共 18 条
[1]
Medium-chain Acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-Based prospective screening of newborns differ from those observed in patients with clinical symptoms: Identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency
[J].
AMERICAN JOURNAL OF HUMAN GENETICS,
2001, 68 (06)
:1408-1418
[2]
[Anonymous], 1994, RADON RENTAL HOUSING
[3]
*COMM STUD INB ERR, 1975, GEN SCREEN PROGR PRI
[9]
Kritz Francesca Lunzer, 2002, WASH POST, pF1