المؤلفون: Wynford-Thomas, D, Parry, EM, Wyllie, FS, Ulucan, H, Parry, JM

المساهمون: 728620

مصطلحات موضوعية: Yaşam Bilimleri (LIFE), Tıp, Sağlık Bilimleri, Dahili Tıp Bilimleri, Tıbbi Genetik, Yaşam Bilimleri, Moleküler Biyoloji ve Genetik, Sitogenetik, Temel Bilimler, BİYOKİMYA VE MOLEKÜLER BİYOLOJİ, GENETİK VE HAYAT

العلاقة: CHROMOSOMA; Parry E., Ulucan H., Wyllie F., Wynford-Thomas D., Parry J., "Segregational fidelity of chromosomes in human thyroid tumour cells", CHROMOSOMA, cilt.107, ss.491-497, 1998; vv_1032021; av_de7ec1c9-3de8-4501-835f-e1b08d31048f; http://hdl.handle.net/20.500.12627/146596Test; https://doi.org/10.1007/s004120050334Test; http://www.ncbi.nlm.nih.gov/pubmed/9914382Test; 107; 491; 497

الإتاحة: https://doi.org/20.500.12627/146596Test
https://doi.org/10.1007/s004120050334Test
https://hdl.handle.net/20.500.12627/146596Test
http://www.ncbi.nlm.nih.gov/pubmed/9914382Test

المؤلفون: Ulucan, H, Gul, D, Unay, B, Akin, R, Gokcay, E

المساهمون: 728654

مصطلحات موضوعية: Sağlık Bilimleri, Dahili Tıp Bilimleri, Tıbbi Genetik, Yaşam Bilimleri, Moleküler Biyoloji ve Genetik, Temel Bilimler, Yaşam Bilimleri (LIFE), Tıp, GENETİK VE HAYAT

العلاقة: CLINICAL DYSMORPHOLOGY; Gul D., Ulucan H., Unay B., Akin R., Gokcay E., "Acrocallosal syndrome: report of five Turkish patients", CLINICAL DYSMORPHOLOGY, cilt.13, ss.241-246, 2004; av_e2c9f6ab-d1d1-49e5-bf55-e100fa3d4bb4; vv_1032021; http://hdl.handle.net/20.500.12627/149271Test; http://www.ncbi.nlm.nih.gov/pubmed/15365461Test; https://doi.org/10.1097/00019605-200410000-00008Test; 13; 241; 246

الإتاحة: https://doi.org/20.500.12627/149271Test
https://doi.org/10.1097/00019605-200410000-00008Test
https://hdl.handle.net/20.500.12627/149271Test
http://www.ncbi.nlm.nih.gov/pubmed/15365461Test

المؤلفون: Saglam, M, Ulucan, H, Gul, D, Oktenli, C

المساهمون: 727244

مصطلحات موضوعية: Temel Bilimler, Dahili Tıp Bilimleri, Moleküler Biyoloji ve Genetik, Tıbbi Genetik, Yaşam Bilimleri, Sağlık Bilimleri, Yaşam Bilimleri (LIFE), Tıp, GENETİK VE HAYAT

العلاقة: CLINICAL DYSMORPHOLOGY; Oktenli C., Ulucan H., Saglam M., Gul D., "Facial dysmorphism, multiple pigmented nevi, osteoporosis, brachydactyly, and other skeletal changes in a male: a new syndrome?", CLINICAL DYSMORPHOLOGY, cilt.12, sa.2, ss.149-151, 2003; vv_1032021; av_2334aee0-92dd-46f5-971d-f6abc0ba27cb; http://hdl.handle.net/20.500.12627/28643Test; http://www.ncbi.nlm.nih.gov/pubmed/12868484Test; https://doi.org/10.1097/01.mcd.0000052340.43310.a7Test; 12; 149; 151

الإتاحة: https://doi.org/20.500.12627/28643Test
https://doi.org/10.1097/01.mcd.0000052340.43310.a7Test
https://hdl.handle.net/20.500.12627/28643Test
http://www.ncbi.nlm.nih.gov/pubmed/12868484Test

المؤلفون: Gul, D, Unay, B, Akin, R, Ulucan, H

المساهمون: 727140

مصطلحات موضوعية: Tıp, GENETİK VE HAYAT, Moleküler Biyoloji ve Genetik, Yaşam Bilimleri (LIFE), Sağlık Bilimleri, Dahili Tıp Bilimleri, Tıbbi Genetik, Yaşam Bilimleri, Temel Bilimler

العلاقة: CLINICAL DYSMORPHOLOGY; Gul D., Unay B., Ulucan H., Akin R., "Unilateral split foot, torticollis, congenital heart defect and hydrocephaly: a new syndrome?", CLINICAL DYSMORPHOLOGY, cilt.11, sa.2, ss.141-142, 2002; av_12a9842f-57fa-475a-a272-cab214089cab; vv_1032021; http://hdl.handle.net/20.500.12627/17992Test; http://www.ncbi.nlm.nih.gov/pubmed/12002147Test; 11; 141; 142

الإتاحة: https://doi.org/20.500.12627/17992Test
https://hdl.handle.net/20.500.12627/17992Test
http://www.ncbi.nlm.nih.gov/pubmed/12002147Test

المؤلفون: Parry, EM, Ulucan, H, Parry, JM, Corso, C

المساهمون: 728575

مصطلحات موضوعية: İç Hastalıkları, Onkoloji, Tıbbi Genetik, Yaşam Bilimleri, Moleküler Biyoloji ve Genetik, Temel Bilimler, Sağlık Bilimleri, Dahili Tıp Bilimleri, Tıp, Yaşam Bilimleri (LIFE), GENETİK VE HAYAT, Klinik Tıp (MED), Klinik Tıp, ONKOLOJİ

العلاقة: CANCER GENETICS AND CYTOGENETICS; Corso C., Ulucan H., Parry E., Parry J., "Comparative analysis of two thyroid tumor cell lines by fluorescence in situ hybridization and comparative genomic hybridization", CANCER GENETICS AND CYTOGENETICS, cilt.137, ss.108-118, 2002; vv_1032021; av_dc132217-5ece-4e53-bcf1-620e0f5c1b1d; http://hdl.handle.net/20.500.12627/145052Test; http://www.ncbi.nlm.nih.gov/pubmed/12393281Test; https://doi.org/10.1016/s0165-4608Test(02)00562-9; 137; 108; 118

الإتاحة: https://doi.org/20.500.12627/14505210.1016/s0165-4608Test(02)00562-9
https://hdl.handle.net/20.500.12627/145052Test
http://www.ncbi.nlm.nih.gov/pubmed/12393281Test

المؤلفون: Oktenli, C, Ulucan, H, Gul, D, Saglam, M

المساهمون: 727607

مصطلحات موضوعية: Yaşam Bilimleri, Moleküler Biyoloji ve Genetik, Temel Bilimler, Dahili Tıp Bilimleri, Tıbbi Genetik, Sağlık Bilimleri, Tıp, Yaşam Bilimleri (LIFE), GENETİK VE HAYAT

العلاقة: CLINICAL DYSMORPHOLOGY; Oktenli C., Ulucan H., Saglam M., Gul D., "Camptodactyly, skeletal changes, ptosis and infertility in a male: a new syndrome?", CLINICAL DYSMORPHOLOGY, cilt.10, sa.4, ss.295-297, 2001; av_712d3d23-cf68-430d-a565-9a3f8b2dc92e; vv_1032021; http://hdl.handle.net/20.500.12627/77980Test; http://www.ncbi.nlm.nih.gov/pubmed/11666008Test; 10; 295; 297

الإتاحة: https://doi.org/20.500.12627/77980Test
https://hdl.handle.net/20.500.12627/77980Test
http://www.ncbi.nlm.nih.gov/pubmed/11666008Test