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Deficiency of Innate and Acquired Immunity Caused by an IKBKB Mutation

The New England journal of medicine, 2013-12, Vol.369 (26), p.2504-2514

2013

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Identification of Claudin 1 Transcript Variants in Human Invasive Breast Cancer

PloS one, 2016-09, Vol.11 (9), p.e0163387-e0163387

2016

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GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome

American journal of human genetics, 2012-06, Vol.90 (6), p.1088-1093

2012

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Delineating the role of alterations in lipid metabolism to the pathogenesis of inherited skeletal and cardiac muscle disorders

Journal of lipid research, 2012-01, Vol.53 (1), p.4-27

2012

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Mutation of a Gene Essential for Ribosome Biogenesis, EMG1, Causes Bowen-Conradi Syndrome

American journal of human genetics, 2009-06, Vol.84 (6), p.728-739

2009

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The c.64_80del SMIM1 allele is segregating in the Hutterite population

Transfusion (Philadelphia, Pa.), 2016-04, Vol.56 (4), p.946-949

2016

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The c.64_80del SMIM1 allele is segregating in the H utterite population

Transfusion (Philadelphia, Pa.), 2016-04, Vol.56 (4), p.946-949

2016

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Development of a Population-Based Newborn Screening Method for Severe Combined Immunodeficiency in Manitoba, Canada

International journal of neonatal screening, 2018-06, Vol.4 (2), p.19-19

2018

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ABCG2 null alleles define the Jr(a―) blood group phenotype

Nature genetics, 2012-02, Vol.44 (2), p.131-132

2012

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A role for immunoglobulin G in donor-specific Streptococcus sanguis-induced platelet aggregation

Thrombosis and haemostasis, 2006-02, Vol.95 (2), p.288-293

2006

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A novel mutation in KIAA0196: identification of a gene involved in Ritscher–Schinzel/3C syndrome in a First Nations cohort

Journal of medical genetics, 2013-12, Vol.50 (12), p.819-822

2013

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Abstract 751: Identification of variant claudin 1 transcripts in human breast tumors

Cancer research (Chicago, Ill.), 2013-04, Vol.73 (8_Supplement), p.751-751

2013

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The JR blood group system (ISBT 032): molecular characterization of three new null alleles

Transfusion (Philadelphia, Pa.), 2013-07, Vol.53 (7), p.1575-1579

2013

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Alleles of the LAN blood group system: molecular and serologic investigations

Transfusion (Philadelphia, Pa.), 2014-02, Vol.54 (2), p.398-404

2014

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The JR blood group system: identification of alleles that alter expression

Transfusion (Philadelphia, Pa.), 2013-11, Vol.53 (11), p.2710-2714

2013

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Human Blood Group Genes 2010: Chromosomal Locations and Cloning Strategies Revisited

Transfusion medicine reviews, 2011, Vol.25 (1), p.36-46

2011

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Molecular Protocols in Transfusion Medicine

Transfusion (Philadelphia, Pa.), 2001-04, Vol.41 (4), p.573-573

Zelinski, Teresa

2001

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Molecular Protocols in Transfusion Medicine: Gregory A. Denomme, Maria Rios, and Marion E. Reid, editors. San Diego, CA: Academic Press, 2000. 186 pages. $69.95. Softcover

Transfusion (Philadelphia, Pa.), 2001-04, Vol.41 (4), p.573-573

Zelinski, Teresa

2001

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Genetic Linkage of the Dehydrated Hereditary Stomatocytosis Locus to Chromosome 16 in Two Kindreds and Refinement of the Candidate Gene Region to 16q24.2 - 16qter

Blood, 2011-11, Vol.118 (21), p.3170-3170

2011

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Phenotypic Evaluation of a Family Cohort with Hemolytic Anemia

Blood, 2010-11, Vol.116 (21), p.3214-3214

2010

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Molecular basis of the LOCR (Rh55) antigen

Transfusion (Philadelphia, Pa.), 2006-10, Vol.46 (10), p.1689-1692

2006

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The Association Between SHP-2 Mutations and Platelet Function in Noonan Syndrome

Blood, 2008-11, Vol.112 (11), p.1239-1239

2008

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Delineating the role of alterations in lipid metabolism to the pathogenesis of inherited skeletal and cardiac muscle disorders: Thematic Review Series: Genetics of Human Lipid Diseases

Journal of lipid research, 2012-01, Vol.53 (1), p.4-27

2012

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GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome

American journal of human genetics, 2012-07, Vol.91 (1), p.209-209

2012

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Human Blood Group Genes 2004: Chromosomal Locations and Cloning Strategies

Transfusion medicine reviews, 2005, Vol.19 (1), p.45-57

2005

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Deficiency of Innate and Acquired Immunity Caused by an IKBKB Mutation

Identification of Claudin 1 Transcript Variants in Human Invasive Breast Cancer

GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome

Delineating the role of alterations in lipid metabolism to the pathogenesis of inherited skeletal and cardiac muscle disorders

Mutation of a Gene Essential for Ribosome Biogenesis, EMG1, Causes Bowen-Conradi Syndrome

The c.64_80del SMIM1 allele is segregating in the Hutterite population

The c.64_80del SMIM1 allele is segregating in the H utterite population

Development of a Population-Based Newborn Screening Method for Severe Combined Immunodeficiency in Manitoba, Canada

ABCG2 null alleles define the Jr(a―) blood group phenotype

A role for immunoglobulin G in donor-specific Streptococcus sanguis-induced platelet aggregation

A novel mutation in KIAA0196: identification of a gene involved in Ritscher–Schinzel/3C syndrome in a First Nations cohort

Abstract 751: Identification of variant claudin 1 transcripts in human breast tumors

The JR blood group system (ISBT 032): molecular characterization of three new null alleles

Alleles of the LAN blood group system: molecular and serologic investigations

The JR blood group system: identification of alleles that alter expression

Human Blood Group Genes 2010: Chromosomal Locations and Cloning Strategies Revisited

Molecular Protocols in Transfusion Medicine

Molecular Protocols in Transfusion Medicine: Gregory A. Denomme, Maria Rios, and Marion E. Reid, editors. San Diego, CA: Academic Press, 2000. 186 pages. $69.95. Softcover

Genetic Linkage of the Dehydrated Hereditary Stomatocytosis Locus to Chromosome 16 in Two Kindreds and Refinement of the Candidate Gene Region to 16q24.2 - 16qter

Phenotypic Evaluation of a Family Cohort with Hemolytic Anemia

Molecular basis of the LOCR (Rh55) antigen

The Association Between SHP-2 Mutations and Platelet Function in Noonan Syndrome

Delineating the role of alterations in lipid metabolism to the pathogenesis of inherited skeletal and cardiac muscle disorders: Thematic Review Series: Genetics of Human Lipid Diseases

GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome

Human Blood Group Genes 2004: Chromosomal Locations and Cloning Strategies

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