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Results:
1-7
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Results: 7
Authors:
BRADSHAW N
BREWER C
FITZPATRICK D
MURRAY G
RODGERS F
PORTEOUS M
CAMPBELL H
Citation: N. Bradshaw et al., GUIDELINES AND CARE PATHWAYS FOR GENETIC-DISEASES - THE SCOTTISH COLLABORATIVE PROJECT ON TUBEROUS SCLEROSIS, European journal of human genetics, 6(5), 1998, pp. 445-458
Authors:
CAMPBELL H
HOTCHKISS R
BRADSHAW N
PORTEOUS M
Citation: H. Campbell et al., INTEGRATED CARE PATHWAYS, BMJ. British medical journal, 316(7125), 1998, pp. 133-137
Authors:
BECHER MW
RUBINSZTEIN DC
LEGGO J
WAGSTER MV
STINE OC
RANEN NG
FRANZ ML
ABBOTT MH
SHERR M
MACMILLAN JC
BARRON L
PORTEOUS M
HARPER PS
ROSS CA
Citation: Mw. Becher et al., DENTATORUBRAL AND PALLIDOLUYSIAN ATROPHY (DRPLA) - CLINICAL AND NEUROPATHOLOGICAL FINDINGS IN GENETICALLY CONFIRMED NORTH-AMERICAN AND EUROPEAN PEDIGREES, Movement disorders, 12(4), 1997, pp. 519-530
Authors:
CAMPBELL H
MACKAY J
PORTEOUS M
Citation: H. Campbell et al., THE FUTURE OF BREAST AND OVARIAN-CANCER CLINICS - NO LONGER JUST RESEARCH - NOW A CLINICAL NEED, BMJ. British medical journal, 311(7020), 1995, pp. 1584-1585
Authors:
PASTERIS NG
CADLE A
LOGIE LJ
PORTEOUS M
SCHWARTZ CE
STEVENSON RE
GLOVER TW
WILROY RS
GORSKI JL
Citation: Ng. Pasteris et al., ISOLATION AND ANALYSIS OF THE FACIOGENITAL DYSPLASIA (AARSKOG-SCOTT SYNDROME) GENE - A PUTATIVE RHO RAC GUANINE-NUCLEOTIDE EXCHANGE FACTOR/, American journal of human genetics, 55(3), 1994, pp. 10000003-10000003
Authors:
NORTON B
LANYON WG
MOORE MR
PORTEOUS M
YOUNGS GR
CONNOR JM
Citation: B. Norton et al., EVIDENCE FOR INVOLVEMENT OF A 2ND GENETIC-LOCUS ON CHROMOSOME-11Q IN PORPHYRIN METABOLISM, Human genetics, 91(6), 1993, pp. 576-578
Authors:
BARRON LH
WARNER JP
PORTEOUS M
HOLLOWAY S
SIMPSON S
DAVIDSON R
BROCK DJH
Citation: Lh. Barron et al., A STUDY OF THE HUNTINGTONS-DISEASE ASSOCIATED TRINUCLEOTIDE REPEAT INTHE SCOTTISH POPULATION, Journal of Medical Genetics, 30(12), 1993, pp. 1003-1007
Risultati:
1-7
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