Lo IF - 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: lo if. 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

Williams-Beuren syndrome in the Hong Kong Chinese population: retrospective study.

Yau EK, Lo IF, Lam ST. Yau EK, et al. Among authors: lo if. Hong Kong Med J. 2004 Feb;10(1):22-7. Hong Kong Med J. 2004. PMID: 14967851 Free article.

3

Dentatorubral-pallidoluysian atrophy in two Chinese families in Hong Kong.

Yam WK, Wu NS, Lo IF, Ko CH, Yeung WL, Lam ST. Yam WK, et al. Among authors: lo if. Hong Kong Med J. 2004 Feb;10(1):53-6. Hong Kong Med J. 2004. PMID: 14967857 Free article.

4

XX-agonadism in a fetus with multiple congenital anomalies.

Woo HH, Lo IF, Tse HY, Lam ST, Tang CH. Woo HH, et al. Among authors: lo if. Am J Med Genet A. 2004 Apr 1;126A(1):104-5. doi: 10.1002/ajmg.a.20554. Am J Med Genet A. 2004. PMID: 15039981 Review.

5

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: lo if. Hong Kong Med J. 2005 Aug;11(4):243-50. Hong Kong Med J. 2005. PMID: 16085940 Free article.

6

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. Among authors: lo if. Chin Med J (Engl). 2005 Sep 20;118(18):1499-506. Chin Med J (Engl). 2005. PMID: 16232326

7

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: lo if. 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

8

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: lo sy, lo if. Prenat Diagn. 2006 Nov;26(11):1018-20. doi: 10.1002/pd.1547. Prenat Diagn. 2006. PMID: 16941720

9

Severe neonatal manifestations of Costello syndrome.

Lo IF, Brewer C, Shannon N, Shorto J, Tang B, Black G, Soo MT, Ng DK, Lam ST, Kerr B. Lo IF, et al. J Med Genet. 2008 Mar;45(3):167-71. doi: 10.1136/jmg.2007.054411. Epub 2007 Nov 26. J Med Genet. 2008. PMID: 18039947

10

Ambiguous genitalia, impaired steroidogenesis, and Antley-Bixler syndrome in a patient with P450 oxidoreductase deficiency.

But WM, Lo IF, Shek CC, Tse WY, Lam ST. But WM, et al. Among authors: lo if. Hong Kong Med J. 2010 Feb;16(1):59-62. Hong Kong Med J. 2010. PMID: 20124576 Free article.

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