Journal Publications
- [41]Tan YQ*, Lin G, Lu GX, Wang YY, Zhang XX, Huang H, Gong F, Du J, Meng LL, Banerjee S, He WB.He WB, Banerjee S, Meng LL, Du J, Gong F, Huang H, Zhang XX, Wang YY, Lu GX, Lin G, Tan YQ*. Whole-exome sequencing identifies a homozygous donor splice-site mutation in STAG3 that causes primary ovarian insufficiency[J].Clin Genet, 2018, 93 (2) : 340-344.
- [42]Du J, Lin G, Lu GX, Gong F, Luo KL, Xiong B, Li W, Hu X, Tan YQ*, He WB.He WB, Tan YQ, Hu X, Li W, Xiong B, Luo KL, Gong F, Lu GX, Lin G, Du J. Expanded carrier screening and preimplantation genetic diagnosis in a couple who delivered a baby affected with congenital factor VII deficiency[J].BMC Med Genet, 2018, 19 (1) : 15-21.
- [43]Tan YQ*, Lu GX, Liang P, Li W, Du J, Tu CF, Zhang Y, Meng LL, Yuan SM.Yuan SM, Meng LL, Zhang Y, Tu CF, Du J, Li W, Liang P, Lu GX, Tan YQ*. Genotype-phenotype correlation and identification of two novel SRD5A2 mutations in 33 Chinese patients with hypospadias[J].Steroids, 2017, 125: 61-66.
- [44]Zhang H, Jiang F, Chen F, Yuan Y, Peng H, Li W, Li J, Du J, Yin X, Li X, Fu M, Lin G, Gao Y, Tan Y*.Tan Y, Gao Y, Lin G, Fu M, Li X, Yin X, Du J, Li J, Li W, Peng H, Yuan Y, Chen F, Jiang F, Zhang H, Lu G, Gong F, Wang W. Noninvasive prenatal testing (NIPT) in twin pregnancies with treatment of assisted reproductive techniques (ART) in a single center[J].Prenat Diagn, 2016, 36 (7) : 672-679.
- [45]Chen SP, Chen F, Pan XY, Zhang CL, Gong F, Xiong B, Li J, Tan K, Jiang H, Zhang SP, Yin XY, Tan YQ.Tan YQ, Yin XY, Zhang SP, Jiang H, Tan K, Li J, Xiong B, Gong F, Zhang CL, Pan XY, Chen F, Chen SP, Gong C, Lu CF, Luo KL, Gu YF, Zhang XQ, Wang W, Xu X, Vajta G, Bolund L, Yang HM, Lu GX, Du YT, Lin G. Clinical outcome of preimplantation genetic diagnosis and screening using next generation sequencing[J].Gigascience, 2014, 3 (30) : 1-9.
- [46]Tan YQ*, Lin G, Lu GX, Zhong CG, Tan K, Cheng DH, Zhang YN, Xu F.Xu F, Zhang YN, Cheng DH, Tan K, Zhong CG, Lu GX, Lin G, Tan YQ*. The first patient with a pure 1p36 microtriplication associated with severe clinical phenotypes[J].Mol Cytogenet, 2014, 7 (1) : 64-69.
- [47]Lu GX etc, Tang XC, Lu CF, Xiong B, Cheng DH, Gong F, Zhang SP, Tan K, Tan YQ*.Tan YQ, Tan K, Zhang SP, Gong F, Cheng DH, Xiong B, Lu CF, Tang XC, Luo KL, Lin G, Lu GX. Single-nucleotide polymorphism microarray-based preimplantation genetic diagnosis is likely to improve the clinical outcome for translocation carriers[J].Hum Reprod, 2013, 28 (9) : 2581-2592.
- [48]Tan YQ*, Lu GX, Lin G, Lu CF, Tan K, Gong F, Cheng DH.Cheng DH, Gong F, Tan K, Lu CF, Lin G, Lu GX, Tan YQ*. Karyotype determination and reproductive guidance for short stature women with a hidden Y chromosome fragment[J].Reproductive Biomedicine Online, 2013, 27 (1) : 89-95.
- [49]Cheng DH, Gong F, Lu CF, Li LY, Lu GX, Tan YQ.Cheng DH,Gong F,Lu CF,Li LY,Lu GX,Tan YQ*. Risk evaluation and preimplantation genetic diagnosis in an infertile man with an unbalanced translocation t(10;15) resulting in a healthy baby[J].J Assist Reprod Genet, 2012, 29 (11) : 1299-1304.
- [50]Lu GX, Li LY, Di YF, Tan YQ*, Cheng DH.Cheng DH,Tan YQ,Di YF,Li LY,Lu GX. Crypt Y chromosome fragment resulting from an X;Y translocation in a patient with premature ovarian failure[J].Fertil Steril, 2009, 92 (2) : 828.e3-6.
- [51]Lu GX, Guan XY, Hu L, Chen XM, Tan YQ*.Tan YQ, Chen XM, Hu L, Guan XY, Lu GX. Prenatal diagnosis of nonmosaic tetrasomy 9p by microdissection and FISH:case report[J].Chin Med J (Engl), 2007, 120 (14) : 1281-1283.
- [52]Lu GX, Guan XY, Gong F, Jonathan S.T.Sham, Lin G, Hu L, Tan YQ*.Tan YQ, Hu L, Lin G, Jonathan S.T.Sham, Gong F, Guan XY, Lu GX. Genetic changes in human fetuses from spontaneous abortion after in vitro fertilization detected by comparative genomic hybridization[J].Biol Reprod, 2004, 70 (2) : 495-499.
- [53]Lu GX, Tan YQ*.Tan YQ, Lu GX. Chromosomal cryptic insertion of the terminal region and its formative mechanism determined by fluorescence in situ hybridization[J].Chin Med J, 2002, 115 (7) : 1039-1042.
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