Molecular analysis of patients with aniridia in Russian Federation broadens the spectrum of PAX6 mutations von Vasilyeva, T.A., Voskresenskaya, A.A., Käsmann‐Kellner, B., Khlebnikova, O.V., Pozdeyeva, N.A., Bayazutdinova, G.M., Kutsev, S.I., Ginter, E.K., Semina, E.V., Marakhonov, A.V., Zinchenko, R.A.

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Genetic relationships of Asians and Northern Europeans, revealed by Y-chromosomal DNA analysis von Zerjal, T, Dashnyam, B, Pandya, A, Kayser, M, Roewer, L, Santos, F R, Schiefenhövel, W, Fretwell, N, Jobling, M A, Harihara, S, Shimizu, K, Semjidmaa, D, Sajantila, A, Salo, P, Crawford, M H, Ginter, E K, Evgrafov, O V, Tyler-Smith, C

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Laminopathies in Russian families von Rudenskaya, GE, Polyakov, AV, Tverskaya, SM, Zaklyazminskaya, EV, Chukhrova, AL, Groznova, OE, Ginter, EK

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Linkage of Polymorphic Congenital Cataract to the γ-Crystallin Gene Locus on Human Chromosome 2q33–35 von Rogaev, Evgeny I., Rogaeva, Ekaterina A., Korovaitseva, Galina I., Farrer, Lindsay A., Petrin, Alexander N., Keryanov, Sergey A., Turaeva, Shirine, Chumakov, Ilya, George-Hyslop, Peter St, Ginter, Eugeny K.

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Spectrum of mutations in BRCA1 gene in hereditary forms of breast and ovarian cancer in Russian families von Loginova, A N, Pospekhova, N I, Lyubchenko, L N, Budilov, A V, Zakhar'ev, V M, Gar'kavtseva, R F, Ginter, E K, Karpukhin, A V

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Haemophilia: strategies for carrier detection and prenatal diagnosis von PEAKE, I. R, LILLICRAP, D. P, TUDDENHAM, E. G. D, BOULYJENKOV, V, BRIET, E, CHAN, V, GINTER, E. K, KRAUS, E. M, LJUNG, R, MANNUCCI, P. M, NICOLAIDES, K

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Total hypotrichosis: genetic form of alopecia not linked to hairless gene von Rogaev, EI, Zinchenko, RA, Dvoryachikov, G, Sherbatich, T, Ginter, EK

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Report of a joint WHO/WFH meeting on the control of haemophilia: carrier detection and prenatal diagnosis von Peake, I R, Lillicrap, D P, Boulyjenkov, V, Briët, E, Chan, V, Ginter, E K, Kraus, E M, Ljung, R, Mannucci, P M, Nicolaides, K, Tuddenham, E G. D

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Integrated Population Genetic and Medical Genetic Study of Two Raions of the Tver Oblast von Frisman, E. Ya, Zhdanova, O. L.

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New mutations in the APC gene in familial adenomatous polyposis: detection, characterization, and analysis von Muzaffarova, T A, Pospekhova, N I, Sachkov, I Yu, Kuz'minov, A M, Ginter, E K, Karpukhin, A V

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Genetic Services in Russia von Baranov, V.S., Ginter, E.K.

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Identification of the genetic locus for keratosis palmaris et plantaris on chromosome 17 near the RARA and keratin type I genes von Rogaev, Evgeny I, Rogaeva, Ekaterina A, Ginter, Eugene K, Korovaitseva, Galina I, Farrer, Lindsay A, Shlensky, Alexander B, Pritkov, Alexander N, Mordovtsev, Vladimir N, St George-Hyslop, Peter H

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Population-Genetic Structure of Chuvash Populations Inferred from the Data on Eight DNA Loci of the Nuclear Genome von Khusnutdinova, E. K., Victorova, T. V., Akhmetova, V. L., Mustafina, O. E., Fatkhlislamova, R. I., Balanovskaya, E. V., Petrova, N. V., Makarov, S. V., Kravchuk, O. I., Pai, G. V., Ginter, E. K.

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Effect of the degree of differentiation on growth of anlagen of the long bones of the limb in mouse embryos in vitro von Ginter, E. K.

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Emery-Dreifuss syndrome: Genetic and clinical varieties von Rudenskaya, G. E., Ginter, E. K., Petrin, A. N., Djomina, N. A.

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Action of triiodothyronine on in vitro growth of anlagen of mouse limb bones in a mutant of lines brachypodism-H and C57Bl, 61 von Ginter, E. K., Konyukhov, B. V.

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