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KH C
SKOBELEVA NA
SHEVTSOV SP
KONSTANTINOV VO
DENISENKO AD
SCHWARTZ EI
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Authors:
CHAKIR K
SKOBELEVA NA
SHEVTSOV SP
KONSTANTINOV VO
DENISENKO AD
SCHWARTZ E
Citation: K. Chakir et al., A NOVEL E397X MUTATION IN THE LDL RECEPTOR GENE IN FH PATIENTS FROM ST-PETERSBURG, RUSSIA, European journal of human genetics, 6, 1998, pp. 4065-4065
Citation: Sp. Shevtsov, THE APO-B GENE ENCODING PUTATIVE LOW-DENS ITY-LIPOPROTEIN RECEPTOR-BINDING DOMAIN OF THE APO-B-100 PROTEIN SHOWS NO DNA POLYMORPHISMS, Genetika, 32(2), 1996, pp. 295-297
Authors:
BARANOVSKAYA SS
SHEVTSOV SP
MAKSIMOVA SP
KUZMIN AI
SCHWARTZ EI
Citation: Ss. Baranovskaya et al., SPECTRUM OF PHENYLKETONURIA MUTATIONS OF PHENYLALANIN HYDROXYLASE GENE IN ST-PETERSBURG POPULATION, Doklady Akademii nauk. Rossijskaa akademia nauk, 340(5), 1995, pp. 709-711
Authors:
PUSHNOVA EA
AKHMEDOVA SN
SHEVTSOV SP
SCHWARTZ EI
Citation: Ea. Pushnova et al., A RAPID AND SIMPLE DNA-FINGERPRINTING METHOD USING RLFP AND SSCP ANALYSIS OF THE HYPERVARIABLE NONCODING REGION OF HUMAN MITOCHONDRIAL-DNA, Human mutation, 3(3), 1994, pp. 292-296
Authors:
SHEVTSOV SP
RECHITSKY S
VERLINSKY O
SCHWARTZ EI
Citation: Sp. Shevtsov et al., NONISOTOPIC IDENTIFICATION OF 2 POINT MUTATIONS IN THE CYP21 GENE RESPONSIBLE FOR NONCLASSIC 21-HYDROXYLASE DEFICIENCY, Biochemical medicine and metabolic biology, 52(2), 1994, pp. 85-88