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Results: 1-17 |
Results: 17
Second-trimester molecular diagnosis of a heterozygous 742C -> T (R248C) mutation in the FGFR3 gene in a thanatophoric dysplasia variant following suspicious ultrasound findings
Authors: Chen, CP Chern, SR Wang, W Wang, TY
Citation: Cp. Chen et al., Second-trimester molecular diagnosis of a heterozygous 742C -> T (R248C) mutation in the FGFR3 gene in a thanatophoric dysplasia variant following suspicious ultrasound findings, ULTRASOUN O, 17(3), 2001, pp. 272-273
Prenatal diagnosis of partial monosomy 18p(18p11.2 -> pter) and trisomy 21q(21q22.3 -> qter) with alobar holoprosencephaly and premaxillary agenesis
Authors: Chen, CP Chern, SR Wang, W Lee, CC Chen, WL Chen, LF Chang, TY Tzen, CY
Citation: Cp. Chen et al., Prenatal diagnosis of partial monosomy 18p(18p11.2 -> pter) and trisomy 21q(21q22.3 -> qter) with alobar holoprosencephaly and premaxillary agenesis, PRENAT DIAG, 21(5), 2001, pp. 346-350
Prenatal diagnosis of de novo distal 11q deletion associated with sonographic findings of unilateral duplex renal system, pyelectasis and orofacial clefts
Authors: Chen, CP Chern, SR Tzen, CY Lee, MS Pan, CW Chang, TY Wang, W
Citation: Cp. Chen et al., Prenatal diagnosis of de novo distal 11q deletion associated with sonographic findings of unilateral duplex renal system, pyelectasis and orofacial clefts, PRENAT DIAG, 21(4), 2001, pp. 317-320
Prenatal diagnosis and genetic analysis of type I and type II thanatophoric dysplasia
Authors: Chen, CP Chern, SR Shih, JC Wang, WS Yeh, LF Chang, TY Tzen, CY
Citation: Cp. Chen et al., Prenatal diagnosis and genetic analysis of type I and type II thanatophoric dysplasia, PRENAT DIAG, 21(2), 2001, pp. 89-95
Prenatal diagnosis of mosaic ring chromosome 13 with anencephaly
Authors: Chen, CP Chern, SR Lee, CC Chen, WL Wang, WS
Citation: Cp. Chen et al., Prenatal diagnosis of mosaic ring chromosome 13 with anencephaly, PRENAT DIAG, 21(2), 2001, pp. 102-105
Multiple globules in a cystic ovarian teratoma
Authors: Chen, CP Chern, SR Wang, WS Wang, KL Wang, TY
Citation: Cp. Chen et al., Multiple globules in a cystic ovarian teratoma, FERT STERIL, 75(3), 2001, pp. 618-619
Fetal DNA analyzed in plasma from a mother's three consecutive pregnanciesto detect paternally inherited aneuploidy
Authors: Chen, CP Chern, SR Wang, W
Citation: Cp. Chen et al., Fetal DNA analyzed in plasma from a mother's three consecutive pregnanciesto detect paternally inherited aneuploidy, CLIN CHEM, 47(5), 2001, pp. 937-939
Rapid determination of zygosity and common aneuploidies from amniotic fluid cells using quantitative fluorescent polymerase chain reaction following genetic amniocentesis in multiple pregnancies
Authors: Chen, CP Chern, SR Wang, W
Citation: Cp. Chen et al., Rapid determination of zygosity and common aneuploidies from amniotic fluid cells using quantitative fluorescent polymerase chain reaction following genetic amniocentesis in multiple pregnancies, HUM REPR, 15(4), 2000, pp. 929-934
Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18
Authors: Chen, CP Chern, SR Yeh, LF Chen, WL Chen, LF Wang, W
Citation: Cp. Chen et al., Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18, PRENAT DIAG, 20(9), 2000, pp. 750-753
Prenatal diagnosis and genetic analysis of X chromosome polysomy 49,XXXXY
Authors: Chen, CP Chern, SR Chang, CL Lee, CC Chen, WL Chen, LF Wang, W
Citation: Cp. Chen et al., Prenatal diagnosis and genetic analysis of X chromosome polysomy 49,XXXXY, PRENAT DIAG, 20(9), 2000, pp. 754-757
Prenatal diagnosis of inherited satellited non-acrocentric chromosomes
Authors: Chen, CP Devriendt, K Chern, SR Lee, CC Wang, WS Lin, SP
Citation: Cp. Chen et al., Prenatal diagnosis of inherited satellited non-acrocentric chromosomes, PRENAT DIAG, 20(5), 2000, pp. 384-389
Fetal DNA in maternal plasma: the prenatal detection of a paternally inherited fetal aneuploidy
Authors: Chen, CP Chern, SR Wang, WS
Citation: Cp. Chen et al., Fetal DNA in maternal plasma: the prenatal detection of a paternally inherited fetal aneuploidy, PRENAT DIAG, 20(4), 2000, pp. 355-357
Molecular prenatal diagnosis of thalassemia in Taiwan
Authors: Chern, SR Chen, CP
Citation: Sr. Chern et Cp. Chen, Molecular prenatal diagnosis of thalassemia in Taiwan, INT J GYN O, 69(2), 2000, pp. 103-106
Hamartoma in a pubertal patient with complete androgen insensitivity syndrome and R(831)X mutation of the androgen receptor gene
Authors: Chen, CP Chern, SR Chen, BF Wang, W Hwu, YM
Citation: Cp. Chen et al., Hamartoma in a pubertal patient with complete androgen insensitivity syndrome and R(831)X mutation of the androgen receptor gene, FERT STERIL, 74(1), 2000, pp. 182-183
Androgen receptor gene mutations in 46,XY females with germ cell tumours
Authors: Chen, CP Chern, SR Wang, TY Wang, W Wang, KL Jeng, CJ
Citation: Cp. Chen et al., Androgen receptor gene mutations in 46,XY females with germ cell tumours, HUM REPR, 14(3), 1999, pp. 664-670
Bilateral renal agenesis and fetal ascites in association with partial trisomy 13 and partial trisomy 16 due to a 3 : 1 segregation of maternal reciprocal translocation t(13;16)(q12.3; p13.2)
Authors: Chen, CP Chern, SR Lee, CC Town, DD Chen, WL Wang, WS
Citation: Cp. Chen et al., Bilateral renal agenesis and fetal ascites in association with partial trisomy 13 and partial trisomy 16 due to a 3 : 1 segregation of maternal reciprocal translocation t(13;16)(q12.3; p13.2), PRENAT DIAG, 19(8), 1999, pp. 783-786
Exceptions to nature demand a higher level of documentation - Reply
Authors: Chen, CP Hwu, YM Chen, CP Chern, SR Wang, W Wang, TY
Citation: Cp. Chen et al., Exceptions to nature demand a higher level of documentation - Reply, FERT STERIL, 72(6), 1999, pp. 1151-1152
Risultati: 1-17 |