Hwang B - Search Results

1

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: hwang b. Pediatr Cardiol. 2001 May-Jun;22(3):260-3. doi: 10.1007/s002460010219. Pediatr Cardiol. 2001. PMID: 11343161

2

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: hwang bt. 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

3

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: hwang b. Pediatrics. 1999 Jul;104(1 Pt 1):87-90. doi: 10.1542/peds.104.1.87. Pediatrics. 1999. PMID: 10390265

4

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. Among authors: hwang b. Int J Mol Med. 2001 May;7(5):501-5. doi: 10.3892/ijmm.7.5.501. Int J Mol Med. 2001. PMID: 11295111

5

Tracheal agenesis with multiple congenital anomalies: a case report.

Wang CM, Chen SJ, Lu JH, Hwang BT. Wang CM, et al. Among authors: hwang bt. Zhonghua Yi Xue Za Zhi (Taipei). 1998 Jan;61(1):48-52. Zhonghua Yi Xue Za Zhi (Taipei). 1998. PMID: 9509693

6

A clinical observation of term infants with critical cardiovascular disorders.

Lee BC, Hwang B, Hsieng JH, Lu JH, Meng CC. Lee BC, et al. Among authors: hwang b. Zhonghua Yi Xue Za Zhi (Taipei). 1996 Aug;58(2):103-7. Zhonghua Yi Xue Za Zhi (Taipei). 1996. PMID: 8915112

7

Detachment of balloon in an infant: a rare complication of balloon pulmonary valvuloplasty.

Hwang B, Lee BC, Lu JH, Meng CC. Hwang B, et al. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1996 Nov-Dec;37(6):451-4. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1996. PMID: 9074284

8

Treatment of pulmonary atresia with intact ventricular septum in early infancy.

Hsieh WH, Hwang B, Lu JH, Lee PC, Fu YC, Shing HP, Meng CC. Hsieh WH, et al. Among authors: hwang b. Zhonghua Yi Xue Za Zhi (Taipei). 1999 Sep;62(9):626-32. Zhonghua Yi Xue Za Zhi (Taipei). 1999. PMID: 10502854

9

Influence of ventricular septal defect type on surgical results in children with tetralogy of Fallot.

Fu YC, Hwang B, Weng ZC, Lu JH, Chi CS, Meng CC. Fu YC, et al. Among authors: hwang b. Zhonghua Yi Xue Za Zhi (Taipei). 2000 Nov;63(11):792-7. Zhonghua Yi Xue Za Zhi (Taipei). 2000. PMID: 11155754

10

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. Among authors: hwang b. J Mol Med (Berl). 2001 Jun;79(5-6):338-42. doi: 10.1007/s001090100213. J Mol Med (Berl). 2001. PMID: 11485030

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