFEIFFER-SYNDROME TO CHROMOSOME-8 CENTROMERE AND EVIDENCE FOR GENETIC-HETEROGENEITY, Human molecular genetics, 3(12), 1994, pp. 2153-2158
Authors:
ROSE CSP
VANHERWERDEN L
REARDON W
BRUETON LA
MALCOLM S
WINTER RM
Citation: Csp. Rose et al., MAPPING OF SAETHRE-CHOTZEN SYNDROME (ACSIII) ON 7P, Cytogenetics and cell genetics, 65(1-2), 1994, pp. 69-69
Authors:
REARDON W
BOYD S
PITT MC
WILSON J
WINTER RM
Citation: W. Reardon et al., DISORDERED PERIPHERAL-NERVE CONDUCTION IN DOOR(S) SYNDROME, Neuropediatrics, 25(1), 1994, pp. 33-35
NEW AUTOSOMAL-DOMINANT FORM OF SPONDYLOEPIPHYSEAL DYSPLASIA PRESENTING WITH ATLANTOAXIAL INSTABILITY
Authors:
REARDON W
HALL CM
SHAW DG
KENDALL B
HAYWARD R
WINTER RM
Citation: W. Reardon et al., NEW AUTOSOMAL-DOMINANT FORM OF SPONDYLOEPIPHYSEAL DYSPLASIA PRESENTING WITH ATLANTOAXIAL INSTABILITY, American journal of medical genetics, 52(4), 1994, pp. 432-437
Authors:
CHOTAI KA
BRUETON LA
VANHERWERDEN L
GARRETT C
HINKEL GK
SCHINZEL A
MUELLER RF
SPELEMAN F
WINTER RM
Citation: Ka. Chotai et al., 6 CASES OF 7P DELETION - CLINICAL, CYTOGENETIC, AND MOLECULAR STUDIES, American journal of medical genetics, 51(3), 1994, pp. 270-276
Authors:
WINTER RM
Citation: Rm. Winter, PFEIFFER SYNDROME, American journal of medical genetics, 49(3), 1994, pp. 357-357
Authors:
REARDON W
WINTER RM
Citation: W. Reardon et Rm. Winter, SAETHRE-CHOTZEN SYNDROME, Journal of Medical Genetics, 31(5), 1994, pp. 393-396
Authors:
REARDON W
VANHERWERDEN L
ROSE C
JONES B
MALCOLM S
WINTER RM
Citation: W. Reardon et al., CROUZON SYNDROME IS NOT LINKED TO CRANIOSYNOSTOSIS LOCI AT 7P AND 5QTER, Journal of Medical Genetics, 31(3), 1994, pp. 219-221
Authors:
ELMSLIE FV
WARD H
CRAUFURD D
STEWART A
WINTER RM
Citation: Fv. Elmslie et al., THE READ CODES IN CLINICAL GENETICS, Journal of Medical Genetics, 31(2), 1994, pp. 166-167
Authors:
WINTER RM
MALLEPALLI RR
HELLEM KP
SZYDLO SW
Citation: Rm. Winter et al., DETERMINATION OF AS, CD, CR, AND PB SPECIES FORMED IN A COMBUSTION ENVIRONMENT, Combustion science and technology, 101(1-6), 1994, pp. 45-58
Authors:
FENG HS
SASSANI R
BARTLETT SP
LEE A
HECHT JT
MALCOLM S
WINTER RM
VINTINER GM
BUETOW KH
GASSER DL
Citation: Hs. Feng et al., EVIDENCE, FROM FAMILY STUDIES, FOR LINKAGE DISEQUILIBRIUM BETWEEN TGFA AND A GENE FOR NONSYNDROMIC CLEFT-LIP WITH OR WITHOUT CLEFT-PALATE, American journal of human genetics, 55(5), 1994, pp. 932-936