L. Armstrong, MD, BSc

Clinical Assistant Professor
Department of Medical Genetics
Children's & Women's Health Centre of B.C.
4500 Oak Street, Room C234
Vancouver, B.C. V6H 3N1

Fax: (604) 875-2376
Email: llarmstrong@cw.bc.ca

Research Interests: The phenotypic and genotypic characterization of rare syndromes.

Selected Publications:

Armstrong L, McGowan-Jordan J, Brierley K, Allanson JE.  De novo dup(X)(q22.3q26) in a girl with evidence that functional disomy of X material is the cause of her abnormal phenotype. Am J Med Genet. 2003 Jan 1;116A(1):71-6.

Armstrong L, Jimenez C, Hunter AG.  A boy with developmental delay, malformations, and evidence of a connective tissue disorder: possibly a new type of cutis laxa. Am J Med Genet. 2003 May 15;119A(1):57-62.

Armstrong L, Clarke JT. Report of a new case of "genitopatellar" syndrome which challenges the importance of absent patellae as a defining feature. J Med Genet. 2002 Dec;39(12):933-4.