TY  - GEN
AU  - Vérin,P
TI  - [Atypical congenital achromatopsia (deutanoid monochromasia) and renal malformation]
SN  - 0081-1270
PY  - 1971///0505
KW  - Color Vision Defects
KW  - complications
KW  - Female
KW  - Humans
KW  - Kidney
KW  - abnormalities
KW  - Middle Aged
N1  - Publication Type: Journal Article
ER  -