TY  - BOOK
AU  - Pearson Karl Editor
ED  - University of London, Francis Galton Laboratory
TI  - Treasury of human inheritance
U1  - 575.1 
PY  - 1922///
CY  - LOndon
PB  - Cambridge University Press
KW  - Human inheritance
N1  - Pt. I - Retinitis pigmentosa and allied diseases congenital stationary night blindness glioma retinae; Pt. II - Colour blindness; Pt. III -Blue sclerotics and fragility of bone; Pt. IV - Hereditary optic atrophy (Leber's disease)
ER  -