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Papers authored by Bökesoy I

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An unusual combination: aortic arch coarctation associated with Dandy-Walker variant.

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Akgul A, Babaroglu S, Bahar I, Bokesoy I, Birincioğlu L, and Cobanoglu A

International journal of cardiology 113(2):258-60, 2006 Nov 10 - Who cited this? | PubMed ID: 16297468 | Fulltext

Aldolase B mutations in Turkish families from central Anatolia.

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Karabulut HG, Halsall D, Sayin BD, Tonyukuk V, Cox TM, and Bökesoy I

Genetic counseling (Geneva, Switzerland) 17(4):457-60, 2006 - Who cited this? | PubMed ID: 17375533 | Fulltext

DNMT3B mutations and DNA methylation defect define two types of ICF syndrome.

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Jiang YL, Rigolet M, Bourc'his D, Nigon F, Bokesoy I, Fryns JP, Hultén M, Jonveaux P, Maraschio P, Mégarbané A, Moncla A, and Viegas-Péquignot E

Human mutation 25(1):56-63, 2005 Jan - Who cited this? | PubMed ID: 15580563 | Fulltext

The role of genetic counseling on decisions of pregnant women aged 35 years or over regarding amniocentesis in Turkey.

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Ilgin-Ruhi H, Yürür-Kutlay N, Tükün A, and Bökesoy I

European journal of medical genetics 48(1):13-9, 2005 - Who cited this? | PubMed ID: 15953401 | Fulltext

Is SHORT syndrome another phenotypic variation of PITX2?.

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Karadeniz NN, Kocak-Midillioglu I, Erdogan D, and Bökesoy I

American journal of medical genetics. Part A 130(4):406-9, 2004 Nov 1 - Who cited this? | PubMed ID: 15481036 | Fulltext

Y-STR polymorphism in Central Anatolian Region of Turkey.

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Rustamov A, Gümüş G, Karabulut HG, Elhan AH, Kadikiran A, and Bökesoy I

Forensic science international 139(2-3):227-30, 2004 Jan 28 - Who cited this? | PubMed ID: 15040921 | Fulltext

A 15-year-old boy with Rubinstein-Taybi syndrome associated with severe congenital malalignment of the toenails.

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Balci S, Bostanci S, Ekmekci P, Cebeci I, Bokesoy I, Bartsch O, and Gurgey E

Pediatric dermatology 21(1):44-7, 2004 - Who cited this? | PubMed ID: 14871325 | Fulltext

46, XY gonadal dysgenesis and chronic renal failure: first reported case with Frasier syndrome from Turkey.

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Karabulut HG, Sayin BD, and Bökesoy I

Genetic counseling (Geneva, Switzerland) 15(4):489-91, 2004 - Who cited this? | PubMed ID: 15658629 | Fulltext

Macrodystrophia lipomatosa of the feet and subcutaneous lipomas.

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Aydos SE, Fitoz S, and Bökesoy I

American journal of medical genetics. Part A 119(1):63-5, 2003 May 15 - Who cited this? | PubMed ID: 12707961 | Fulltext

Gonadal dysgenesis and the Mayer-Rokitansky-Kuster-Hauser syndrome in a girl with 46,X,del(X)(pter-->q22:).

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Aydos S, Tükün A, and Bökesoy I

Archives of gynecology and obstetrics 267(3):173-4, 2003 Jan - Who cited this? | PubMed ID: 12552332 | Fulltext

The impact of vitamin D receptor genotype on the management of anemia in hemodialysis patients.

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Ertürk S, Kutlay S, Karabulut HG, Keven K, Nergizoglu G, Ates K, Bokesoy I, and Duman N

American journal of kidney diseases : the official journal of the National Kidney Foundation 40(4):816-23, 2002 Oct - Who cited this? | PubMed ID: 12324918 | Fulltext

Common fragile sites associated with the breakpoints of chromosomal aberrations in hematologic neoplasms.

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Gümüş G, Sunguroğlu A, Tükün A, Sayin DB, and Bökesoy I

Cancer genetics and cytogenetics 133(2):168-71, 2002 Mar - Who cited this? | PubMed ID: 11943347 | Fulltext

Whistling face syndrome with normal hands and feet.

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Toydemir PB, Toydemir R, and Bokesoy I

American journal of medical genetics 102(2):215, 2001 Aug 1 - Who cited this? | PubMed ID: 11477620 | Fulltext

A Down syndrome case with a karyotype of 46,XY,rec(21)dup(21q)inv(21)(p11q22) derived from paternal pericentric inversion of chromosome 21.

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Ilgin Ruhi H, Tükün A, Karabulut H, Bayazit P, and Bökesoy I

Clinical genetics 59(5):368-70, 2001 May - Who cited this? | PubMed ID: 11359472 | Fulltext

Butterfly vertebra: a case report.

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Sonel B, Yalçin P, Oztürk EA, and Bökesoy I

Clinical imaging 25(3):206-8, 2001 - Who cited this? | PubMed ID: 11679230 | Fulltext

Mental retardation with rare fragile site expressed at 2q11.

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Tükün A, Renda Y, Topçu M, Tuncali T, and Bökesoy I

Brain & development 22(8):498-500, 2000 Dec - Who cited this? | PubMed ID: 11111064 | Fulltext

Effects of factor V gene G1691A, methylenetetrahydrofolate reductase gene C677T, and prothombin gene G20210A mutations on deep venous thrombogenesis in Behçet's disease.

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Toydemir PB, Elhan AH, Tükün A, Toydemir R, Gürler A, Tüzüner A, and Bökesoy I

The Journal of rheumatology 27(12):2849-54, 2000 Dec - Who cited this? | PubMed ID: 11128675 | Fulltext

Relation between the insertion/deletion polymorphism of the angiotensin I converting enzyme gene and restenosis after coronary stenting.

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Gürlek A, Güleç S, Karabulut H, Bokesoy I, Tutar E, Pamir G, Alpman A, Toydemir R, Aras O, and Oral D

Journal of cardiovascular risk 7(6):403-7, 2000 Dec - Who cited this? | PubMed ID: 11155292 | Fulltext

Essay on the nucleoli survey by the alpha- and beta-satellite DNA probes of the acrocentric chromosomes in mitogen-stimulated human lymphocytes.

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Demirtas H, Candemir Z, Cücer N, Imamoglu N, Dönmez H, and Bökesoy I

Annales de genetique 43(2):61-8, 2000 - Who cited this? | PubMed ID: 10998446 | Fulltext

Whistling face phenotype without limb abnormalities.

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Toydemir PB, Toydemir R, and Bökesoy I

American journal of medical genetics 86(1):86-7, 1999 Sep 3 - Who cited this? | PubMed ID: 10440836 | Fulltext

Urinary cyclophosphamide excretion and micronuclei frequencies in peripheral lymphocytes and in exfoliated buccal epithelial cells of nurses handling antineoplastics.

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Burgaz S, Karahalil B, Bayrak P, Taşkin L, Yavuzaslan F, Bökesoy I, Anzion RB, Bos RP, and Platin N

Mutation research 439(1):97-104, 1999 Feb 2 - Who cited this? | PubMed ID: 10029685 | Fulltext

Molecular alterations in the TP53 gene of peripheral blood cells of patients with chronic myeloid leukemia.

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Peller S, Yona R, Kopilova Y, Prokocimer M, Goldfinger N, Uysal A, Karabulut HG, Tukun A, Bokesoy I, Tuncman G, and Rotter V

Genes, chromosomes & cancer 21(1):2-7, 1998 Jan - Who cited this? | PubMed ID: 9443036 | Fulltext

Identification of the parental origin of polysomy in two 49,XXXXY cases.

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Celik A, Eraslan S, Gökgöz N, Ilgin H, Başaran S, Bökesoy I, Kayserili H, Yüksel-Apak M, and Kirdar B

Clinical genetics 51(6):426-9, 1997 Jun - Who cited this? | PubMed ID: 9237509 | Fulltext

Null alleles of the aldolase B gene in patients with hereditary fructose intolerance.

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Ali M, Tunçman G, Cross NC, Vidailhet M, Bökesoy I, Gitzelmann R, and Cox TM

Journal of medical genetics 31(6):499-503, 1994 Jun - Who cited this? | PubMed ID: 8071980 | Fulltext

Orbito-ocular granulocytic sarcoma (OOGS) and acute myeloblastic leukemia (AML) with duplication of Philadelphia chromosome.

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Cavdar AO, Bökesoy I, Sunguroğlu A, Yavuz G, Tanindi S, Gözdaşoğlu S, Babacan E, Pamĭr A, Unal E, and Türker A

Cancer genetics and cytogenetics 69(1):38-40, 1993 Aug - Who cited this? | PubMed ID: 8374898 | Fulltext

A case of Prader Willi syndrome with del 15 (q11-->q13).

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Tunçman G, Tükün A, Yalaz K, and Bökesoy I

The Turkish journal of pediatrics 35(4):333-6, 1993 - Who cited this? | PubMed ID: 8160287 | Fulltext

Taste sensitivity to phenylthiocarbamide in Turkey.

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Bökesoy I and Togan I

Gene geography : a computerized bulletin on human gene frequencies 1(2):99-101, 1987 Aug - Who cited this? | PubMed ID: 3154119 | Fulltext

A case of achondrogenesis type I.

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Bökesoy I, Aydin E, and Gazilerli S

Human genetics 67(3):349-50, 1984 - Who cited this? | PubMed ID: 6469245 | Fulltext

Oromandibular limb hypogenesis/Hanhart's syndrome: possible drug influence on the malformation.

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Bökesoy I, Aksüyek C, and Deniz E

Clinical genetics 24(1):47-9, 1983 Jul - Who cited this? | PubMed ID: 6616945 | Fulltext

A case of SC-phocomelia syndrome with nonrandom centromere separation.

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Bökesoy I, Balci S, and Bilgiç S

Progress in clinical and biological research 104:351-8, 1982 - Who cited this? | PubMed ID: 7163280 | Fulltext

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