Family history as a predictor of uptake of cancer preventive procedures by women with a BRCA1 or BRCA2 mutation von Metcalfe, KA, Foulkes, WD, Kim-Sing, C, Ainsworth, P, Rosen, B, Armel, S, Poll, A, Eisen, A, Gilchrist, D, Chudley, A, Ghadirian, P, Maugard, C, Lemire, EG, Sun, P, Narod, SA

Volltext

Father-to-son transmission of an X-linked gene: A case of paternal sex chromosome heterodisomy von Ferrier, R.A., Lowry, R.B., Lemire, E.G., Stoeber, G.P., Howard, J., Parboosingh, J.S.

Volltext

Neuroimaging and Neurophysiology Studies in Carriers of Cree Leukoencephalopathy von Huntsman, R. J., Lemire, E. G., Voll, C. L., Wiebe, S., Lowry, N. J.

Volltext

An Acute Encephalopathy Accelerated by a Large Amount of Milk Consumption von Moien-Afshari, F., Mirhosseini, N.Z., Lemire, E.G., Voll, C.L.

Volltext

Hereditary nonpolyposis colon cancer von Lemire, E G

Volltext

Radiographic and prenatal ultrasound features of perinatal lethal hypophosphatasia - differentiation from osteogenesis imperfecta type II von Wiebe, S, Suchet, I, Lemire, EG

Volltext

Construction of a DNA probe and detection of Actinobacillus pleuropneumoniae by using polymerase chain reaction von Sirois, M. (Universite Laval, Quebec, Quebec, Canada), Lemire, E.G, Levesque, R.C

Volltext

Leri-Weill dyschondrosteosis: An under-recognised cause of short stature von Lemire, E G, Wiebe, S

Volltext

Peripheral Neuropathy in a Child With Cree Leukodystrophy von Huntsman, R.J., Seshia, S., Lowry, N., Lemire, E.G., Harder, S.L.

Volltext

Hallowed beginning von Lemire, Edmond G, Chudley, Albert E

Volltext

Chudley-Mccullough syndrome: Bilateral sensorineural deafness, hydrocephalus, and other structural brain abnormalities von Lemire, Edmond G., Stoeber, Gwendolyn P.

Volltext

Acute pancreatitis in a patient with glutaric acidemia type I von Lemire, Edmond G., Moroz, Stan, Pollock, Bradley, Postuma, Ray, Greenberg, Cheryl R.

Volltext

Familial neuroblastoma: Report of a kindred with later age at diagnosis von LEMIRE, E. G, CHODIRKER, B. N, WILLIAMS, G. J, SEARGEANT, L. E, ISRAELS, S. J, PHILLIPS, S. M, DE NANASSY, J. A, MARIS, J. M, YANOFSKY, R. A

Volltext

A missense mutation in the oxi-3 gene of the [mi-3] extranuclear mutant of Neurospora crassa von Lemire, E G, Nargang, F E

Volltext

1047 Congenital Analbuminemia: A Saskatchewan Case Series von Toye, J M, Baerg, K, Lemire, E G

Volltext

The mitochondrial plasmid from Neurospora intermedia strain Labelle-1b contains a long open reading frame with blocks of amino acids characteristic of reverse transcriptases and re... von PANDE, S, LEMIRE, E. G, NARGANG, F. E

Volltext

SAMS: Provisionally unique multiple congenital anomalies syndrome consisting of short stature, auditory canal atresia, mandibular hypoplasia, and skeletal abnormalities von Lemire, Edmond G., Hildes-Ripstein, G. Elske, Reed, Martin H., Chudley, Albert E.

Volltext

A familial disorder with duodenal atresia and tetralogy of Fallot von Lemire, Edmond G., Evans, Jane A., Giddins, Niels G., Harman, Christopher R., Wiseman, Nathan E., Chudley, Albert E.

Volltext

Nonspecific interstitial pneumonia and usual interstitial pneumonia with mutation in surfactant protein C in familial pulmonary fibrosis von Chibbar, Rajni, Shih, Francis, Baga, Monica, Torlakovic, Emina, Ramlall, Kumar, Skomro, Robert, Cockcroft, Donald W, Lemire, Edmond G

Volltext

Alteration of the cytochrome c oxidase subunit 2 gene in the [exn- 5] mutant of Neurospora crassa von LEMIRE, E. G, PERCY, J. A, CORREIA, J. M, CROWTHER, B. M, NARGANG, F. E

Volltext