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Results: 1-21 |
Results: 21

Authors: BOUZYK M BRYANT SP EVANS C GUIOLI S FORD S SCHMIDT K GOODFELLOW PN POVEY S REBELLO M ROUSSEAUX S SPURR NK
Citation: M. Bouzyk et al., INTEGRATED RADIATION HYBRID AND YEAST ARTIFICIAL CHROMOSOME MAP OF CHROMOSOME 9P, European journal of human genetics, 5(5), 1997, pp. 299-307

Authors: DECKERT J NOTHEN MM BRYANT SP SCHUFFENHAUER S SCHOFIELD PR SPURR NK PROPPING P
Citation: J. Deckert et al., MAPPING OF THE HUMAN ADENOSINE-A(2A) RECEPTOR GENE - RELATIONSHIP TO POTENTIAL SCHIZOPHRENIA LOCI ON CHROMOSOME 22Q AND EXCLUSION FROM THE CATCH-22 REGION, Human genetics, 99(3), 1997, pp. 326-328

Authors: SHIMRONABARBANELL D ERDMANN J VOGT IR BRYANT SP SPURR NK KNAPP M PROPPING P NOTHEN MM
Citation: D. Shimronabarbanell et al., HUMAN 5-HT5A RECEPTOR GENE - SYSTEMATIC SCREENING FOR DNA-SEQUENCE VARIATION AND LINKAGE MAPPING ON CHROMOSOME 7Q34-Q36 USING A POLYMORPHISM IN THE 5'-UNTRANSLATED REGION, Biochemical and biophysical research communications, 233(1), 1997, pp. 6-9

Authors: JOHNSTON RL BURDON MA SPALTON DJ BRYANT SP BEHNAM JT SELLER MJ
Citation: Rl. Johnston et al., DOMINANT OPTIC ATROPHY, KJER TYPE - LINKAGE ANALYSIS AND CLINICAL-FEATURES IN A LARGE BRITISH PEDIGREE (VOL 115, PG 100, 1997), Archives of ophthalmology, 115(5), 1997, pp. 681-681

Authors: JOHNSTON RL BURDON MA SPALTON DJ BRYANT SP BEHNAM JT SELLER MJ
Citation: Rl. Johnston et al., DOMINANT OPTIC ATROPHY, KJER TYPE - LINKAGE ANALYSIS AND CLINICAL-FEATURES IN A LARGE BRITISH PEDIGREE, Archives of ophthalmology, 115(1), 1997, pp. 100-103

Authors: BOUZYK M BRYANT SP EVANS C GUIOLI S FORD S LAGUDA B SCHMIDT K GOODFELLOW PN EKONG R ROUSSEAUX S SPURR NK
Citation: M. Bouzyk et al., INTEGRATED RADIATION HYBRID AND YAC MAP OF CHROMOSOME 9P, Annals of Human Genetics, 61, 1997, pp. 208-209

Authors: SMITH FJD EADY RAJ LEIGH IM MCMILLAN JR RUGG EL KELSELL DP BRYANT SP SPURR NK GEDDES JF KIRTSCHIG G MILANA G DEBONO AG OWARIBE K WICHE G PULKKINEN L UITTO J MCLEAN WHI LANE EB
Citation: Fjd. Smith et al., PLECTIN DEFICIENCY RESULTS IN MUSCULAR-DYSTROPHY WITH EPIDERMOLYSIS-BULLOSA, Nature genetics, 13(4), 1996, pp. 450-457

Authors: EVANS C BOUZYK M COX S WARNE D BRYANT SP SPURR NK
Citation: C. Evans et al., CHROMOSOMAL ASSIGNMENT OF 79 CDNAS FROM A RANGE OF HUMAN TISSUES, Genomics, 31(1), 1996, pp. 130-134

Authors: STEVENS HP KELSELL DP BRYANT SP BISHOP DT DAWBER RPR SPURR NK LEIGH IM
Citation: Hp. Stevens et al., LINKAGE OF MONILETHRIX TO THE TRICHOCYTE AND EPITHELIAL KERATIN GENE-CLUSTER ON 12Q11-Q13, Journal of investigative dermatology, 106(4), 1996, pp. 795-797

Authors: STEVENS HP KELSELL DP BRYANT SP BISHOP T SPURR NK WEISSENBACH J MARGER D MARGER RS LEIGH IM
Citation: Hp. Stevens et al., LINKAGE OF AN AMERICAN PEDIGREE WITH PALMOPLANTAR KERATODERMA AND MALIGNANCY (PALMOPLANTAR ECTODERMAL DYSPLASIA TYPE-III) TO 17Q24 - LITERATURE SURVEY AND PROPOSED UPDATED CLASSIFICATION OF THE KERATODERMAS, Archives of dermatology, 132(6), 1996, pp. 640-651

Authors: COX SA ATTWOOD J BRYANT SP BAINS R POVEY R POVEY S REBELLO M KAPSETAKI M MOSCHONAS NK GRZESCHIK KH OTTO M DIXON M SUDWORTH HE KOOY RF WRIGHT A TEAGUE P TERRENATO L VERGNAUD G MONFOUILLOUX S WEISSENBACH J ALIBERT O DIB C FAURE S BAKKER E PEARSON NM VOSSEN RHAM GAL A MUELLERMYHSOK B CANN HM SPURR NK
Citation: Sa. Cox et al., EUROPEAN GENE-MAPPING PROJECT (EUROGEM) - BREAKPOINT PANELS FOR HUMAN-CHROMOSOMES BASED ON THE CEPH REFERENCE FAMILIES, Annals of Human Genetics, 60, 1996, pp. 447-486

Authors: DEWALD G CICHON S BRYANT SP HEMMER S NOTHEN MM SPURR NK
Citation: G. Dewald et al., THE HUMAN-COMPLEMENT C8G GENE, A MEMBER OF THE LIPOCALIN GENE FAMILY - POLYMORPHISMS AND MAPPING TO CHROMOSOME 9Q34.3, Annals of Human Genetics, 60, 1996, pp. 281-291

Authors: BOUZYK M EVANS C CULLIN L COX S WARNE D NYBERG K BRYANT SP SPURR NK
Citation: M. Bouzyk et al., ISOLATION AND MAPPING OF 3 NEW POLYMORPHIC MARKERS TO CHROMOSOME-3, CHROMOSOME-20 AND CHROMOSOME-21, Annals of Human Genetics, 60, 1996, pp. 73-77

Authors: KELSELL DP STEVENS HP RATNAVEL R BRYANT SP BISHOP DT LEIGH IM SPURR NK
Citation: Dp. Kelsell et al., GENETIC-LINKAGE STUDIES IN NON-EPIDERMOLYTIC PALMOPLANTAR KERATODERMA- EVIDENCE FOR HETEROGENEITY, Human molecular genetics, 4(6), 1995, pp. 1021-1025

Authors: STEVENS HP KELSELL DP SHAMSHER M RATNAVEL R NAVSARIA HA SPURR N BISHOP DT BRYANT SP MARGER D MARGER FS GRIFFITHS WAD LEIGH IM
Citation: Hp. Stevens et al., BOWEL EVANS-SYNDROME IS LIKED TO 17Q24 BUT AN IDENTICAL CUTANEOUS PHENOTYPE CAN RESULT FROM K16 MUTATIONS, Journal of investigative dermatology, 105(3), 1995, pp. 456-456

Authors: STEVENS HP KELSELL DP SPURR NK BRYANT SP MARGER D MARGER RS BISHOP DT LEIGH IM
Citation: Hp. Stevens et al., PALMOPLANTAR KERATODERMA (PPK) AND CARCINOMA OF THE ESOPHAGUS - LINKAGE ANALYSIS AND DESCRIPTION OF A UNIQUE PHENOTYPE, Journal of investigative dermatology, 104(4), 1995, pp. 605-605

Authors: DECKERT J NOTHEN MM BRYANT SP REN HZ WOLF HK STILES GL SPURR NK PROPPING P
Citation: J. Deckert et al., HUMAN ADENOSINE A(1) RECEPTOR GENE - SYSTEMATIC SCREENING FOR DNA-SEQUENCE VARIATION AND LINKAGE MAPPING ON CHROMOSOME 1Q31-32.1 USING A SILENT POLYMORPHISM IN THE CODING REGION, Biochemical and biophysical research communications, 214(2), 1995, pp. 614-621

Authors: COX S BRYANT SP COLLINS A WEISSENBACH J DONISKELLER H KOELEMAN BPC STEINKASSERER A SPURR NK
Citation: S. Cox et al., INTEGRATED GENETIC-MAP OF HUMAN-CHROMOSOME-2, Annals of Human Genetics, 59, 1995, pp. 413-434

Authors: SPURR NK KELSELL DP MAVRAKIS E BRYANT SP CROCKFORD G BISHOP DT
Citation: Nk. Spurr et al., GENETIC-HETEROGENEITY IN UK BREAST AND OVARIAN-CANCER FAMILIES, American journal of human genetics, 57(4), 1995, pp. 12-12

Authors: KELSELL DP STEVENS HP BRYANT SP MARGER D MARGER RS LEIGH IM BISHOP DT WEISSENBACH J SPURR NK
Citation: Dp. Kelsell et al., GENETIC-ANALYSIS OF FAMILIES WITH FOCAL PALMOPLANTAR KERATODERMA WITHOR WITHOUT MALIGNANCY, American journal of human genetics, 57(4), 1995, pp. 112-112

Authors: BOUZYK M BRYANT SP SCHMIDT K GOODFELLOW PN SPURR NK
Citation: M. Bouzyk et al., CONSTRUCTION OF A RADIATION HYBRID MAP OF CHROMOSOME 9P, American journal of human genetics, 57(4), 1995, pp. 1490-1490
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