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Results:
1-9
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Results: 9
Authors:
Oktenli, C
Ulucan, H
Saglam, M
Gul, D
Citation: C. Oktenli et al., Camptodactyly, skeletal changes, ptosis and infertility in a male: a new syndrome?, CLIN DYSMOR, 10(4), 2001, pp. 295-297
Authors:
Unay, B
Sarici, SU
Gul, D
Akin, R
Gokcay, E
Citation: B. Unay et al., Adams-Oliver syndrome: further evidence for autosomal recessive inheritance, CLIN DYSMOR, 10(3), 2001, pp. 223-225
Authors:
Caglayan, S
Ozata, M
Ozisik, G
Turan, M
Bolu, E
Oktenli, C
Arslan, N
Erbil, K
Gul, D
Ozdemir, IC
Citation: S. Caglayan et al., Plasma melatonin concentration before and during testosterone replacement in Klinefelter's syndrome: Relation to hepatic indolamine metabolism and sympathoadrenal activity, J CLIN END, 86(2), 2001, pp. 738-743
Authors:
Gul, D
Odabas, E
Kutlu, M
Citation: D. Gul et al., Oculocutaneous albinism and reduced bone density in two sibs: a new autosomal recessive syndrome?, CLIN DYSMOR, 9(4), 2000, pp. 295-296
Authors:
Gul, D
Ozata, M
Mergen, H
Odabasi, Z
Mergen, M
Citation: D. Gul et al., Woodhouse and Sakati syndrome (MIM 241080). report of a new patient, CLIN DYSMOR, 9(2), 2000, pp. 123-125
Authors:
Gul, D
Ozturk, H
Citation: D. Gul et H. Ozturk, Unilateral proximal femoral focal deficiency and Hirschsprung disease, CLIN DYSMOR, 9(2), 2000, pp. 149-150
Authors:
Gul, D
Oktenli, C
Saglam, M
Erdem, U
Citation: D. Gul et al., Craniofacial anomalies, ocular findings, pigmented nevi, camptodactyly, and skeletal changes: a possible new autosomal recessive disorder, CLIN DYSMOR, 9(1), 2000, pp. 61-62
Authors:
Alpay, F
Gul, D
Lenk, MK
Ogur, G
Citation: F. Alpay et al., Severe intrauterine growth retardation, aged facial appearance, and congenital heart disease in a newborn with Johanson-Blizzard syndrome, PEDIAT CARD, 21(4), 2000, pp. 389-390
Authors:
Ilker, SS
Ozturk, F
Kurt, E
Temel, M
Gul, D
Sayli, BS
Citation: Ss. Ilker et al., Ophthalmic findings in GAPO syndrome, JPN J OPHTH, 43(1), 1999, pp. 48-52
Risultati:
1-9
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