Huang SZ - Search Results

1

Sexing bovine embryos using PCR amplification of bovine SRY sequence.

Zeng YT, Zhang ML, Chen MJ, Zhou XD, Huang Y, Ren ZR, Huang SZ, Hu MX, Wu XQ, Gao JM, et al. Zeng YT, et al. Among authors: huang sz, huang y. Sci China B. 1994 Feb;37(2):170-6. Sci China B. 1994. PMID: 8068189

2

Study of the RNA splicing defect in the common Chinese beta-thalassemia gene, IVS-II nt. 654 C-->T by using mRNA/PCR.

Huang SZ, Ren ZR, Zeng YT, Zeng FY, Rodgers GP, Schecter AN. Huang SZ, et al. Sci China B. 1992 Oct;35(10):1232-7. Sci China B. 1992. PMID: 1285849

3

Detection of molecular deletions in the Chinese DMD patients using two amplified dystrophin sequences.

Zeng YT, Chen MJ, Ren ZR, Huang Y, Qiu XK, Huang SZ. Zeng YT, et al. Among authors: huang sz, huang y. Biochem Med Metab Biol. 1992 Apr;47(2):195-7. doi: 10.1016/0885-4505(92)90024-s. Biochem Med Metab Biol. 1992. PMID: 1515177

4

Diagnosis of thalassemia using cDNA amplification of circulating erythroid cell mRNA with the polymerase chain reaction.

Huang SZ, Rodgers GP, Zeng FY, Zeng YT, Schechter AN. Huang SZ, et al. Blood. 1992 Jun 15;79(12):3397. Blood. 1992. PMID: 1627791 Free article. No abstract available.

5

Identification of three novel missense PKU mutations among Chinese.

Li J, Eisensmith RC, Wang T, Lo WH, Huang SZ, Zeng YT, Yuan LF, Liu SR, Woo SL. Li J, et al. Among authors: huang sz. Genomics. 1992 Jul;13(3):894-5. doi: 10.1016/0888-7543(92)90180-z. Genomics. 1992. PMID: 1639423

6

Analysis of RFLPs and DNA deletions in the Chinese Duchenne muscular dystrophy gene.

Zeng YT, Chen MJ, Ren ZR, Qui XK, Huang SZ. Zeng YT, et al. Among authors: huang sz. J Med Genet. 1991 Mar;28(3):167-70. doi: 10.1136/jmg.28.3.167. J Med Genet. 1991. PMID: 1675685 Free PMC article.

7

Diagnosis of thalassemia using cDNA amplification of circulating erythroid cell mRNA with the polymerase chain reaction.

Huang SZ, Rodgers GP, Zeng FY, Zeng YT, Schechter AN. Huang SZ, et al. Blood. 1991 Nov 1;78(9):2433-7. Blood. 1991. PMID: 1932755 Free article.

8

Application of a new DNA sequence polymorphism as a genetic marker in prenatal diagnosis of phenylketonuria.

Huang SZ, Ren ZR, Zeng YT. Huang SZ, et al. J Med Genet. 1990 Jan;27(1):65-6. doi: 10.1136/jmg.27.1.65. J Med Genet. 1990. PMID: 1968515 Free PMC article. No abstract available.

9

Prenatal detection of an Arg----Ter mutation at codon 111 of the PAH gene using DNA amplification.

Huang SZ, Zhou XD, Ren ZR, Zeng YT, Woo SL. Huang SZ, et al. Prenat Diagn. 1990 May;10(5):289-93. doi: 10.1002/pd.1970100503. Prenat Diagn. 1990. PMID: 1975096

10

PAH 399 GTA (Val)----GTT(Val), a new silent mutation found in the Chinese.

Huang SZ, Ren ZR, Zeng YT, Woo SL. Huang SZ, et al. Hum Genet. 1991 Jan;86(3):305-6. doi: 10.1007/BF00202416. Hum Genet. 1991. PMID: 1997387

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