Deletion analysis and clinical correlations in patients with Xp21 linked muscular dystrophy.

Ayfer Ülgenalp,Özlem Giray,Elçin Bora,Tülin Hizli,Semra Hiz Kurul,Gül Sağin-Saylam,Hatice Karasoy,Nedret Uran,Gülşen Dizdarer,Sarenur Tutuncuoglu,Eray Dirik,Ferda Ozkinay,Derya Erçal

Deletion analysis and clinical correlations in patients with Xp21 linked muscular dystrophy.

2004

Ayfer Ülgenalp
Özlem Giray
Elçin Bora
Tülin Hizli
Semra Hiz Kurul
Gül Sağin-Saylam
Hatice Karasoy
Nedret Uran
Gülşen Dizdarer
Sarenur Tutuncuoglu
Eray Dirik
Ferda Ozkinay
Derya Erçal

Ayfer Ulgenalp1, Ozlem Giray1, Elcin Bora1, Tulin Hýzlý2, Semra Kurul1, Gul Saðýn-Saylam1 Hatice Karasoy3, Nedret Uran2, Gulþen Dizdarer4, Sarenur Tutuncuoðlu5, Eray Dirik1 Ferda Ozkýnay5, Derya Ercal1 1Department of Pediatrics, Dokuz Eylul University Faculty of Medicine, 2Behcet Uz Childrens Hospital, Departments of 3Neurology, and 5Pediatrics, Ege University Faculty of Medicine and 4Social Security Tepecik Teaching Hospital, Ýzmir, Turkey

Keywords:

Intensive care medicine
Muscular dystrophy
Physical therapy
Medicine
Genotype
Exon
in patient
Phenotype
Intron
Dystrophin
Diabetes mellitus
Bioinformatics

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