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The Utility of Next-Generation Sequencing for Primary Immunodeficiency Disorders: Experience from a Clinical Diagnostic Laboratory.Interaction of CD200 Overexpression on Tumor Cells with CD200R1 Overexpression on Stromal Cells: An Escape from the Host Immune Response in Rectal Cancer PatientsHyperphosphatemic Familial Tumoral Calcinosis in Two Siblings with a Novel Mutation in Gene: Experience from Southern TurkeyA homozygote novel L451W mutation in CECR1 gene causes deficiency of adenosine deaminase 2 in a pediatric patient representing with chronic lymphoproliferation and cytopeniaMEFV gene variants in children with Henoch-Schönlein purpura and association with clinical manifestations: a single-center Mediterranean experienceCongenital erythropoietic porphyria with erythrodontia: A case reportBRCA mutation characteristics in a series of index cases of breast cancer selected independent of family historyRecurrent macroscopic hematuria in a pediatric patient: is it early to diagnose as having type I hereditary C2 deficiency?
P50
Q55252308-5C7BE0D2-F73C-43DA-BCFA-07B68F12AFCBQ64230704-C9209B5A-D7DE-4969-9BA2-2F1EA5F7E746Q64235821-15071C81-2C6F-4ADC-9B58-8C1B899BC65EQ90113099-DC3D3224-B2C4-4CDB-BAD2-E4FC30B1B352Q90249068-ABB2DBF3-1235-4687-AF28-49E645626046Q91301254-2176563A-FDE1-4709-8CF7-E7B7E828AAFFQ92952471-2FC48D1B-E485-4FCD-A226-14C7A31E5B12Q94557070-37A5DFFF-7BE1-48E2-8703-CAB0CB97B333
P50
description
researcher
@en
name
Atil Bisgin
@en
type
label
Atil Bisgin
@en
prefLabel
Atil Bisgin
@en
P31
P496
0000-0002-2053-9076