Lee DJ - Search Results

1

Cryptic subtelomeric deletion plus inverted duplication at chromosome 18q in a fetus: molecular delineation by multicolor banding.

Lee NC, Chang SP, Chang CS, Chen CH, Lee DJ, Lin CC, Hwu WL, Chen M. Lee NC, et al. Among authors: lee dj. Prenat Diagn. 2009 Nov;29(11):1058-60. doi: 10.1002/pd.2332. Prenat Diagn. 2009. PMID: 19629965 No abstract available.

2

Huge duplication cyst of small intestine: ultrasonographic features and prenatal aspiration.

Chen M, Ho WK, Hsieh TC, Lee CS, Hsiao CC, Chang SP, Lee DJ, Yang AD. Chen M, et al. Among authors: lee dj, lee cs. Prenat Diagn. 2006 Jan;26(1):86-8. doi: 10.1002/pd.1324. Prenat Diagn. 2006. PMID: 16374896 No abstract available.

3

Comparison of immunohistochemical and fluorescence in situ hybridization assessment for HER-2/neu status in Taiwanese breast cancer patients.

Kuo SJ, Wang BB, Chang CS, Chen TH, Yeh KT, Lee DJ, Yin PL, Chen M. Kuo SJ, et al. Among authors: lee dj. Taiwan J Obstet Gynecol. 2007 Jun;46(2):146-51. doi: 10.1016/S1028-4559(07)60008-4. Taiwan J Obstet Gynecol. 2007. PMID: 17638622 Free article.

4

Interstitial deletion 13q31 associated with normal phenotype: cytogenetic study of a family with concomitant segregation of reciprocal translocation and interstitial deletion.

Ke YY, Lee DJ, Ma GC, Lee MH, Wang BT, Chen M. Ke YY, et al. Among authors: lee dj, lee mh. J Formos Med Assoc. 2007 Jul;106(7):582-8. doi: 10.1016/S0929-6646(07)60010-2. J Formos Med Assoc. 2007. PMID: 17660149 Free article.

5

A case of restrictive dermopathy with complete chorioamniotic membrane separation caused by a novel homozygous nonsense mutation in the ZMPSTE24 gene.

Chen M, Kuo HH, Huang YC, Ke YY, Chang SP, Chen CP, Lee DJ, Lee ML, Lee MH, Chen TH, Chen CH, Lin HM, Liu CS, Ma GC. Chen M, et al. Among authors: lee dj, lee mh, lee ml. Am J Med Genet A. 2009 Jul;149A(7):1550-4. doi: 10.1002/ajmg.a.32768. Am J Med Genet A. 2009. PMID: 19504603 No abstract available.

6

De novo triple segmental aneuploid of 1p, 1q, and 4q in a girl with hypertrophic cardiomyopathy, muscle hypotonia, and multiple congenital anomalies.

Ma GC, Ke YY, Lee ML, Tsao LY, Lee DJ, Yang CW, Kuo SJ, Chiu HY, Chen M. Ma GC, et al. Among authors: lee dj, lee ml. Am J Med Genet A. 2010 Mar;152A(3):784-8. doi: 10.1002/ajmg.a.33157. Am J Med Genet A. 2010. PMID: 20140964 No abstract available.

7

Complex rearrangements between chromosomes 6, 10, and 11 with multiple deletions at breakpoints.

Lee NC, Chen M, Ma GC, Lee DJ, Wang TJ, Ke YY, Chien YH, Hwu WL. Lee NC, et al. Among authors: lee dj. Am J Med Genet A. 2010 Sep;152A(9):2327-34. doi: 10.1002/ajmg.a.33581. Am J Med Genet A. 2010. PMID: 20684005

8

Molecular delineation of the Y-borne Sry gene in the Formosan pangolin (Manis pentadactyla pentadactyla) and its phylogenetic implications for Pholidota in extant mammals.

Yu HT, Ma GC, Lee DJ, Chin SC, Tsao HS, Wu SH, Shih SY, Chen M. Yu HT, et al. Among authors: lee dj. Theriogenology. 2011 Jan 1;75(1):55-64. doi: 10.1016/j.theriogenology.2010.07.010. Epub 2010 Aug 23. Theriogenology. 2011. PMID: 20739052

9

Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3→pter) and partial monosomy 13q (13q33.3→qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly.

Chen CP, Chen M, Su YN, Tsai FJ, Chern SR, Hsu CY, Wu PC, Town DD, Lee DJ, Ma GC, Wang W. Chen CP, et al. Among authors: lee dj. Taiwan J Obstet Gynecol. 2010 Sep;49(3):320-6. doi: 10.1016/S1028-4559(10)60068-X. Taiwan J Obstet Gynecol. 2010. PMID: 21056318 Free article.

10

A compound heterozygous GNPTAB mutation causes mucolipidosis II with marked hair color change in a Han Chinese baby.

Ma GC, Ke YY, Chang SP, Lee DJ, Chen M. Ma GC, et al. Among authors: lee dj. Am J Med Genet A. 2011 Apr;155A(4):931-4. doi: 10.1002/ajmg.a.33834. Epub 2011 Mar 17. Am J Med Genet A. 2011. PMID: 21416587 No abstract available.

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