TY  - GEN
AU  - TURPIN,R
AU  - LEJEUNE,J
AU  - SALMON,C
TI  - [DISCUSSION OF THE PATERNAL ORIGIN OF THE X CHROMOSOME FROM A TURNER SYNDROME, XO, PROTANOPE AND XG (A-)]
SN  - 0001-4036
PY  - 1996///1201
KW  - Chromosome Aberrations
KW  - Chromosome Disorders
KW  - Chromosomes
KW  - Color Vision Defects
KW  - Genetics, Medical
KW  - Humans
KW  - Turner Syndrome
KW  - X Chromosome
N1  - Publication Type: Journal Article
ER  -