T. V. Zolotukhina

Amniotic fluid cell culture for prenatal diagnosis of some metabolic diseases

T. V. Zolotukhina, I. Tsvetkova, 1980, Bulletin of Experimental Biology and Medicine.

Analysis of Cell-free Fetal DNA in Plasma and Serum of Pregnant Women

T. V. Zolotukhina, N. V. Shilova, E. Voskoboeva, 2005, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Ovotesticular disorder of sexual development due to gonosomal mosaicism

T. V. Zolotukhina, N. Shilova, V. Chernykh, 2010 .

Hidden X Chromosomal Mosaicism in a 46,XX Male

A. Polyakov, T. V. Zolotukhina, N. Shilova, 2009, Sexual Development.

Geneticl and clinical characteristics of 22q11.2 deletion syndrome

I. Kazantseva, A. Polyakov, T. V. Zolotukhina, 2014, Russian Journal of Genetics.

Use of 4-trifluoromethylumbelliferyl-alpha-L-iduronide as a new substrate for detection of alpha-L-iduronidase deficiency in human tissues and for rapid prenatal diagnosis of Hurler disease.

V. Biryukov, T. V. Zolotukhina, E. Karpova, 1991, Journal of inherited metabolic disease.

Range of the rare chromosomal abnormalities diagnosed prenatally at fetuses with increased nuchal translucency

T. V. Zolotukhina, N. Shilova, Zhanna G. Markova, 2013 .

Use of 4-trifluoromethylumbelliferyl-α-l-iduronide as a new substrate for detection of α-l-iduronidase deficiency in human tissues and for rapid prenatal diagnosis of Hurler disease

V. Biryukov, T. V. Zolotukhina, E. Karpova, 1991, Journal of Inherited Metabolic Disease.

Generation and application of dynamic standard reference intervals for analyzing results of comparative genomic hybridization

I. Lebedev, V. Zemlyakova, T. V. Zolotukhina, 2013, Russian Journal of Genetics.