2Scapoli C, Collins A, MartineUi M, et al. Combined segregation and linkage analysis of nonsyndromic orofacial cleft in two candidate regions[ J]. Ann Hum Genet, 1999,63 : 17 - 25. 被引量：1
3Braybrook C, Warry G, Howell G, et al. Identification and haracterization of KLHL4, a novel human homologue of the Drosophila Kelch gene that maps within the X - linked cleft palate and Ankyloglossia (CPX) critical region[J]. Genomies, 2001,72(2) :128 -136. 被引量：1
5Marazita ML,Murray JC,Lidral AC,et al. Meta -analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel locion 9q21 and 2p32 -35[J]. Am J Hum Genet,2004,75 (2) :161 - 173. 被引量：1
6Lidral AC, Moreno LM. Progress toward discerning the Genetics of cleft lip[J]. Curr Opin Pediatr,2005,17(6) :731 -739. 被引量：1
7Vieira AR, Avila JR, Daack - Hirsch S, et al. Medical sequencing of candidate genes for nonsyndromic cleft lip and palate[ J]. POLSGenet,2005,1(6) :e64. 被引量：1
2[1]Munger RG, Lidral AC, Basart AM, et al. The Msx-1 homeobox gene and risk of isolated orofacial clefts: an effect modified by maternal vitamin use [J]. Am J Epidemiol, 1995,141(S):74. 被引量：1
3[2]Chenevix-trench G, Jones K, Green AC, et al. Cleft with or without cleft palate: associations with transforming growth factor alpha and retinoic acid receptor loci [J]. Am J Hum Genet, 1992,51(5):1377. 被引量：1
4[3]Itikala PR, Watkins ML, Mulinare J, et al. Maternal multivitamin use and orofacial clefts in offspring [J]. Teratology, 2001,63:79-86. 被引量：1
5[4]Frosst P, Blom HJ, Milos R, et al. A candidate risk factor for vascular disease: a common mutation in methylenetrahydrofolate reductase [J]. Nature Genet, 1995,10:111-113. 被引量：1
6[5]Prescott NJ, Winter RM, Malcolm S. Maternal MTHFR genotype contributes to the risk of non-syndromic cleft lip and palate [J]. J Med Genet, 2002,39(5):368-377. 被引量：1
7[6]Blanto SH, Kolle BS, Hecht JT, et al. No evidence supporting MTHFR as a risk factor in the development of familial NSCLP [J]. Am J Med Genet, 2000,92(5):370-371. 被引量：1
8[7]Martinelli M, Scapoli L, Pezzetti F, et al. C667T variant form at the MTHFR gene and CL/P: a risk factor for mothers [J]. Am J Med Genet, 2001,98(4):357-360. 被引量：1
