-
Peters anomaly (sequence analysis of PITX2 gene)
+ info
-
Peters-plus syndrome (frequent mutations of B3GALTL gene)
+ info
-
Peters-plus syndrome (sequence analysis of B3GALTL gene)
+ info
-
Peutz-Jeghers syndrome (deletion/duplication analysis on STK11 gene)
+ info
-
Peutz-Jeghers syndrome (sequence analysis of STK11 gene)
+ info
-
Pfeiffer syndrome (deletion/duplication analysis of FGFR1 gene)
+ info
-
Pfeiffer syndrome (deletion/duplication analysis of FGFR2 gene)
+ info
-
Pfeiffer syndrome (sequence analysis of FGFR1 and FGFR2 genes)
+ info
-
Pfeiffer syndrome (sequence analysis of FGFR1 gene)
+ info
-
Pharmacogenetics of antiangiogenics in ophthalmology (detection of p.Y402H variant in CFH gene)
+ info
-
Phelan-McDermid syndrome (deletion/duplication analysis on SHANK3 gene)
+ info
-
Phenylketonuria (deletion/duplication analysis of PAH gene)
+ info
-
Phenylketonuria (sequence analysis of PAH gene)
+ info
-
Pheochromocytoma (sequence analysis of MAX gene)
+ info
-
Pheochromocytoma (sequence analysis of SDHB gene)
+ info
-
Pheochromocytoma (sequence analysis of SDHD gene)
+ info
-
Pheochromocytoma (sequence analysis of VHL gene)
+ info
-
Pheochromocytoma and paraganglioma (NGS panel of 17 genes)
+ info
-
Pheochromocytomas (NGS panel for 3 genes)
+ info
-
Phosphoglycerate dehydrogenase deficiency (sequence analysis of PHGDH gene)
+ info
