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McInnes, Brenda
26  results:
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1

P580: Care4Rare Canada: Application of a multi-omics protoc..:

Soubry, Elisabeth ; Hartley, Taila ; Ackers, Meryl...
Genetics in Medicine Open.  2 (2024)  - p. 101486 , 2024
Link: https://doi.org/10.1016/..
 
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2

(Un)standardized testing: the diagnostic odyssey of childre..:

Michaels-Igbokwe, Christine ; McInnes, Brenda ; MacDonald, Karen V....
Genetics in Medicine.  23 (2021)  2 - p. 272-279 , 2021
Link: https://doi.org/10.1038/..
 
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3

Automated syndrome diagnosis by three-dimensional facial im..:

Hallgrímsson, Benedikt ; Aponte, J. David ; Katz, David C....
Genetics in Medicine.  22 (2020)  10 - p. 1682-1693 , 2020
Link: https://doi.org/10.1038/..
 
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4

The value of diagnostic testing for parents of children wit..:

Marshall, Deborah A. ; MacDonald, Karen V. ; Heidenreich, Sebastian...
Genetics in Medicine.  21 (2019)  12 - p. 2798-2806 , 2019
Link: https://doi.org/10.1038/..
 
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5

Correction: The value of diagnostic testing for parents of ..:

Marshall, Deborah A. ; MacDonald, Karen V. ; Heidenreich, Sebastian...
Genetics in Medicine.  21 (2019)  11 - p. 2662 , 2019
Link: https://doi.org/10.1038/..
 
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6

Clinical and genetic heterogeneity in Dubowitz syndrome: Im..:

Innes, A. Micheil ; McInnes, Brenda L. ; Dyment, David A.
American Journal of Medical Genetics Part C: Seminars in Medical Genetics.  178 (2018)  4 - p. 387-397 , 2018
Link: https://doi.org/10.1002/..
 
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7

Longer Term Survival of a Child With Autosomal Recessive Cu..:

Sawyer, Sarah L. ; Dicke, Frank ; Kirton, Adam...
American Journal of Medical Genetics Part A.  161 (2013)  5 - p. 1148-1153 , 2013
Link: https://doi.org/10.1002/..
 
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8

Frontometaphyseal dysplasia: Mutations in FLNA and phenotyp..:

Robertson, Stephen P. ; Jenkins, Zandra A. ; Morgan, Timothy...
American Journal of Medical Genetics Part A.  140A (2006)  24 - p. 2840-2840 , 2006
Link: https://doi.org/10.1002/..
 
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9

Frontometaphyseal dysplasia: Mutations in FLNA and phenotyp..:

Robertson, Stephen P. ; Jenkins, Zandra A. ; Morgan, Timothy...
American Journal of Medical Genetics Part A.  140A (2006)  16 - p. 1726-1736 , 2006
Link: https://doi.org/10.1002/..
 
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10

Analysis of aneuploidy for chromosomes 13, 21, X and Y by m..:

Martin, Renée H. ; McInnes, Brenda ; Rademaker, A.W.
Zygote.  7 (1999)  2 - p. 131-134 , 1999
Link: https://doi.org/10.1017/..
 
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11

Automated syndrome diagnosis by three-dimensional facial im..:

Hallgrímsson, Benedikt ; Aponte, J David ; Katz, David C...
qt0tv3r47x.  , 2020
Link: https://escholarship.org..
 
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12

Automated syndrome diagnosis by three-dimensional facial im..:

Hallgrímsson, Benedikt ; Aponte, J. David ; Katz, David C...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521994/.  , 2020
Link: http://www.ncbi.nlm.nih...
 
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13

Alternative genomic diagnoses for individuals with a clinic..:

Dyment, David A ; O'Donnell-Luria, Anne ; Agrawal, Pankaj B...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8197629/.  , 2020
Link: http://www.ncbi.nlm.nih...
 
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14

Alternative genomic diagnoses for individuals with a clinic..:

Dyment, D. A. (David A.) ; O'Donnell-Luria, A. (Anne) ; Agrawal, P. B. (Pankaj B.)... , 2021
Link: http://urn.fi/urn:nbn:fi..
 
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15

Contribution ofStroketo the Cochrane Stroke Group Trials Re..:

Thomas, Brenda ; McInnes, Alison ; Sandercock, Peter
Stroke.  34 (2003)  2 - p. 374-378 , 2003
Link: https://doi.org/10.1161/..
 
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