Smeeta Gajendra, Ranjit Sahoo
Objective: Autosomal recessive cutis laxa type IIA (ARCL2A) is a rare congenital disorder characterized by loose and elastic skin, growth and developmental delay, and skeletal anomalies. It is caused by biallelic mutatio...
Smeeta Gajendra, Ranjit Sahoo (2015). Kronik Miyelomonositik Lösemide Auer Çubukları Tanıyı Değiştirebilir. Turkish Journal of Hematology, 32(3), 278-279. https://europub.co.uk/articles/-A-95292
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Hiperkalsemi Saptanan Hemodiyaliz Hastasında Nonsekretuar Multipl Miyelom Tanısı
A Novel ATP6V0A2 Mutation Causing Recessive Cutis Laxa with Unusual Manifestations of Bleeding Diathesis and Defective Wound Healing
Objective: Autosomal recessive cutis laxa type IIA (ARCL2A) is a rare congenital disorder characterized by loose and elastic skin, growth and developmental delay, and skeletal anomalies. It is caused by biallelic mutatio...
İntravenöz Siklosporin ile Anafilaksiye Giren ve Oral Formu Tolere Eden Bir Pediatrik Olgu
An Updated Review of Abnormal Hemoglobins in the Turkish Population
Koroner Arter Stent Hastasında Klopidogrel İlişkili Erken Derin Otoimmün Trombositopeni