Tüysüz B - Search Results

1

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

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

2

Hypoglossia-hypodactylia (Hanhart's) syndrome with sensorineural hearing loss.

Tüysüz B, Erginel A, Unutmaz T, Cenani A. Tüysüz B, et al. Turk J Pediatr. 1994 Oct-Dec;36(4):347-52. Turk J Pediatr. 1994. PMID: 7825244

3

Polydactyly and fetal hydantoin syndrome: an additional component of the syndrome?

Yalçinkaya C, Tüysüz B, Somay G, Cenani A. Yalçinkaya C, et al. Among authors: tuysuz b. Clin Genet. 1997 May;51(5):343-5. doi: 10.1111/j.1399-0004.1997.tb02485.x. Clin Genet. 1997. PMID: 9212184

4

Waardenburg syndrome: variable phenotypic expression in monozygotic twins.

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

5

Meckel-Gruber syndrome.

Gazioğlu N, Vural M, Seçkin MS, Tüysüz B, Akpir E, Kuday C, Ilikkan B, Erginel A, Cenani A. Gazioğlu N, et al. Among authors: tuysuz b. Childs Nerv Syst. 1998 Mar;14(3):142-5. doi: 10.1007/s003810050198. Childs Nerv Syst. 1998. PMID: 9579873

6

Picture of the month. Keutel syndrome.

Tüysüz B, Ungür S, Akalin F, Cenani A, Tunnessen WW Jr. Tüysüz B, et al. Arch Pediatr Adolesc Med. 1999 Jul;153(7):765-6. doi: 10.1001/archpedi.153.7.765. Arch Pediatr Adolesc Med. 1999. PMID: 10401814 No abstract available.

7

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. Genet Couns. 2000;11(4):355-61. Genet Couns. 2000. PMID: 11140413

8

Is the novel SCKL3 at 14q23 the predominant Seckel locus?

Kilinç MO, Ninis VN, Ugur SA, Tüysüz B, Seven M, Balci S, Goodship J, Tolun A. Kilinç MO, et al. Among authors: tuysuz b. Eur J Hum Genet. 2003 Nov;11(11):851-7. doi: 10.1038/sj.ejhg.5201057. Eur J Hum Genet. 2003. PMID: 14571270

9

Congenital cutis laxa syndrome: type II autosomal recessive inheritance.

Tüysüz B, Arapoğlu M, Ilikkan B, Demirkesen C, Perk Y. Tüysüz B, et al. Turk J Pediatr. 2003 Jul-Sep;45(3):265-8. Turk J Pediatr. 2003. PMID: 14696810

10

Spondyloenchondrodysplasia: clinical variability in three cases.

Tüysüz B, Arapoglu M, Ungür S. Tüysüz B, et al. Am J Med Genet A. 2004 Jul 15;128A(2):185-9. doi: 10.1002/ajmg.a.30078. Am J Med Genet A. 2004. PMID: 15214014

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