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Results:
1-8
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Results: 8
Authors:
Jakubiczka, S
Bettecken, T
Koch, G
Tuysuz, B
Wollnik, B
Wieacker, P
Citation: S. Jakubiczka et al., Campomelic dysplasia without sex reversal in a Turkish patient is due to mutation Ala119Val within the SOX9 gene, CLIN DYSMOR, 10(3), 2001, pp. 197-201
Authors:
Tuysuz, B
Beker, BD
Centel, T
Ungur, S
Iter, O
Citation: B. Tuysuz et al., Unilateral tibial agenesia with preaxial polysyndactyly and renal disorderin two patients: a new syndrome?, CLIN DYSMOR, 10(1), 2001, pp. 37-40
Authors:
Bomont, P
Cavalier, L
Blondeau, F
Hamida, CB
Belal, S
Tazir, M
Demir, E
Topaloglu, H
Korinthenberg, R
Tuysuz, B
Landrieu, P
Hentati, F
Koenig, M
Citation: P. Bomont et al., The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy, NAT GENET, 26(3), 2000, pp. 370-374
Authors:
Afzal, AR
Rajab, A
Fenske, CD
Oldridge, M
Elanko, N
Ternes-Pereira, E
Tuysuz, B
Murday, VA
Patton, MA
Wilkie, AOM
Jeffery, S
Citation: Ar. Afzal et al., Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2, NAT GENET, 25(4), 2000, pp. 419-422
Authors:
Tuysuz, B
Hacihanefioglu, S
Silahtaroglu, A
Yilmaz, S
Deviren, A
Cenani, A
Citation: B. Tuysuz et al., Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation, GEN COUNSEL, 11(4), 2000, pp. 355-361
Authors:
Tuysuz, B
Ungur, S
Akalin, F
Cenani, A
Tunnessen, WW
Citation: B. Tuysuz et al., Picture of the month - Keutel syndrome, ARCH PED AD, 153(7), 1999, pp. 765-766
Authors:
Tuysuz, B
Mercimek, S
Ungur, S
Deniz, M
Citation: B. Tuysuz et al., Calcitonin treatment in osteoectasia with hyperphosphatasia (juvenile Paget's disease): radiographic changes after treatment, PEDIAT RAD, 29(11), 1999, pp. 838-841
Authors:
Erkan, T
Kutlu, T
Cullu, F
Celik, M
Demir, T
Tuysuz, B
Tumay, GT
Citation: T. Erkan et al., Hennekam syndrome, ARCH PED, 5(12), 1998, pp. 1344-1346
Risultati:
1-8
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