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K Y Loke

Showing results (1-10 of 29) with videos related to

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The Journal of the Singapore Paediatric Society|January 1, 1991
Congenital adrenal hyperplasiaK Y Loke
The Journal of the Singapore Paediatric Society|January 1, 1991
Cockayne syndrome--a case report, and a review of the premature aging syndromes in paediatricsK Y Loke
Annals of the Academy of Medicine, Singapore|March 11, 2003
The perils of pubertyK Y Loke, R M Viner
Annals of the Academy of Medicine, Singapore|September 8, 2000
The molecular pathogenesis of obesity: an unfinished jigsaw puzzleY S Lee, K Y Loke
Journal of Clinical Pathology|June 29, 2006
Isolated haploinsufficiency of exon 1 of the SHOX gene in a patient with idiopathic short statureY-M Tan, K-Y Loke
Singapore Medical Journal|April 18, 2008
Gonadal mosaicism 45,X/46,X,psu dic(Y)(q11.2) resulting in a Turner phenotype with mixed gonadal dysgenesisL A Gole, J Lim, J A Crolla, et al.
Journal of Tropical Pediatrics|May 5, 2001
Type II Gaucher disease: compound heterozygote with RecNciI and L444P mutationsY S Lee, L K Poh, H Ida, et al.
Pediatric Nephrology (Berlin, Germany)|April 16, 1998
Subclinical activation of lupus nephritis by recombinant human growth hormoneH K Yap, K Y Loke, B Murugasu, et al.
Journal of Paediatrics and Child Health|May 29, 2002
Maternal thyrotoxicosis causing central hypothyroidism in infantsY S Lee, K Y Loke, S C Y Ng, et al.
Hormone Research|October 13, 2001
Molecular analysis of CYP-21 mutations for congenital adrenal hyperplasia in SingaporeK Y Loke, Y S Lee, W W Lee, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
The Journal of the Singapore Paediatric Society|January 1, 1991
Congenital adrenal hyperplasiaK Y Loke
The Journal of the Singapore Paediatric Society|January 1, 1991
Cockayne syndrome--a case report, and a review of the premature aging syndromes in paediatricsK Y Loke
Annals of the Academy of Medicine, Singapore|March 11, 2003
The perils of pubertyK Y Loke, R M Viner
Annals of the Academy of Medicine, Singapore|September 8, 2000
The molecular pathogenesis of obesity: an unfinished jigsaw puzzleY S Lee, K Y Loke
Journal of Clinical Pathology|June 29, 2006
Isolated haploinsufficiency of exon 1 of the SHOX gene in a patient with idiopathic short statureY-M Tan, K-Y Loke
Singapore Medical Journal|April 18, 2008
Gonadal mosaicism 45,X/46,X,psu dic(Y)(q11.2) resulting in a Turner phenotype with mixed gonadal dysgenesisL A Gole, J Lim, J A Crolla, et al.
Journal of Tropical Pediatrics|May 5, 2001
Type II Gaucher disease: compound heterozygote with RecNciI and L444P mutationsY S Lee, L K Poh, H Ida, et al.
Pediatric Nephrology (Berlin, Germany)|April 16, 1998
Subclinical activation of lupus nephritis by recombinant human growth hormoneH K Yap, K Y Loke, B Murugasu, et al.
Journal of Paediatrics and Child Health|May 29, 2002
Maternal thyrotoxicosis causing central hypothyroidism in infantsY S Lee, K Y Loke, S C Y Ng, et al.
Hormone Research|October 13, 2001
Molecular analysis of CYP-21 mutations for congenital adrenal hyperplasia in SingaporeK Y Loke, Y S Lee, W W Lee, et al.
Pageof 3