مزود الخدمة
مختبرات الحياة الطبية - ينبع
Showing 127 to 147 of 605 entries
فحص
Congenital Adrenal hyperplasia (CYP21A2 21-hydroxy
...
فحص
Anti Myeloperoxidase Abs (MPO)
...
فحص
Cornelia-De-Lange syndrome Panel (HDAC8, NIPBL, RA
...
فحص
Multiple joint dislocations, short stature, cranio
...
فحص
Cystic fibrosis Middle East Panel of common (CFTR)Cystic fibrosis Middle East Panel of common (CFTR)
...
فحص
Lead in blood
...
فحص
frontometaphyseal dysplasia (FLNA) Sequencing
...
فحص
Fructose-1,6-bisphosphatase deficiency (FBP1) Sequ
...
فحص
Fructose-1,6-bisphosphatase deficiency (FBP1) Dele
...
فحص
Galactosemia (GALT) Sequencing
...
فحص
Gaucher disease (GBA) Sequencing
...
فحص
Glycogen storage diseases Basic Panel (G6PC, SLC37
...
فحص
Deafness, non-syndromic sensorineural autosomal re
...
فحص
Deafness, non-syndromic sensorineural autosomal do
...
فحص
Joubert syndrome gene Panel (26 genese) sequencing
...
فحص
Joubert syndrome gene Panel (26 genese) by Deletio
...
فحص
Mitochondrial diseases gene Panel (22 genesf) sequ
...
فحص
Mitochondrial diseases gene Panel (22 genesf) by D
...
فحص
Hypoparthyroidism-retardation-dysmorphism (Sanjad-
...
فحص
AIRE gene (Autoimmune polyendocrinopathy syndrome
...
فحص
Neutropenia, severe congenital type 1 or cyclic ne
...