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Results:
1-21
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Results: 21
Authors:
MULLEY J
SAAR K
HEWITT G
RUSCHENDORF F
PHILLIPS H
COLLEY A
SILLENCE D
REIS A
WILSON M
Citation: J. Mulley et al., GENE LOCALIZATION FOR AN AUTOSOMAL-DOMINANT FAMILIAL PERIODIC FEVER TO 12P13, American journal of human genetics, 62(4), 1998, pp. 884-889
Authors:
WORTHINGTON S
COLLEY A
FAGAN K
DAI K
LIPSON AH
Citation: S. Worthington et al., ANAL ANOMALIES - AN UNCOMMON FEATURE OF VELOCARDIOFACIAL (SHPRINTZEN)SYNDROME, Journal of Medical Genetics, 34(1), 1997, pp. 79-82
Authors:
COMBER C
COLLEY A
HARGREAVES DJ
DORN L
Citation: C. Comber et al., THE EFFECTS OF AGE, GENDER AND COMPUTER EXPERIENCE UPON COMPUTER ATTITUDES, Educational research, 39(2), 1997, pp. 123-133
Authors:
MULLEY J
SAAR K
HEWITT G
RUSCHENDORF F
PHILLIPS H
COLLEY A
SILLENCE D
REIS A
WILSON M
Citation: J. Mulley et al., GENE LOCALIZATION FOR AN AUTOSOMAL-DOMINANT FAMILIAL PERIODIC FEVER, American journal of human genetics, 61(4), 1997, pp. 1672-1672
Authors:
DONNELLY A
COLLEY A
CRIMMINS D
MULLEY J
Citation: A. Donnelly et al., A NOVEL MUTATION IN EXON-6 (F236S) OF THE PROTEOLIPID PROTEIN GENE ISASSOCIATED WITH SPASTIC PARAPLEGIA, Human mutation, 8(4), 1996, pp. 384-385
Authors:
COLLEY A
HENRY O
HOLMES S
JAMES L
Citation: A. Colley et al., PERCEPTIONS OF ABILITY TO PROGRAM OR TO USE A WORD-PROCESSOR, Computers in human behavior, 12(3), 1996, pp. 329-337
Authors:
COLLEY A
GRIFFITH D
HUGH M
LANDERS K
JAGGLI N
Citation: A. Colley et al., CHILDHOOD PLAY AND ADOLESCENT LEISURE PREFERENCES - ASSOCIATIONS WITHGENDER TYPING AND THE PRESENCE OF SIBLINGS, Sex roles, 35(3-4), 1996, pp. 233-245
Authors:
LIPSON A
FAGAN K
COLLEY A
COLLEY P
SHOLLER G
ISSACS D
OATES RK
Citation: A. Lipson et al., VELO-CARDIO-FACIAL AND PARTIAL DIGEORGE PHENOTYPE IN A CHILD WITH INTERSTITIAL DELETION AT 10P13 - IMPLICATIONS FOR CYTOGENETICS AND MOLECULAR-BIOLOGY, American journal of medical genetics, 65(4), 1996, pp. 304-308
Authors:
SMITH A
WILES C
HAAN E
MCGILL J
WALLACE G
DIXON J
SELBY R
COLLEY A
MARKS R
TRENT RJ
Citation: A. Smith et al., CLINICAL-FEATURES IN 27 PATIENTS WITH ANGELMAN SYNDROME RESULTING FROM DNA DELETION, Journal of Medical Genetics, 33(2), 1996, pp. 107-112
Authors:
COLLEY A
DONNAI D
EVANS DGR
Citation: A. Colley et al., NEUROFIBROMATOSIS NOONAN PHENOTYPE - A VARIABLE FEATURE OF TYPE-1 NEUROFIBROMATOSIS, Clinical genetics, 49(2), 1996, pp. 59-64
Authors:
COLLEY A
Citation: A. Colley, PSYCHOLOGY, SCIENCE AND WOMEN, Psychologist, 8(8), 1995, pp. 346-352
Authors:
LINDSAY G
COLLEY A
Citation: G. Lindsay et A. Colley, ETHICAL DILEMMAS OF MEMBERS OF THE SOCIETY, Psychologist, 8(10), 1995, pp. 448-451
Authors:
COLLEY A
HILL F
HILL J
JONES A
Citation: A. Colley et al., GENDER EFFECTS IN THE STEREOTYPING OF THOSE WITH DIFFERENT KINDS OF COMPUTING EXPERIENCE, Journal of educational computing research, 12(1), 1995, pp. 19-27
Authors:
HARGREAVES DJ
COMBER C
COLLEY A
Citation: Dj. Hargreaves et al., EFFECTS OF AGE, GENDER, AND TRAINING ON MUSICAL PREFERENCES OF BRITISH SECONDARY-SCHOOL STUDENTS, Journal of research in music education, 43(3), 1995, pp. 242-250
Authors:
COLLEY A
COMBER C
HARGREAVES DJ
Citation: A. Colley et al., SCHOLL SUBJECT PREFERENCES OF PUPILS IN SINGLE-SEX AND CO-EDUCATIONALSECONDARY-SCHOOLS, Educational studies, 20(3), 1994, pp. 379-385
Authors:
COLLEY A
COMBER C
HARGREAVES DJ
Citation: A. Colley et al., GENDER EFFECTS IN SCHOOL SUBJECT PREFERENCES - A RESEARCH NOTE, Educational studies, 20(1), 1994, pp. 13-18
Authors:
FAGAN K
KENNEDY C
RODDICK L
COLLEY A
Citation: K. Fagan et al., AN INTERSTITIAL DELETION OF CHROMOSOME 7(Q35), Journal of Medical Genetics, 31(9), 1994, pp. 738-739
Authors:
COLLEY A
Citation: A. Colley, SCIENCE IN SCHOOLS, New scientist, 140(1905-6), 1993, pp. 68-68
Authors:
BENJAMIN CM
COLLEY A
DONNAI D
KINGSTON H
HARRIS R
KERZINSTORRAR L
Citation: Cm. Benjamin et al., NEUROFIBROMATOSIS TYPE-1 (NF1) - KNOWLEDGE, EXPERIENCE, AND REPRODUCTIVE DECISIONS OF AFFECTED PATIENTS AND FAMILIES, Journal of Medical Genetics, 30(7), 1993, pp. 567-574
Authors:
LLOYD IC
COLLEY A
TULLO AB
BONSHEK R
Citation: Ic. Lloyd et al., DOMINANTLY INHERITED UNILATERAL RETINAL DYSPLASIA, British journal of ophthalmology, 77(6), 1993, pp. 378-380
Authors:
TASSABEHJI M
STRACHAN T
SHARLAND M
COLLEY A
DONNAI D
HARRIS R
THAKKER N
Citation: M. Tassabehji et al., TANDEM DUPLICATION WITHIN A NEUROFIBROMATOSIS TYPE-I (NF1) GENE EXON IN A FAMILY WITH FEATURES OF WATSON SYNDROME AND NOONAN SYNDROME, American journal of human genetics, 53(1), 1993, pp. 90-95
Risultati:
1-21
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