Cenani A - Search Results

1

Anophthalmia-Waardenburg syndrome: a report of three cases.

Suyugül Z, Seven M, Hacihanefioğlu S, Kartal A, Suyugül N, Cenani A. Suyugül Z, et al. Among authors: cenani a. Am J Med Genet. 1996 Apr 24;62(4):391-7. doi: 10.1002/(SICI)1096-8628(19960424)62:4<391::AID-AJMG12>3.0.CO;2-J. Am J Med Genet. 1996. PMID: 8723070

2

Two female siblings with a previously unreported MCA/MR syndrome: pre- and postnatal growth retardation, iris colobomata, spasticity, facial dysmorphism and dilated ventricles.

Yüksel A, Seven M, Deviren A, Söylemez MA, Hacihanefioğlu S, Ulutin T, Cenani A. Yüksel A, et al. Among authors: cenani a. Genet Couns. 1999;10(3):265-9. Genet Couns. 1999. PMID: 10546098

3

Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.

Tüysüz B, Hacihanefioglu S, Silahtaroglu A, Yilmaz S, Deviren A, Cenani A. Tüysüz B, et al. Among authors: cenani a. Genet Couns. 2000;11(4):355-61. Genet Couns. 2000. PMID: 11140413

4

A small supernumerary marker chromosome X identified by in situ hybridization.

Silahtaroglu AN, Hacihanefioglu S, Yilmaz S, Tarkan Y, Cenani A, Tümer Z. Silahtaroglu AN, et al. Among authors: cenani a. Clin Genet. 1995 May;47(5):270-3. doi: 10.1111/j.1399-0004.1995.tb04310.x. Clin Genet. 1995. PMID: 7554355

5

Not para-, not peri-, but centric inversion of chromosome 12.

Silahtaroglu AN, Hacihanefioglu S, Güven GS, Cenani A, Wirth J, Tommerup N, Tümer Z. Silahtaroglu AN, et al. Among authors: cenani a. J Med Genet. 1998 Aug;35(8):682-4. doi: 10.1136/jmg.35.8.682. J Med Genet. 1998. PMID: 9719380 Free PMC article.

6

A family presenting Goltz syndrome (focal dermal hypoplasia) in three generations.

Seven M, Suyugül Z, Yüksel A, Geçkinli B, Hacihanefioğlu S, Cenani A. Seven M, et al. Among authors: cenani a. Turk J Pediatr. 1998 Oct-Dec;40(4):593-601. Turk J Pediatr. 1998. PMID: 10028871

7

Mohr-Majewski syndrome (orofaciodigital syndrome type IV) in five sibs.

Tüysüz B, Arapoğlu M, Seven M, Cenani A. Tüysüz B, et al. Among authors: cenani a. Genet Couns. 1999;10(2):189-92. Genet Couns. 1999. PMID: 10422014

8

Glutathione and related enzymes in rat liver treated with methyl nitrosourea.

Cengiz M, Hacihanefioglu S, Cenani A. Cengiz M, et al. Among authors: cenani a. J Basic Clin Physiol Pharmacol. 1996;7(4):341-5. doi: 10.1515/jbcpp.1996.7.4.341. J Basic Clin Physiol Pharmacol. 1996. PMID: 9080308

9

Waardenburg syndrome: variable phenotypic expression in monozygotic twins.

Suyugül Z, Tüysüz B, Tükenmez F, Başaran M, Cenani A. Suyugül Z, et al. Among authors: cenani a. Clin Dysmorphol. 1998 Jan;7(1):77-8. Clin Dysmorphol. 1998. PMID: 9546839 No abstract available.

10

Expression of aphidicolin, FUdR and caffeine-induced fragile sites in lymphocytes of healthy Turkish individuals.

Güven GS, Hacihanefioğlu S, Cenani A. Güven GS, et al. Among authors: cenani a. Genetica. 1999;105(1):109-16. doi: 10.1023/a:1003799927024. Genetica. 1999. PMID: 10483096

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