Chung MY - Search Results

1

DiGeorge syndrome with microdeletion of chromosome 22q11.2: report of one case.

Wang JL, Chen SJ, Chung MY, Niu DM, Lin CY, Hwang BT, Lu JH. Wang JL, et al. Among authors: chung my. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1997 Sep-Oct;38(5):385-9. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1997. PMID: 9401184

2

Prevalence and parental origin in Tetralogy of Fallot associated with chromosome 22q11 microdeletion.

Lu JH, Chung MY, Hwang B, Chien HP. Lu JH, et al. Among authors: chung my. Pediatrics. 1999 Jul;104(1 Pt 1):87-90. doi: 10.1542/peds.104.1.87. Pediatrics. 1999. PMID: 10390265

3

Chromosome 22q11 microdeletion in conotruncal heart defects: clinical presentation, parental origin and de novo mutations.

Chung MY, Lu JH, Chien HP, Hwang B. Chung MY, et al. Int J Mol Med. 2001 May;7(5):501-5. doi: 10.3892/ijmm.7.5.501. Int J Mol Med. 2001. PMID: 11295111

4

Monozygotic twins with chromosome 22q11 microdeletion and discordant phenotypes in cardiovascular patterning.

Lu JH, Chung MY, Hwang B, Chien HP. Lu JH, et al. Among authors: chung my. Pediatr Cardiol. 2001 May-Jun;22(3):260-3. doi: 10.1007/s002460010219. Pediatr Cardiol. 2001. PMID: 11343161

5

Molecular characterization of tetralogy of fallot within Digeorge critical region of the chromosome 22.

Lu JH, Chung MY, Betau H, Chien HP, Lu JK. Lu JH, et al. Among authors: chung my. Pediatr Cardiol. 2001 Jul-Aug;22(4):279-84. doi: 10.1007/s002460010230. Pediatr Cardiol. 2001. PMID: 11455393

6

Absence of mutations in human ubiquitin fusion-degradation protein gene in tetralogy of Fallot.

Chung MY, Lu JH, Weng YY, Hwang B. Chung MY, et al. J Mol Med (Berl). 2001 Jun;79(5-6):338-42. doi: 10.1007/s001090100213. J Mol Med (Berl). 2001. PMID: 11485030

7

Increased risk of attention-deficit/hyperactivity disorder associated with exposure to organophosphate pesticide in Taiwanese children.

Yu CJ, Du JC, Chiou HC, Chung MY, Yang W, Chen YS, Fuh MR, Chien LC, Hwang B, Chen ML. Yu CJ, et al. Among authors: chung my. Andrology. 2016 Jul;4(4):695-705. doi: 10.1111/andr.12183. Epub 2016 Apr 12. Andrology. 2016. PMID: 27070915 Free article.

8

Preferentially deleted chromosome region 9p21 in large hepatocellular carcinomas.

Chung MY, Wu JC, Chau GY, Lui WY, Tsay SH, Chiang H. Chung MY, et al. Int J Mol Med. 2000 May;5(5):521-4. doi: 10.3892/ijmm.5.5.521. Int J Mol Med. 2000. PMID: 10762656

9

Systematic mutation analysis of the catechol O-methyltransferase gene as a candidate gene for schizophrenia.

Chen CH, Lee YR, Chung MY, Wei FC, Koong FJ, Shaw CK, Yeh JI, Hsiao KJ. Chen CH, et al. Among authors: chung my. Am J Psychiatry. 1999 Aug;156(8):1273-5. doi: 10.1176/ajp.156.8.1273. Am J Psychiatry. 1999. PMID: 10450274

10

Adult Fanconi syndrome with proximal muscle weakness and hypophosphatemic osteomalacia: report of a case.

Lian LM, Chang YC, Yang CC, Yang JC, Kao KP, Chung MY. Lian LM, et al. Among authors: chung my. J Formos Med Assoc. 1994 Aug;93(8):709-14. J Formos Med Assoc. 1994. PMID: 7858457

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

434 results

Search Page

Filters