A deletion mutation of the connexin 26 (Gjb2) gene in a Turkish patient with vohwinkel syndrome

Traditionally, women with hypogonadotropic hypogonadism (HH) were considered to be at lower risk for the development of ovarian hyperstimula- tion syndrome (OHSS), although

Identifi- cation of an ancestral haplotype of the 35delG mutation in the GJB2 (connexin 26) gene responsible for autosomal recessive non -syndromic hearing loss in

Çal %mada, Türkiye’deki seyahat acenteleri çal %anlar n n hizmet kalitesi konusundaki alg lamalar n belirlemek için Bigne ve arkada%lar taraf ndan seyahat acentelerine uyarlanm

Yeni gelişmeler ve özellikle sivil-asker işbirliği ile silahlı kuvvetler arasındaki etkileşimin artmasıyla birlikte sert güç aracı olarak silahlı kuvvetlerin yumuşak

This study revealed that the physicians’ perceptions on quality of care under the case payment system are influenced by the ph ysicians’ hospital characteristics (hospital

SF 36 Yaşam kalitesi ölçeğinin tüm alt alanlarına bakıldığında bedensel ve ruhsal sağlık durumlarını iyi hissedenlerin ölçek puanları, kötü hissedenlere göre

Acute arthralgia was developed two weeks ago and then painful, aphthous oral ulcer, circinate vulvitis and psoriasiform hyperkeratotic eruption (keratoderma

Dilated cardiomyopathy with woolly hair and keratoderma (DCWHK), also known as Carvajal disease, is an autosomal re- cessive cardio-cutaneous syndrome caused by mutations in DSP,