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De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes.
Nat Genet. 2012 Jun 24;44(8):934-40. doi: 10.1038/ng.2331.
Nat Genet. 2012.
PMID: 22729224
Free PMC article.
Specific combination of compound heterozygous mutations in 17β-hydroxysteroid dehydrogenase type 4 (HSD17B4) defines a new subtype of D-bifunctional protein deficiency.
McMillan HJ, Worthylake T, Schwartzentruber J, Gottlieb CC, Lawrence SE, Mackenzie A, Beaulieu CL, Mooyer PA; FORGE Canada Consortium; Wanders RJ, Majewski J, Bulman DE, Geraghty MT, Ferdinandusse S, Boycott KM.
McMillan HJ, et al. Among authors: worthylake t.
Orphanet J Rare Dis. 2012 Nov 22;7:90. doi: 10.1186/1750-1172-7-90.
Orphanet J Rare Dis. 2012.
PMID: 23181892
Free PMC article.
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National health care improvements.
Worthylake TL.
Worthylake TL.
MGMA Connex. 2004 Jul;4(6):17-8.
MGMA Connex. 2004.
PMID: 15344609
No abstract available.
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Electronic medical risks. EMR and management responsibility.
Worthylake T, Garretson J.
Worthylake T, et al.
MGMA Connex. 2002 Jul;2(6):24-7.
MGMA Connex. 2002.
PMID: 12116621
No abstract available.
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An EDP utility could save community's health dollars.
Worthylake T, Smith RJ.
Worthylake T, et al.
Hosp Financ Manage. 1978 Feb;32(2):28-30, 33-4.
Hosp Financ Manage. 1978.
PMID: 10305307
No abstract available.
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