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Journal of Laparoendoscopic Surgery|February 1, 1993
Routine or selective intraoperative cholangiography in laparoscopic cholecystectomyM A Carlson, K A Ludwig, C T Frantzides, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
A 6p22 reference map of leukocyte DNA: exclusion of rearrangement in four cases of atypical haemochromatosisD F Wallace, J Partridge, A Robertson, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|July 1, 1990
The international validation of a fixed-dose procedure as an alternative to the classical LD50 testM J van den Heuvel, D G Clark, R J Fielder, et al.
American Journal of Human Genetics|June 1, 1996
Mutations and phenotype in isolated glycerol kinase deficiencyA P Walker, F Muscatelli, A N Stafford, et al.
Clinical Nuclear Medicine|June 1, 1992
Imaging of regional spread of breast cancer by internal mammary lymphoscintigraphy, CT, and MRIH T Turoglu, N A Janjan, M K Thorsen, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|March 1, 1995
Comparison of the up-and-down, conventional LD50, and fixed-dose acute toxicity proceduresR L Lipnick, J A Cotruvo, R N Hill, et al.
Human Molecular Genetics|November 1, 1992
A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genesA P Walker, J Chelly, D R Love, et al.
Human Molecular Genetics|April 1, 1992
Reconstruction of the 2.4 Mb human DMD-gene by homologous YAC recombinationJ T Den Dunnen, P M Grootscholten, J G Dauwerse, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|September 29, 2012
Genetic analysis of NR0B1 in congenital adrenal hypoplasia patients: identification of a rare regulatory variant resulting in congenital adrenal hypoplasia and hypogonadal hypogonadism without testicular carcinoma in situA P Walker, R C Fowkes, F Saleh, et al.
Prenatal Diagnosis|January 1, 1991
Identification of Duchenne muscular dystrophy genomic probe P20 constant Taql fragment corresponding to the EcoRV and Mspl polymorphismsN G Laing, A P Walker, P A Akkari, et al.
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