Oğur G - Search Results

1

Prenatal diagnosis of autosomal recessive osteopetrosis, infantile type, by X-ray evaluation.

Oğur G, Oğur E, Celasun B, Baser I, Imïrzalioğlu N, Oztürk T, Alemdaroğlu A. Oğur G, et al. Among authors: ogur e. Prenat Diagn. 1995 May;15(5):477-81. doi: 10.1002/pd.1970150512. Prenat Diagn. 1995. PMID: 7644439

2

Application of the 'Apt test' in prenatal diagnosis to evaluate the fetal origin of blood obtained by cordocentesis: results of 30 pregnancies.

Ogur G, Gül D, Ozen S, Imirzalioglu N, Cankus G, Tunca Y, Bahçe M, Güran S, Baser I. Ogur G, et al. Prenat Diagn. 1997 Sep;17(9):879-82. doi: 10.1002/(sici)1097-0223(199709)17:9<879::aid-pd152>3.0.co;2-p. Prenat Diagn. 1997. PMID: 9316136

3

Clinical, ultrastructural and biochemical studies in two sibs with Ehlers-Danlos syndrome type VI-B-like features.

Oğur G, Baykan N, De Paepe A, Steinmann B, Quatacker J, Kuseyrí F, Yüksel-Apak M. Oğur G, et al. Clin Genet. 1994 Dec;46(6):417-22. doi: 10.1111/j.1399-0004.1994.tb04409.x. Clin Genet. 1994. PMID: 7889658

4

Familial trisomy 11p resulting from a balanced paternal translocation: 3 new cases including first trimester diagnosis.

Ogur G, Hayez F, Herinckx A, Van Regemorter N, Vamos E. Ogur G, et al. J Genet Hum. 1988 Aug;36(4):323-9. J Genet Hum. 1988. PMID: 3221208

5

The acrocallosal syndrome in a Turkish boy.

Yüksel M, Caliskan M, Oğur G, Ozmen M, Dolunay G, Apak S. Yüksel M, et al. Among authors: ogur g. J Med Genet. 1990 Jan;27(1):48-9. doi: 10.1136/jmg.27.1.48. J Med Genet. 1990. PMID: 2308155 Free PMC article.

6

Association of syndactyly, ectodermal dysplasia, and cleft lip and palate: report of two sibs from Turkey.

Oğur G, Yüksel M. Oğur G, et al. J Med Genet. 1988 Jan;25(1):37-40. J Med Genet. 1988. PMID: 2832607 Free PMC article. Review.

7

Syndrome of congenital cutis laxa with ligamentous laxity and delayed development: report of a brother and sister from Turkey.

Oğur G, Yüksel-Apak M, Demiryont M. Oğur G, et al. Am J Med Genet. 1990 Sep;37(1):6-9. doi: 10.1002/ajmg.1320370103. Am J Med Genet. 1990. PMID: 1700609

8

Variable clinical expression of Holt-Oram syndrome in three generations.

Oğur G, Gül D, Lenk MK, Imirzalioğlu N, Alpay F, Oğur E. Oğur G, et al. Among authors: ogur e. Turk J Pediatr. 1998 Oct-Dec;40(4):613-8. Turk J Pediatr. 1998. PMID: 10028874

9

657del5 mutation in the NBS1 gene is associated with Nijmegen breakage syndrome in a Turkish family.

Tekin M, Doğu F, Taçyíldiz N, Akar E, Ikincioğullari A, Oğur G, Yavuz G, Babacan E, Akar N. Tekin M, et al. Among authors: ogur g. Clin Genet. 2002 Jul;62(1):84-8. doi: 10.1034/j.1399-0004.2002.620112.x. Clin Genet. 2002. PMID: 12123493

10

[A comparative study of the karyotypes of fetuses of spontaneous early abortions obtained by direct method and by long-term culture].

Ogur G, Debusscher C, Vamos E. Ogur G, et al. J Gynecol Obstet Biol Reprod (Paris). 1990;19(4):427-32. J Gynecol Obstet Biol Reprod (Paris). 1990. PMID: 2380508 French.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

Search Page

Search Results