Tong TM - Search Results

1

Triple-A syndrome--the first Chinese patient with novel mutations in the AAAS gene.

Lam YY, Lo IF, Shek CC, Tong TM, Ng DK, Tong TF, Choi MS, Lam ST, Ho CS. Lam YY, et al. Among authors: tong tf, tong tm. J Pediatr Endocrinol Metab. 2006 May;19(5):765-70. doi: 10.1515/jpem.2006.19.5.765. J Pediatr Endocrinol Metab. 2006. PMID: 16789645

2

Spectrum of NSD1 gene mutations in southern Chinese patients with Sotos syndrome.

Tong TM, Hau EW, Lo IF, Chan DH, Lam ST. Tong TM, et al. Chin Med J (Engl). 2005 Sep 20;118(18):1499-506. Chin Med J (Engl). 2005. PMID: 16232326

3

Detecting exon deletions and duplications of the DMD gene using Multiplex Ligation-dependent Probe Amplification (MLPA).

Lai KK, Lo IF, Tong TM, Cheng LY, Lam ST. Lai KK, et al. Among authors: tong tm. Clin Biochem. 2006 Apr;39(4):367-72. doi: 10.1016/j.clinbiochem.2005.11.019. Epub 2006 Jan 17. Clin Biochem. 2006. PMID: 16413013

4

Metaphyseal chondrodysplasia McKusick type in a Chinese fetus, caused by novel compound heterozygosity 64T> A and 79G >T in RMRPgene.

Lam AC, Chan DH, Tong TM, Tang MH, Lo SY, Lo IF, Lam ST. Lam AC, et al. Among authors: tong tm. Prenat Diagn. 2006 Nov;26(11):1018-20. doi: 10.1002/pd.1547. Prenat Diagn. 2006. PMID: 16941720

5

Congenital fibrosis of extraocular muscle type 1A due to KIF21A mutation: first case report from Hong Kong.

Luk HM, Lo IF, Lai CW, Ma LC, Tong TM, Chan DH, Lam ST. Luk HM, et al. Among authors: tong tm. Hong Kong Med J. 2013 Apr;19(2):182-5. Hong Kong Med J. 2013. PMID: 23535681 Free article.

6

A young woman with mucocutaneous pigmentation and intestinal polyps.

Luk HM, Lo IF, Yu KM, Tong TM, Lam ST. Luk HM, et al. Among authors: tong tm. Hong Kong Med J. 2013 Jun;19(3):276.e3-4. doi: 10.12809/hkmj133753. Hong Kong Med J. 2013. PMID: 23732439 Free article. No abstract available.

7

Chromosomal abnormalities and FMR1 gene premutation in Chinese women with premature menopause.

Lo TK, Lo IF, Chan WK, Tong TM, Lam ST. Lo TK, et al. Among authors: tong tm. Hong Kong Med J. 2005 Aug;11(4):243-50. Hong Kong Med J. 2005. PMID: 16085940 Free article.

8

The nail points to the diagnosis. Fong disease or hereditary osteo-onychodysplasia.

Tong SY, Luk HM, Tong TM, Lo IF. Tong SY, et al. Among authors: tong tm. Hong Kong Med J. 2015 Dec;21(6):573.e3-5. doi: 10.12809/hkmj154728. Hong Kong Med J. 2015. PMID: 26634378 Free article. No abstract available.

9

Oculopharyngeal muscular dystrophy: underdiagnosed disease in Hong Kong.

Luk HM, Lo IF, Fu KH, Lui CH, Tong TM, Chan DH, Lam ST. Luk HM, et al. Among authors: tong tm. Hong Kong Med J. 2013 Dec;19(6):556-9. doi: 10.12809/hkmj133739. Hong Kong Med J. 2013. PMID: 24310666 Free article.

10

Genetic landscape of RASopathies in Chinese: Three decades' experience in Hong Kong.

Yu KPT, Luk HM, Leung GKC, Mak CCY, Cheng SSW, Hau EWL, Chan DKH, Lam STS, Tong TMF, Chung BHY, Lo IFM. Yu KPT, et al. Am J Med Genet C Semin Med Genet. 2019 Jun;181(2):208-217. doi: 10.1002/ajmg.c.31692. Epub 2019 Mar 21. Am J Med Genet C Semin Med Genet. 2019. PMID: 30896080

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

41 results

Search Page

Filters