Authors:
Gozukara, EM
Khan, SG
Metin, A
Emmert, S
Busch, DB
Shahlavi, T
Coleman, DM
Miller, M
Chinsomboon, N
Stefanini, M
Kraemer, KH
Citation: Em. Gozukara et al., A stop codon in xeroderma pigmentosum group C families in Turkey and Italy: Molecular genetic evidence for a common ancestor, J INVES DER, 117(2), 2001, pp. 197-204
Authors:
Kilic, SS
Tezcan, I
Sanal, O
Metin, A
Ersoy, F
Citation: Ss. Kilic et al., Transient hypogammaglobulinemia of infancy: Clinical and immunologic features of 40 new cases, PEDIATR INT, 42(6), 2000, pp. 647-650
Authors:
Sanal, O
Yel, L
Kucukali, T
Gilbert-Barnes, E
Tardieu, M
Tezcan, I
Ersoy, F
Metin, A
de Saint Basile, G
Citation: O. Sanal et al., An allelic variant of Griscelli disease: presentation with severe hypotonia, mental-motor retardation, and hypopigmentation consistent with Elejalde syndrome (neuroectodermal melanolysosomal disorder), J NEUROL, 247(7), 2000, pp. 570-572
Authors:
Sanal, O
Ersoy, F
Yel, L
Tezcan, I
Metin, A
Ozyurek, H
Gariboglu, S
Fikrig, S
Berkel, AI
Rijkers, GT
Zegers, BJM
Citation: O. Sanal et al., Impaired IgG antibody production to pneumococcal polysaccharides in patients with ataxia-telangiectasia, J CLIN IMM, 19(5), 1999, pp. 326-334
Authors:
Tezcan, I
Sanal, O
Ersoy, F
Uckan, D
Kilic, S
Metin, A
Cetin, M
Akun, R
Oner, C
Tuncer, AM
Citation: I. Tezcan et al., Successful bone marrow transplantation in a case of Griscelli disease which presented in accelerated phase with neurological involvement, BONE MAR TR, 24(8), 1999, pp. 931-933