Excavations in the medieval burgh of Aberdeen 1973-81MURRAY, J. C.1982, 255 p., isbn 0-903903-02-4Book

Keloids and hypertrophic scarsMURRAY, J. C.Clinics in dermatology. 1994, Vol 12, Num 1, pp 27-37, issn 0738-081XArticle

Pregnancy and the skinMURRAY, J. C.Dermatologic clinics. 1990, Vol 8, Num 2, pp 327-334, issn 0733-8635, 8 p.Article

Gene/environment causes of cleft lip and/or palateMURRAY, J. C.Clinical genetics. 2002, Vol 61, Num 4, pp 248-256, issn 0009-9163Article

Coagulation and cancerMURRAY, J. C.British journal of cancer. 1991, Vol 64, Num 3, pp 422-424, issn 0007-0920Article

On the boundary-value problem associated with a general twisted tube with a slowly varying circular sectionMURRAY, J. C.Quarterly of applied mathematics. 1984, Vol 42, Num 3, pp 257-265, issn 0033-569XArticle

Scars and keloids : Wound healingMURRAY, J. C.Dermatologic clinics. 1993, Vol 11, Num 4, pp 697-708, issn 0733-8635Article

Pyoderma gangrenosum with IgA gammopathyMURRAY, J. C.Cutis (New York, NY). 1983, Vol 32, Num 5, pp 477-486, issn 0011-4162Article

The Scottish Burgh Survey - a reviewMURRAY, J. C.Proceedings of the Society of the Antiquaries of Scotland. 1983, Vol 113, pp 1-10Article

Clinical findings in patients with GLI2 mutations ― phenotypic variabilityBERTOLACINI, Cdp; RIBEIRO-BICUDO, L. A; PETRIN, A et al.Clinical genetics. 2012, Vol 81, Num 1, pp 70-75, issn 0009-9163, 6 p.Article

Mutations in PITX2 may contribute to cases of omphalocele and VATER-like syndromesKATZ, L. A; SCHULTZ, R. E; SEMINA, E. V et al.American journal of medical genetics. 2004, Vol 130A, Num 3, pp 277-283, issn 0148-7299, 7 p.Article

Endothelial cells as therapeutic targets in cancer: New biology and novel delivery systemsMURRAY, J. C; MOGHIMI, S. M.Critical reviews in therapeutic drug carrier systems. 2003, Vol 20, Num 2-3, pp 139-152, issn 0743-4863, 14 p.Article

Two novel frameshift mutations in NKX2.5 result in novel features including visceral inversus and sinus venosus type ASDWATANABE, Y; BENSON, D. W; YANO, S et al.Journal of medical genetics. 2002, Vol 39, Num 11, pp 807-811, issn 0022-2593, 5 p.Article

Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palateYOSHIURA, K.-I; MACHIDA, J; DAACK-HIRSCH, S et al.Genomics (San Diego, Calif.). 1998, Vol 54, Num 2, pp 231-240, issn 0888-7543Article

Isochromosome 7q in childhood myelodysplastic syndromeMURRAY, J. C; MAHONEY, D. H; COOLEY, L. D et al.Leukemia. 1996, Vol 10, Num 4, pp 746-747, issn 0887-6924Article

Lymphoblastic lymphoma following prenatal exposure to phenytoinMURRAY, J. C; HILL, R. M; HEGEMIER, S et al.Journal of pediatric hematology/oncology. 1996, Vol 18, Num 2, pp 241-243, issn 1077-4114Article

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndromeSEMINA, E. V; REITER, R; CAREY, J. C et al.Nature genetics. 1996, Vol 14, Num 4, pp 392-399, issn 1061-4036Article

Changes in cartilage composition and physical properties due to stromelysin degradationBONASSAR, L. J; FRANK, E. H; MURRAY, J. C et al.Arthritis and rheumatism. 1995, Vol 38, Num 2, pp 173-183, issn 0004-3591Article

Cutaneous infection caused by Curvularia pallescens : a case report and review of the spectrum of diseaseBERG, D; GARCIA, J. A; SCHELL, W. A et al.Journal of the American Academy of Dermatology. 1995, Vol 32, Num 2, pp 375-378, issn 0190-9622, 2Article

Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease)MURRAY, J. C; ROSSMANN, S. N; MURALI CHINTAGUMPALA et al.Archives of pediatrics & adolescent medicine. 1995, Vol 149, Num 1, pp 57-58, issn 1072-4710Article

Isolation of yeast artificial chromosome clones from 54 polymorphic loci mapped with high odds on human chromosome 4JIAN-BING FAN; DEYOUNG, J; MYERS, R. M et al.Human molecular genetics (Print). 1994, Vol 3, Num 2, pp 243-246, issn 0964-6906Article

Keloids treated with excision followed by radiation therapyKLUMPAR, D. I; MURRAY, J. C; ANSCHER, M et al.Journal of the American Academy of Dermatology. 1994, Vol 31, Num 2, pp 225-231, issn 0190-9622, 1Article

Prolongation of the prothrombin time after organophosphate poisoningMURRAY, J. C; STEIN, F; MCGLOTHLIN, J. C et al.Pediatric emergency care. 1994, Vol 10, Num 5, pp 289-290, issn 0749-5161Conference Paper

Acquired cutaneous smooth muscle hamartomaDARLING, T. N; KAMINO, H; MURRAY, J. C et al.Journal of the American Academy of Dermatology. 1993, Vol 28, Num 5, pp 844-845, issn 0190-9622, 2Article

The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the fascioscapulohumeral muscular dystrophy locusWIJMENGA, C; WINOKUR, S. T; PADBERG, G. W et al.Human genetics. 1993, Vol 92, Num 2, pp 198-203, issn 0340-6717Article