Clinical dysmorphology
Rafiq syndrome in a Saudi patient: novel homozygous MAN1B1 variant (c.1118C>G; p.Pro373Arg) and expanded phenotypic spectrum.
Zuhair Rahbeeni, Munirah AlSalman, Saad AlHamoudi
Published: 202510.1097/MCD.0000000000000543
No abstract available for this study.