Bagci G - Search Results

1

Hypogammaglobulinemia and Silver-Russell phenotype associated with partial trisomy 7q and partial monosomy 21q.

Artac H, Reisli I, Yildirim MS, Bagci G, Luleci G, Hosgor O, Karaaslan S. Artac H, et al. Among authors: bagci g. Am J Med Genet A. 2009 Feb;149A(2):277-9. doi: 10.1002/ajmg.a.32617. Am J Med Genet A. 2009. PMID: 19161136 No abstract available.

2

Maternal origin and clinical findings in a case with trisomy 22.

Mihçi E, Taçoy S, Yakut S, Ongun H, Keser I, Kiliçarslan B, Bağci G, Lüleci G. Mihçi E, et al. Among authors: bagci g. Turk J Pediatr. 2007 Jul-Sep;49(3):322-6. Turk J Pediatr. 2007. PMID: 17990591

3

Complete gonadal dysgenesis 46,XY (Swyer syndrome) in two sisters and their mother's maternal aunt with a female phenotype.

Bagci G, Bisgin A, Karauzum SB, Trak B, Luleci G. Bagci G, et al. Fertil Steril. 2011 Apr;95(5):1786.e1-3. doi: 10.1016/j.fertnstert.2010.11.034. Epub 2010 Dec 9. Fertil Steril. 2011. PMID: 21145048 Free article.

4

Bloom's syndrome in a Turkish individual.

Yilmaz E, Alpsoy E, Lüleci G, Bağci G, Yilmaz GG, Cetin L, Başaran E. Yilmaz E, et al. Among authors: bagci g. Clin Genet. 1996 Jun;49(6):314-5. doi: 10.1111/j.1399-0004.1996.tb03796.x. Clin Genet. 1996. PMID: 8884082 No abstract available.

5

M-FISH applications in clinical genetics.

Cetin Z, Berker Karaüzüm S, Yakut S, Mihçi E, Baumer A, Wey E, Taçoy S, Bağci G, Lüleci G. Cetin Z, et al. Among authors: bagci g. Genet Couns. 2005;16(3):257-68. Genet Couns. 2005. PMID: 16259323

6

Prenatal diagnosis of β-thalassemia and other hemoglobinopathies in southwestern Turkey.

Mendilcioglu I, Yakut S, Keser I, Simsek M, Yesilipek A, Bagci G, Luleci G. Mendilcioglu I, et al. Among authors: bagci g. Hemoglobin. 2011;35(1):47-55. doi: 10.3109/03630269.2010.544607. Hemoglobin. 2011. PMID: 21250881

7

Triploidy in a growth discordant twin pregnancy after intracytoplasmic sperm injection treatment. Case report.

Mendilcioglu I, Ozcan M, Bagci G, Simsek M, Kursun S, Luleci G, Taskin O. Mendilcioglu I, et al. Among authors: bagci g. Fetal Diagn Ther. 2006;21(1):65-7. doi: 10.1159/000089050. Fetal Diagn Ther. 2006. PMID: 16354978

8

A hereditary bisatellite-dicentric supernumerary chromosome in a case of cat-eye syndrome.

Lüleci G, Bağci G, Kivran M, Lüleci E, Bektaş S, Başaran S. Lüleci G, et al. Among authors: bagci g. Hereditas. 1989;111(1):7-10. doi: 10.1111/j.1601-5223.1989.tb00369.x. Hereditas. 1989. PMID: 2793513 Free article.

9

The effect of hydroxyurea on rabbit subconjunctival fibroblast culture and use of hydroxyurea in rabbits after glaucoma filtration surgery.

Yücel I, Bagci G, Duranoglu Y, Oztürk A, Aksu G, Lüleci G. Yücel I, et al. Among authors: bagci g. Ophthalmologica. 1999;213(5):311-9. doi: 10.1159/000027445. Ophthalmologica. 1999. PMID: 10516520

10

Parental origin and mechanisms of formation of cytogenetically recognisable de novo direct and inverted duplications.

Kotzot D, Martinez MJ, Bagci G, Basaran S, Baumer A, Binkert F, Brecevic L, Castellan C, Chrzanowska K, Dutly F, Gutkowska A, Karaüzüm SB, Krajewska-Walasek M, Luleci G, Miny P, Riegel M, Schuffenhauer S, Seidel H, Schinzel A. Kotzot D, et al. Among authors: bagci g. J Med Genet. 2000 Apr;37(4):281-6. doi: 10.1136/jmg.37.4.281. J Med Genet. 2000. PMID: 10745046 Free PMC article.

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