The Forensic Science Service : What Is Its Impact?RAMSAY, M.Research Bulletin. 1986, Num 22, pp 18-20Article

THE IMPROVING OUTLOOK FOR THE SMALL PREMATURELY BORN INFANTFITZHARDINGE PM; RAMSAY M.1973; DEVELOP. MED. CHILD NEUROL.; G.B.; DA. 1973; VOL. 15; NO 4; PP. 447-459; ABS. FR. ALLEM. ESP.; BIBL. 19REF.Serial Issue

Yeast artificial chromosome cloningRAMSAY, M.Molecular biotechnology. 1994, Vol 1, Num 2, pp 181-201, issn 1073-6085Article

Housing for the Homeless Ex-Offender : Key Findings from a Literature ReviewRAMSAY, M.Research Bulletin. 1986, Num 20, pp 57-60Article

A COMPARISON OF TWO DEVELOPMENTAL SCALES IN EVALUATING INFANTS WITH DOWN SYNDROMERAMSAY M; PIPER MC.1980; EARLY HUM. DEVELOP.; NLD; DA. 1980; VOL. 4; NO 1; PP. 89-95; BIBL. 14 REF.Article

A COMPARATIVE STUDY OF TWO DEVELOPMENTAL SCALES. THE BAYLEY AND THE GRIFFITHS.RAMSAY M; FITZHARDINGE PM.1977; EARLY HUM. DEVELOP.; NETHERL.; DA. 1977; VOL. 1; NO 2; PP. 151-157; BIBL. 24 REF.Article

La Commission canadienne des droits de la personne et l'équité en matière d'emploiFALARDEAU-RAMSAY, M.Revue Juridique et Politique. Indépendance et Coopération. 1989, Num 3-4, pp 665-675Article

A measles outbreak in the Irish traveller ethnic group after attending a funeral in England, March-June 2007COHUET, S; BUKASA, A; HEATHCOCK, R et al.Epidemiology and infection. 2009, Vol 137, Num 12, pp 1759-1765, issn 0950-2688, 7 p.Article

Clinical and molecular characterization of lipoid proteinosis in Namaqualand, South AfricaVAN HOUGENHOUCK-TULLEKEN, W; CHAN, I; HAMADA, T et al.British journal of dermatology (1951). 2004, Vol 151, Num 2, pp 413-423, issn 0007-0963, 11 p.Article

First report of CFTR mutations in black cystic fibrosis patients of southern African originCARLES, S; DESGEORGES, M; GOLDMAN, A et al.Journal of medical genetics. 1996, Vol 33, Num 9, pp 802-804, issn 0022-2593Article

New founder haplotypes at the myotonic dystrophy locus in Southern AfricaGOLDMAN, A; RAMSAY, M; JENKINS, T et al.American journal of human genetics. 1995, Vol 56, Num 6, pp 1373-1378, issn 0002-9297Article

Molecular analysis of the CTG trinucleotide repeat in South African myotonic dystrophy families : implications for diagnosis and counsellingGOLDMAN, A; RAMSAY, M; JENKINS, T et al.SAMJ. South African medical journal. 1995, Vol 85, Num 11, pp 1161-1164, issn 0256-9574Article

Distinct components of spatial learning revealed by prior training and NMDA receptor blockadeBANNERMAN, D. M; GOOD, M. A; BUTCHER, S. P et al.Nature (London). 1995, Vol 378, Num 6553, pp 182-186, issn 0028-0836Article

Absence of myotonic dystrophy in southern African Negroids is associated with a significantly lower number of CTG trinucleotide repeatsGOLDMAN, A; RAMSAY, M; JENKINS, T et al.Journal of medical genetics. 1994, Vol 31, Num 1, pp 37-40, issn 0022-2593Article

The high frequency of the Hb B₂ variant in the Herebo population: a founder effect?SPURDLE, A. B; KRAUSE, A; RAMSAY, M et al.Hemoglobin. 1994, Vol 18, Num 4-5, pp 317-323, issn 0363-0269Article

A new negroid-specific HindIII polymorphism in the serum amyloid A1 (SAA1) gene increases the usefulness of the SAA locus in linkage studiesSTEVENS, G; RAMSAY, M; KLUVE-BECKERMAN, B et al.Genomics (San Diego, Calif.). 1993, Vol 15, Num 1, pp 242-243, issn 0888-7543Article

Exclusion of two candidate pigment loci, c and b, part of chromosome 11p, and 33 random polymorphic markers as the locus for tyrosinase-positive oculocutaneous albinismCOLMAN, M. A; STEVENS, G; RAMSAY, M et al.Human genetics. 1993, Vol 90, Num 5, pp 556-560, issn 0340-6717Article

Cystic fibrosis. II: New developments in cystic fibrosis : implications for carrier detection and genetic counsellingDENTER, M; RAMSAY, M; JENKINS, T et al.SAMJ. South African medical journal. 1992, Vol 82, Num 1, pp 11-13, issn 0256-9574Article

A two alleleXbal RFLP at the catalase 2 locusCOLMAN, M.-A; SHIBAHARA, S; KWON, B et al.Nucleic acids research. 1991, Vol 19, Num 4, issn 0305-1048, p. 960Article

A totally failing liver may be more harmful than no liver at all : three cases of total hepatic devascularization in preparation for emergency liver transplantationHUSBERG, B. S; GOLDSTEIN, R. M; KLINTMALM, G. B et al.Transplantation proceedings. 1991, Vol 23, Num 1, pp 1533-1535, issn 0041-1345, 2Conference Paper

First trimester prenatal diagnosis by chorionic villus sampling: the Johannesburg experience with 48 casesROSENDORFF, J; JACOBSON, M. J; MORRIS, D et al.SAMJ. South African medical journal. 1989, Vol 75, Num 1, pp 15-17, issn 0256-9574Article

Mutations for the autosomal recessive and autosomal dominant forms of polycystic kidney disease are not allelicRAMSAY, M; REEDERS, S. T; THOMSON, P. D et al.Human genetics. 1988, Vol 79, Num 1, pp 73-75, issn 0340-6717Article

The haematological puzzle of Hb J cape Town is partly solvedLAMBRIDIS, A. J; RAMSAY, M; JENKINS, T et al.British journal of haematology. 1986, Vol 63, Num 2, pp 363-367, issn 0007-1048Article

Host and environmental factors associated with Hib in England, 1998-2002MCVERNON, J; ANDREWS, N; SLACK, M et al.Archives of disease in childhood. 2008, Vol 93, Num 8, pp 670-675, issn 0003-9888, 6 p.Article

The molecular basis of cystic fibrosis in South AfricaGOLDMAN, A; LABRUM, R; CLAUSTRES, M et al.Clinical genetics. 2001, Vol 59, Num 1, pp 37-41, issn 0009-9163Article