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au.\*:("SAMUELS, M. E")

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A rural-urban comparative study of nonphysician providers in community and migrant health centersSHI, L; SAMUELS, M. E; RICKETTS, T. C et al.Public health reports (1974). 1994, Vol 109, Num 6, pp 809-815, issn 0033-3549Article

Identification of a common variant in the lipoprotein lipase gene in a large Utah kindred ascertained for coronary heart disease : the - 93G/D9N variant predisposes to low HDL-C/high triglyceridesSAMUELS, M. E; FORBEY, K. C; SKOLNICK, M. H et al.Clinical genetics. 2001, Vol 59, Num 2, pp 88-98, issn 0009-9163Article

Patient characteristics associated with hospitalizations for ambulatory care sensitive conditions in South CarolinaLEIYU SHI; SAMUELS, M. E; PEASE, M et al.Southern medical journal (Birmingham). 1999, Vol 92, Num 10, pp 989-998, issn 0038-4348Conference Paper

46, XY gonadal dysgenesis: new SRY point mutation in two siblings with paternal germ line mosaicismSTOPPA-VAUCHER, S; AYABE, T; PAQUETTE, J et al.Clinical genetics. 2012, Vol 82, Num 6, pp 505-513, issn 0009-9163, 9 p.Article

A homozygous HAMP mutation in a multiply consanguineous family with pseudo-dominant juvenile hemochromatosisDELATYCKI, M. B; ALLEN, K. J; GOW, P et al.Clinical genetics. 2004, Vol 65, Num 5, pp 378-383, issn 0009-9163, 6 p.Article

The complex set of late transcripts from the Drosophila sex determination gene sex-lethal encodes multiple related polypeptidesSAMUELS, M. E; SCHEDL, P; CLINE, T. W et al.Molecular and cellular biology (Print). 1991, Vol 11, Num 7, pp 3584-3602, issn 0270-7306Article

The Drosophila female-specific sex-determination gene, Sex-lethal, has stage-, tissue-, and sex-specific RNAs suggesting multiple modes of regulationSALZ, H. K; MAINE, E. M; KEYES, L. N et al.Genes & development. 1989, Vol 3, Num 5, pp 708-719, issn 0890-9369Article

Novel mutations in the sacsin gene in ataxia patients from Maritime CanadaGUERNSEY, D. L; DUBE, M.-P; RIDEOUT, A et al.Journal of the neurological sciences. 2010, Vol 288, Num 1-2, pp 79-87, issn 0022-510X, 9 p.Article

Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populationsGOLDBERG, Y. P; MACFARLANE, J; PAYNE, B et al.Clinical genetics. 2007, Vol 71, Num 4, pp 311-319, issn 0009-9163, 9 p.Article

Genetic localization to chromosome 1p32 of the third locus for familial hypercholesterolemia in a Utah kindredHUNT, S. C; HOPKINS, P. N; BULKA, K et al.Arteriosclerosis, thrombosis, and vascular biology. 2000, Vol 20, Num 4, pp 1089-1093, issn 1079-5642Article

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