Balci S - Search Results

1

Down syndrome associated with systemic lupus erythematosus: a mere coincidence or a significant association?

Bakkaloglu A, Ozen S, Besbas N, Saatci U, Balci S. Bakkaloglu A, et al. Among authors: balci s. Clin Genet. 1994 Oct;46(4):322-3. doi: 10.1111/j.1399-0004.1994.tb04170.x. Clin Genet. 1994. PMID: 7834901

2

Noonan syndrome and systemic lupus erythematosus: presentation in childhood.

Alanay Y, Balcı S, Ozen S. Alanay Y, et al. Among authors: balci s. Clin Dysmorphol. 2004 Jul;13(3):161-163. doi: 10.1097/01.mcd.0000127467.04018.6d. Clin Dysmorphol. 2004. PMID: 15194952

3

Diploid-triploid and tetraploid mosaicism in a child with cryptogenic cirrhosis and membranous glomerulonephritis: a causal relationship or coincidental association?

Topaloğlu R, Aktaş D, Bakkaloğlu A, Balci S, Doğru D, Oztürk R. Topaloğlu R, et al. Among authors: balci s. Turk J Pediatr. 1998 Jan-Mar;40(1):139-43. Turk J Pediatr. 1998. PMID: 9673542

4

Dermatological manifestations of 71 Down syndrome children admitted to a clinical genetics unit.

Ercis M, Balci S, Atakan N. Ercis M, et al. Among authors: balci s. Clin Genet. 1996 Nov;50(5):317-20. doi: 10.1111/j.1399-0004.1996.tb02381.x. Clin Genet. 1996. PMID: 9007317

5

A case of Carpenter syndrome diagnosed in a 20-week-old fetus with postmortem examination.

Balci S, Onol B, Eryilmaz M, Haytoglu T. Balci S, et al. Clin Genet. 1997 Jun;51(6):412-6. doi: 10.1111/j.1399-0004.1997.tb02501.x. Clin Genet. 1997. PMID: 9237506

6

Keipert syndrome in two brothers from Turkey.

Balci S, Dagli S. Balci S, et al. Clin Genet. 1996 Oct;50(4):223-8. doi: 10.1111/j.1399-0004.1996.tb02631.x. Clin Genet. 1996. PMID: 9001804

7

Familial intestinal polyatresia syndrome.

Güngör N, Balci S, Tanyel FC, Göğüş S. Güngör N, et al. Among authors: balci s. Clin Genet. 1995 May;47(5):245-7. doi: 10.1111/j.1399-0004.1995.tb04304.x. Clin Genet. 1995. PMID: 7554349

8

Can cytomegalovirus cause brachydactyly? A case report and review of the literature.

Cinbis M, Topcu M, Balci S. Cinbis M, et al. Among authors: balci s. Clin Genet. 1993 Apr;43(4):204-6. doi: 10.1111/j.1399-0004.1993.tb04449.x. Clin Genet. 1993. PMID: 8392455

9

Familial short rib syndrome, type Beemer, with pyloric stenosis and short intestine, one case diagnosed prenatally.

Balci S, Erçal MD, Onol B, Cağlar M, Doğan A, Doğruel N. Balci S, et al. Clin Genet. 1991 Apr;39(4):298-303. doi: 10.1111/j.1399-0004.1991.tb03029.x. Clin Genet. 1991. PMID: 2070548

10

Co-occurrence of chromosome 22q11.2 microdeletion and trisomy 21 mosaicism.

Derbent M, Saygili A, Yilmaz Z, Kervancioğlu M, Balci S, Tokel K. Derbent M, et al. Among authors: balci s. Am J Med Genet. 2002 Sep 15;112(1):99-102. doi: 10.1002/ajmg.10545. Am J Med Genet. 2002. PMID: 12239730

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