Hsieh LJ - Search Results

1

Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy 5q.

Chen CP, Lin SP, Lin CC, Chen YJ, Chern SR, Li YC, Hsieh LJ, Lee CC, Pan CW, Wang W. Chen CP, et al. Among authors: hsieh lj. Am J Med Genet A. 2006 Jul 15;140(14):1594-600. doi: 10.1002/ajmg.a.31329. Am J Med Genet A. 2006. PMID: 16770806 Review.

2

Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).

Chen CP, Chern SR, Lin CC, Wang TH, Li YC, Hsieh LJ, Lee CC, Hua HM, Wang W. Chen CP, et al. Among authors: hsieh lj. Prenat Diagn. 2006 Apr;26(4):313-20. doi: 10.1002/pd.1399. Prenat Diagn. 2006. PMID: 16506269 Review.

3

Primary ovarian failure in a mentally retarded woman with a de novo unbalanced X;autosome translocation.

Chen CP, Lin CC, Li YC, Hsieh LJ, Lee CC, Wang W. Chen CP, et al. Among authors: hsieh lj. Fertil Steril. 2006 Nov;86(5):1514.e1-2. doi: 10.1016/j.fertnstert.2006.02.127. Fertil Steril. 2006. PMID: 17070202 Free article.

4

Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter).

Chen CP, Lin SP, Lin CC, Li YC, Chern SR, Chen WM, Lee CC, Hsieh LJ, Wang W. Chen CP, et al. Among authors: hsieh lj. Prenat Diagn. 2005 Feb;25(2):112-8. doi: 10.1002/pd.1083. Prenat Diagn. 2005. PMID: 15712324 Review.

5

A paternally derived inverted duplication of distal 14q with a terminal 14q deletion.

Chen CP, Chern SR, Lin SP, Lin CC, Li YC, Wang TH, Lee CC, Pan CW, Hsieh LJ, Wang W. Chen CP, et al. Among authors: hsieh lj. Am J Med Genet A. 2005 Dec 1;139A(2):146-50. doi: 10.1002/ajmg.a.30997. Am J Med Genet A. 2005. PMID: 16278896

6

Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.

Chen CP, Chern SR, Lee CC, Lin CC, Li YC, Hsieh LJ, Chen WL, Wang W. Chen CP, et al. Among authors: hsieh lj. Prenat Diagn. 2006 Feb;26(2):138-46. doi: 10.1002/pd.1369. Prenat Diagn. 2006. PMID: 16470734 Review.

7

Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.

Lin CC, Hsieh YY, Wang CH, Li YC, Hsieh LJ, Lee CC, Tsai CH, Tsai FJ. Lin CC, et al. Among authors: hsieh yy, hsieh lj. Prenat Diagn. 2006 Oct;26(10):898-902. doi: 10.1002/pd.1520. Prenat Diagn. 2006. PMID: 16915592

8

Prenatal diagnosis of partial trisomy 3p (3p21-->pter) and partial monosomy 11q (11q23-->qter) associated with abnormal sonographic findings of holoprosencephaly, orofacial clefts, pyelectasis and a unilateral duplex renal system.

Chen CP, Wang TH, Lin CC, Tsai FJ, Hsieh LJ, Wang W. Chen CP, et al. Among authors: hsieh lj. J Formos Med Assoc. 2008 Oct;107(10):822-6. doi: 10.1016/S0929-6646(08)60197-7. J Formos Med Assoc. 2008. PMID: 18926951 Free article.

9

Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter).

Chen CP, Lin SP, Lin CC, Li YC, Hsieh LJ, Chern SR, Lee CC, Chen YJ, Wang W. Chen CP, et al. Among authors: hsieh lj. Prenat Diagn. 2005 Dec;25(12):1170-2. doi: 10.1002/pd.1300. Prenat Diagn. 2005. PMID: 16315335 No abstract available.

10

Molecular cytogenetic analysis of de novo dup(5)(q33.1q31.1) associated with abnormal perinatal findings.

Chen CP, Lin SP, Chern SR, Lin CC, Li YC, Lee CC, Hsieh LJ, Chen WL, Wang W. Chen CP, et al. Among authors: hsieh lj. Prenat Diagn. 2006 Feb;26(2):181-3. doi: 10.1002/pd.1365. Prenat Diagn. 2006. PMID: 16470511 Review. No abstract available.

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