M.D. Speevak: search on Z-Library

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1

A novel complex mutation in MSH2 contributes to both Muir-Torre and Lynch Syndrome

Perera, Sheron, Ramyar, Lily, Mitri, Angie, Pollett, Aaron, Gallinger, Steven, Speevak, Marsha D, Aronson, Melyssa, Bapat, Bharati

Journal:

Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 269 KB

english, 2010

2

Multiple Attributes Sampling Acceptance Plans Involving Destructive Testing

Speevak, T., Yu, A. K.

Journal:

Year:

1987

Language:

english

File:

PDF, 554 KB

english, 1987

3

Multiple Attributes Sampling Acceptance Plans Involving Destructive Testing

Speevak, T., Yu, A. K.

Journal:

Year:

1987

Language:

english

File:

PDF, 421 KB

english, 1987

4

CCMG practice guideline: laboratory guidelines for next-generation sequencing

Hume, Stacey, Nelson, Tanya N, Speevak, Marsha, McCready, Elizabeth, Agatep, Ron, Feilotter, Harriet, Parboosingh, Jillian, Stavropoulos, Dimitri J, Taylor, Sherryl, Stockley, Tracy L

Journal:

Journal of Medical Genetics

Year:

2019

File:

PDF, 286 KB

2019

5

Molecular and cytogenetic characterization of a prenatally ascertained de novo (X;Y) translocation

M. Speevak, S.A. Farrell, D. Chadwick

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 49 KB

english, 2001

6

Mosaic r(13) in an infant with aprosencephaly

Claire L. Goldsmith, George F. Tawagi, Blair F. Carpenter, Marsha D. Speevak, Alasdair G. W. Hunter

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 350 KB

english, 1993

7

Molecular characterization of an inherited ring (19) demonstrating ring opening

Marsha D. Speevak, Carolin Smart, Lianne Unwin, Morag Bell, Sandra A. Farrell

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 126 KB

english, 2003

8

Non-syndromic language delay in a child with disruption in the Protocadherin11X/Y gene pair

Marsha D. Speevak, Sandra A. Farrell

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2011

Language:

english

File:

PDF, 288 KB

english, 2011

9

Recombinant Down syndrome: a case report and literature review

SJ Lazzaro, MD Speevak, SA Farrell

Journal:

Clinical Genetics

Year:

2001

Language:

english

File:

PDF, 77 KB

english, 2001

10

Pure partial trisomy of 2q22-q23 secondary to a paternally inherited direct insertion: a rare duplication

S.A. Farrell, A. Sajoo, D. Maybury, M.D. Speevak

Journal:

Clinical Genetics

Year:

2003

Language:

english

File:

PDF, 11.20 MB

english, 2003

11

Isodicentric Yp: prenatal diagnosis and outcome in 12 cases

H. Bruyère, M. D. Speevak, E. J. T. Winsor, B. de Fréminville, S. A. Farrell, J. McGowan-Jordan, B. McGillivray, D. Chitayat, D. McFadden, V. Adouard, D. Terespolsky, F. Prieur, T. Pantzar, M. Hryncha

Journal:

Prenatal Diagnosis

Year:

2006

Language:

english

File:

PDF, 79 KB

english, 2006

12

An algorithm for the prenatal detection of chromosome anomalies by QF-PCR and G-banded analysis

M. D. Speevak, J. Dolling, D. Terespolsky, A. Blumenthal, S. A. Farrell

Journal:

Prenatal Diagnosis

Year:

2008

Language:

english

File:

PDF, 82 KB

english, 2008

13

The detection of chromosome anomalies by QF-PCR and residual risks as compared to G-banded analysis

Marsha D. Speevak, Jean McGowan-Jordan, Kathy Chun

Journal:

Prenatal Diagnosis

Year:

2011

Language:

english

File:

PDF, 98 KB

english, 2011

14

Identification of the origin of double minutes in normal human cells by laser-based chromosome microdissection approach

Evica Rajcan-Separovic, Hung-Shu Wang, Marsha D. Speevak, Lynn Janes, Robert G. Korneluk, Kyo Wakasa, Joh-E. Ikeda

Journal:

Year:

1995

Language:

english

File:

PDF, 1.98 MB

english, 1995

15

Alternatively spliced, truncated human BRCA2 isoforms contain a novel coding exon

Speevak, Marsha D, Young, Sean S, Feilotter, Harriet, Ainsworth, Peter

Journal:

European Journal of Human Genetics

Year:

2003

Language:

english

File:

PDF, 126 KB

english, 2003

16

Detection at amniocentesis of a maternally inherited X; Y translocation

M. Speevak, B. Clifford, D. M. Cox, A. G. W. Hunter

Journal:

Clinical Genetics

Year:

1985

Language:

english

File:

PDF, 338 KB

english, 1985

17

Stable Transfer of Zebrafish Chromosome Segments into Mouse Cells

Marc Ekker, Marsha D. Speevak, C.Cristofre Martin, Lucille Joly, Genny Giroux, Mario Chevrette

Journal:

Year:

1996

Language:

english

File:

PDF, 257 KB

english, 1996

18

Mosaic tetrasomy 21 in a liveborn male infant

Alasdair G. W. Hunter, Brian Clifford, Marsha Speevak, S. Brock MacMurray

Journal:

Clinical Genetics

Year:

1982

Language:

english

File:

PDF, 569 KB

english, 1982

19

The BRCA1S1715N mutation segregates with breast and ovarian cancer in an extended family pedigree

J Campbell, MD Speevak

Journal:

Clinical Genetics

Year:

2012

Language:

english

File:

PDF, 503 KB

english, 2012

20

Detection of submicroscopic aberrations in patients with unexplained mental retardation by fluorescence in situ hybridization using multiple subtelomeric probes

Fan, Yao-Shan, Zhang, Yang, Speevak, Marsha, Farrell, Sandra, Jung, Jack H, Siu, Victoria M

Journal:

Genetics in Medicine

Year:

2001

Language:

english

File:

PDF, 785 KB

english, 2001

21

Charcot–Marie–Tooth 1B caused by expansion of a familial myelin protein zero (MPZ) gene duplication

Speevak, Marsha D., Farrell, Sandra A.

Journal:

European Journal of Medical Genetics

Year:

2013

Language:

english

File:

PDF, 506 KB

english, 2013

22

Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays

Costain, G., Lionel, A. C., Merico, D., Forsythe, P., Russell, K., Lowther, C., Yuen, T., Husted, J., Stavropoulos, D. J., Speevak, M., Chow, E. W. C., Marshall, C. R., Scherer, S. W., Bassett, A. S.

Journal:

Human Molecular Genetics

Year:

2013

Language:

english

File:

PDF, 668 KB

english, 2013

23

Rank correlation inequalities with missing data

Papaioannou, Takis, Speevak, Ted

Journal:

Communication in Statistics- Theory and Methods

Year:

1977

Language:

english

File:

PDF, 137 KB

english, 1977

24

Book reviews

Eterno, John A., Peake, Gordon, Speevak, Allan R.

Journal:

Police Practice and Research

Year:

2008

Language:

english

File:

PDF, 72 KB

english, 2008

25

Identification of chromosomes implicated in suppression of apoptosis in somatic cell hybrids

Speevak, Marsha D., Chevrette, Mario

Journal:

Biochemistry and Cell Biology

Year:

1994

Language:

english

File:

PDF, 1.17 MB

english, 1994

26

A Note on Rank Correlation Inequalities with Missing Data

Speevak, Ted, Papaioannou, Takis

Journal:

Communication in Statistics- Theory and Methods

Year:

2015

Language:

english

File:

PDF, 75 KB

english, 2015

27

Midtrimester genetic amniocentesis in eastern Ontario: a review from 1970 to 1985.

Hunter, A G, Thompson, D, Speevak, M

Journal:

Journal of Medical Genetics

Year:

1987

Language:

english

File:

PDF, 1.11 MB

english, 1987

28

An Efficient Algorithm for Obtaining the Volume of a Special Kind of Pyramid and Application to Convex Polyhedra

Journal:

Mathematics of Computation

Year:

1986

Language:

english

File:

PDF, 201 KB

english, 1986

29

Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression

Lowther, Chelsea, Speevak, Marsha, Armour, Christine M., Goh, Elaine S., Graham, Gail E., Li, Chumei, Zeesman, Susan, Nowaczyk, Malgorzata J.M., Schultz, Lee-Anne, Morra, Antonella, Nicolson, Rob, Bik

Journal:

Genetics in Medicine

Year:

2016

Language:

english

File:

PDF, 738 KB

english, 2016

30

Human chromosome 3 mediates growth arrest and suppression of apoptosis in microcell hybrids.

Speevak, M D, Chevrette, M

Journal:

Molecular and Cellular Biology

Year:

1996

Language:

english

File:

PDF, 696 KB

english, 1996

31

Further evidence that a 100 Kb critical region is responsible for developmental delay, seizures, and dysmorphic features in 1q43q44 deletion patients

Speevak, M.D., Zeesman, S., Leonard, N., Nowaczyk, M.J.

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 165 KB

english, 2013

32

Construction and analysis of microcell hybrids containing dual selectable tagged human chromosomes

Speevak, M.D., B&eacute, rub&eacute, , N.G., McGowan-Jordan, I.J., Bisson, C., Lupton, S.D., Chevrette, M.

Journal:

Cytogenetic and Genome Research

Year:

1995

File:

PDF, 507 KB

1995

33

Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR)

Lebo, Matthew S, Zakoor, Kathleen-Rose, Chun, Kathy, Speevak, Marsha D, Waye, John S, McCready, Elizabeth, Parboosingh, Jillian S, Lamont, Ryan E, Feilotter, Harriet, Bosdet, Ian, Tucker, Tracy, Young

Journal:

Genetics in Medicine

Year:

2017

Language:

english

File:

PDF, 845 KB

english, 2017

34

Inequalities for sums of squares of reranked differences involving ties and missing data

Journal:

Communication in Statistics- Theory and Methods

Year:

2017

Language:

english

File:

PDF, 632 KB

english, 2017

35

Prenatal genomic microarray and sequencing in Canadian medical practice: towards consensus

Buchanan, Janet A, Chitayat, David, Kolomietz, Elena, Lee, Hin C, Scherer, Stephen W, Speevak, Marsha D, Sroka, Hana, Stavropoulos, Dimitri J

Journal:

Journal of Medical Genetics

Year:

2015

Language:

english

File:

PDF, 325 KB

english, 2015

36

MG-123 Exonic and intronic NRXN1 deletions: Novel genotype-phenotype correlations

Lowther, Chelsea, Speevak, Marsha, Armour, Christine, Goh, Elaine, Graham, Gail, Li, Chumei, Zeesman, Susan, Nowaczyk, Malgorzata JM, Schultz, Lee-Anne, Morra, Antonella, Nicolson, Robert, Rajguru, Ma

Journal:

Journal of Medical Genetics

Year:

2015

Language:

english

File:

PDF, 59 KB

english, 2015

37

Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia

Lowther, Chelsea, Merico, Daniele, Costain, Gregory, Waserman, Jack, Boyd, Kerry, Noor, Abdul, Speevak, Marsha, Stavropoulos, Dimitri J., Wei, John, Lionel, Anath C., Marshall, Christian R., Scherer,

Journal:

Genome Medicine

Year:

2017

Language:

english

File:

PDF, 598 KB

english, 2017

38

A new combinatorial identity

Sinyor, Joseph, Speevak, Ted, Tefera, Akalu

Journal:

International Journal of Mathematics and Mathematical Sciences

Year:

2001

Language:

english

File:

PDF, 1.79 MB

english, 2001

39

An unusual case of alpha-1-antitrypsin deficiency: SZ/Z

Speevak, M.D., DeMarco, M.L., Wiebe, N.S., Chapman, K.R.

Journal:

Clinical Biochemistry

Year:

2018

Language:

english

File:

PDF, 4.66 MB

english, 2018

40

NullCanada: A novel Î±1-antitrypsin allele with in cis variants Glu366Lys and Ile100Asn

Chen, Sharon, DeMarco, Mari L., Estey, Mathew P., Kyle, Barry, Parker, Michelle L., Agbor, Terence A., Kawada, Patricia, Speevak, Marsha, Nelson, Tanya N., Mattman, Andre

Journal:

Clinical Biochemistry

Year:

2020

Language:

english

File:

PDF, 2.96 MB

english, 2020

41

A fourth case of Feingold syndrome type 2: psychiatric presentation and management

Ganjavi, H., Siu, V. M., Speevak, M., MacDonald, P. A.

Journal:

Year:

2014

File:

PDF, 479 KB

2014

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