Seven M - 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: seven m. 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

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. Turk J Pediatr. 1998 Oct-Dec;40(4):593-601. Turk J Pediatr. 1998. PMID: 10028871

3

N-acetyl-beta-glucosaminidase and beta-galactosidase activity in children receiving antiepileptic drugs.

Yüksel A, Cengiz M, Seven M, Cengiz S, Cenani A. Yüksel A, et al. Among authors: seven m. Pediatr Neurol. 1999 Jan;20(1):24-6. doi: 10.1016/s0887-8994(98)00079-4. Pediatr Neurol. 1999. PMID: 10029255

4

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

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

5

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: seven m. Genet Couns. 1999;10(3):265-9. Genet Couns. 1999. PMID: 10546098

6

Neuroblastoma in a dysmorphic girl with a partial duplication of 2p caused by an unbalanced translocation.

Yuksel A, Seven M, Karaman B, Yilmaz S, Deviren A, Hacihanefioglu S, Basaran S. Yuksel A, et al. Among authors: seven m. Clin Dysmorphol. 2002 Jan;11(1):39-42. doi: 10.1097/00019605-200201000-00008. Clin Dysmorphol. 2002. PMID: 11822704

7

Antioxidant system in Down syndrome: a possible role in cataractogenesis.

Cengiz M, Seven M, Suyugül N. Cengiz M, et al. Among authors: seven m. Genet Couns. 2002;13(3):339-42. Genet Couns. 2002. PMID: 12416643

8

Recessive truncating NALCN mutation in infantile neuroaxonal dystrophy with facial dysmorphism.

Köroğlu Ç, Seven M, Tolun A. Köroğlu Ç, et al. Among authors: seven m. J Med Genet. 2013 Aug;50(8):515-20. doi: 10.1136/jmedgenet-2013-101634. Epub 2013 Jun 7. J Med Genet. 2013. PMID: 23749988

9

Neonatal fractures as a presenting feature of LMOD3-associated congenital myopathy.

Abbott M, Jain M, Pferdehirt R, Chen Y, Tran A, Duz MB, Seven M, Gibbs RA, Muzny D, Lee B, Marom R, Burrage LC. Abbott M, et al. Among authors: seven m. Am J Med Genet A. 2017 Oct;173(10):2789-2794. doi: 10.1002/ajmg.a.38383. Epub 2017 Aug 16. Am J Med Genet A. 2017. PMID: 28815944 Free PMC article.

10

Neuroimaging findings of four patients with Sandhoff disease.

Yüksel A, Yalçinkaya C, Işlak C, Gündüz E, Seven M. Yüksel A, et al. Among authors: seven m. Pediatr Neurol. 1999 Aug;21(2):562-5. doi: 10.1016/s0887-8994(99)00041-7. Pediatr Neurol. 1999. PMID: 10465144

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

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

152 results

Search Page

Filters