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51

TMEM237 Is Mutated in Individuals with a Joubert Syndrome Related Disorder and Expands the Role of the TMEM Family at the Ciliary Transition Zone

Lijia Huang, Katarzyna Szymanska, Victor L. Jensen, Andreas R. Janecke, A. Micheil Innes, Erica E. Davis, Patrick Frosk, Chunmei Li, Jason R. Willer, Bernard N. Chodirker, Cheryl R. Greenberg, D. Ross

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 2.05 MB

english, 2011

52

Life without amniocentesis: elevated maternal serum α-fetoprotein in the Manitoba program 1986–91

P. M. Kyle, Dr C. R. Harman, J. A. Evans, K. MacDonald, S. M. Menticoglou, F. A. Manning, B. N. Chodirker

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

1994

File:

PDF, 658 KB

1994

53

Antigenic differences between normal human albumin and a genetic variant

D. H. Naylor, C. A. Anhorn, C. Laschinger, F. Males, W. B. Chodirker

Journal:

Transfusion (Wiley)

Year:

1982

Language:

english

File:

PDF, 1.03 MB

english, 1982

54

Maternal serum alpha-fetoprotein levels in fetal hydrocephalus: a retrospective population based study

Terrence P Szajkowski, Bernard N Chodirker, Karen M MacDonald, Jane A Evans

Journal:

BMC Pregnancy and Childbirth

Year:

2006

Language:

english

File:

PDF, 222 KB

english, 2006

55

Fragile 19p13 in a family with mental illness

B. N. Chodirker, A. E. Chudley, M. Ray, D. E. Wickstrom, D. L. Riordan

Journal:

Clinical Genetics

Year:

1987

Language:

english

File:

PDF, 1.08 MB

english, 1987

56

A Homoallelic Gly317 → Asp Mutation in ALPL Causes the Perinatal (Lethal) Form of Hypophosphatasia in Canadian Mennonites

Cheryl R. Greenberg, Cheryl L.D. Taylor, James C. Haworth, Lorne E. Seargeant, Sylvia Philipps, Barbara Triggs-Raine, Bernard N. Chodirker

Journal:

Year:

1993

File:

PDF, 253 KB

1993

57

Refinement of the hereditary xerocytosis locus on chromosome 16q in a large Canadian kindred

B.L. Houston, T. Zelinski, S.J. Israels, G. Coghlan, B.N. Chodirker, P.G. Gallagher, D.S. Houston, R. Zarychanski

Journal:

Blood Cells, Molecules, and Diseases

Year:

2011

Language:

english

File:

PDF, 579 KB

english, 2011

58

An unadjusted NNT was a moderately good predictor of health benefit

Christopher A.K.Y. Chong, George Tomlinson, Lisa Chodirker, Nassi Figdor, Mark Uster, Gary Naglie, Murray D. Krahn

Journal:

Journal of Clinical Epidemiology

Year:

2006

Language:

english

File:

PDF, 221 KB

english, 2006

59

Angioimmunoblastic lymphadenopathy in a child with unusual clinical and immunologic features

CHODIRKER, W, KOMAR, R

Journal:

Journal of Allergy and Clinical Immunology

Year:

1985

Language:

english

File:

PDF, 926 KB

english, 1985

60

Reply

Journal:

Journal of Allergy and Clinical Immunology

Year:

1988

Language:

english

File:

PDF, 76 KB

english, 1988

61

The C677T methylenetetrahydrofolate reductase variant and third trimester obstetrical complications in women with unexplained elevations of maternal serum alpha-fetoprotein

Natalie K Björklund, Jane A Evans, Cheryl R Greenberg, Lorne E Seargeant, Carol E Schneider, Bernard N Chodirker

Journal:

Reproductive Biology and Endocrinology

Year:

2004

Language:

english

File:

PDF, 227 KB

english, 2004

62

Gamma-Globulins: Quantitative Relationships in Human Serum and Nonvascular Fluids

Chodirker, W. B., Tomasi, T. B.

Journal:

Year:

1963

Language:

english

File:

PDF, 745 KB

english, 1963

63

Origin of a Prenatal Mosaic Supernumerary Neocentromeric Derivative Chromosome 13 Determined by QF-PCR

Dawson, A.J., Hryshko, M., Konkin, D., Bal, S., Bernier, D., Tomiuk, M., Burnett, S., Frosk, P., Chodirker, B.N., Chun, K.

Journal:

Fetal Diagnosis and Therapy

Year:

2013

Language:

english

File:

PDF, 272 KB

english, 2013

64

P-265 A Canadian survey of primary care physicians knowledge, workup and referral patterns in elderly patients with MDS and unexplained cytopenias

Chodirker, L., Wells, R., Buckstein, R.

Journal:

Leukemia Research

Year:

2013

Language:

english

File:

PDF, 64 KB

english, 2013

65

Fluticasone propionate: a large multicentre trial

Dolovich, J., Anderson, M., Chodirker, W., Drouin, M., Hargreave, F.E., Hebert, J., Knight, A., O'Conner, M., Small, P., Yang, W.

Journal:

Respiratory Medicine

Year:

1990

Language:

english

File:

PDF, 106 KB

english, 1990

66

Lenalidomide and metronomic melphalan for CMML and higher risk MDS: A phase 2 clinical study with biomarkers of angiogenesis

Buckstein, Rena, Kerbel, Robert, Cheung, Matthew, Shaked, Yuval, Chodirker, Lisa, Lee, Christina R., Lenis, Martha, Davidson, Cindy, Cussen, Mary-Anne, Reis, Marciano, Chesney, Alden, Zhang, Liying, M

Journal:

Leukemia Research

Year:

2014

Language:

english

File:

PDF, 1.35 MB

english, 2014

67

P-116 Frailty is an independent prognostic marker for overall survival in MDS: Results of a Canadian MDS registry

Buckstein, R., Prica, A., Chodirker, L., Zhu, N., Nevill, T., Leitch, H., Yee, K., Leber, B.F., Sabloff, M., Kumar, R., Geddes, M., Lenis, M., Li, C., Mamedov, A., Khalaf, D., Zhang, L., Rockwood, K.,

Journal:

Leukemia Research

Year:

2013

Language:

english

File:

PDF, 136 KB

english, 2013

68

P-257 The effects of azacitidine on quality of life: A prospective longitudinal assessment

Prica, A., Tseng, E., Wells, R., Alibhai, S., Lam, A., Mamedov, A., Chodirker, L., Zhang, L., Khalaf, D., Lenis, M., Buckstein, R.

Journal:

Leukemia Research

Year:

2013

Language:

english

File:

PDF, 138 KB

english, 2013

69

P-317 Immunosuppressive therapy for patients with myelodysplastic syndrome: A single centre experience

Prica, A., Wells, R., Buckstein, R., Chodirker, L.

Journal:

Leukemia Research

Year:

2013

Language:

english

File:

PDF, 68 KB

english, 2013

70

Infantile hypophosphatasia—Linkage with the RH locus

Chodirker, B.N., Evans, J.A., Lewis, M., Coghlan, G., Belcher, E., Philipps, S., Seargeant, L.E., Sus, C., Greenberg, C.R.

Journal:

Year:

1987

Language:

english

File:

PDF, 263 KB

english, 1987

71

MSAFP Levels in Aboriginal Canadian Women

B.N. Chodirker, L.B. Erdile, K.M. MacDonald, C.R. Harman, M.S. Cheang and J.A. Evans

Journal:

Canadian Journal of Public Health / Revue Canadienne de Sante'e Publique

Year:

1994

Language:

english

File:

PDF, 869 KB

english, 1994

72

Evaluation of a Clinical Genetics Service – A Quality Initiative

Elliott, Alison M., Chodirker, Bernard N., Bocangel, Patricia, Mhanni, Aizeddin A.

Journal:

Journal of Genetic Counseling

Year:

2014

Language:

english

File:

PDF, 197 KB

english, 2014

73

The Floppy Infant: Retrospective Analysis of Clinical Experience (1990--2000) in a Tertiary Care Facility

Birdi, K., Prasad, A. N., Prasad, C., Chodirker, B., Chudley, A. E.

Journal:

Journal of Child Neurology

Year:

2005

Language:

english

File:

PDF, 453 KB

english, 2005

74

Radiographic characterization of the hands in Ritscher-Schinzel/3-C syndrome

Kaitlyn J Friesen,Bernard N Chodirker,Albert E Chudley,Martin H Reed…

Journal:

Year:

2013

Language:

english

File:

PDF, 246 KB

english, 2013

75

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

Elliott, A. M., Simard, L. R., Coghlan, G., Chudley, A. E., Chodirker, B. N., Greenberg, C. R., Burch, T., Ly, V., Hatch, G. M., Zelinski, T.

Journal:

Journal of Medical Genetics

Year:

2013

Language:

english

File:

PDF, 1.01 MB

english, 2013

76

Efficacy, toxicity and mortality of autologous SCT in multiple myeloma patients with dialysis-dependent renal failure

St Bernard, R, Chodirker, L, Masih-Khan, E, Jiang, H, Franke, N, Kukreti, V, Tiedemann, R, Trudel, S, Reece, D, Chen, C I

Journal:

Bone Marrow Transplantation

Year:

2015

Language:

english

File:

PDF, 360 KB

english, 2015

77

Iron overload in myelodysplastic syndromes

Chodirker, Lisa, Wells, Richard A

Journal:

Expert Review of Hematology

Year:

2009

Language:

english

File:

PDF, 342 KB

english, 2009

78

The epidemiology of intermittent and chronic ataxia in children in Manitoba, Canada

Salman, Michael S, Lee, Esther J, Tjahjadi, Anindita, Chodirker, Bernard N

Journal:

Developmental Medicine & Child Neurology

Year:

2013

Language:

english

File:

PDF, 282 KB

english, 2013

79

Scientific correspondence

Frosk, Patrick, Phillips, Susan M., Del Bigio, Marc R., Chodirker, Bernard N.

Journal:

Neuropathology and Applied Neurobiology

Year:

2014

Language:

english

File:

PDF, 430 KB

english, 2014

80

Initial transfusion intensity predicts survival in myelodysplastic syndrome

Chan, Lap Shu Alan, Shapiro, Roman, Buckstein, Rena, Lin, Yulia, Callum, Jeannie, Chodirker, Lisa, Lee, Christina D., Prica, Anca, Lam, Adam, Mamedov, Alexandre, Wells, Richard A.

Journal:

Leukemia and Lymphoma

Year:

2014

Language:

english

File:

PDF, 1.03 MB

english, 2014

81

A homozygous PMS2 founder mutation with an attenuated constitutional mismatch repair deficiency phenotype

Li, L., Hamel, N., Baker, K., McGuffin, M. J., Couillard, M., Gologan, A., Marcus, V. A., Chodirker, B., Chudley, A., Stefanovici, C., Durandy, A., Hegele, R. A., Feng, B.-J., Goldgar, D. E., Zhu, J.,

Journal:

Journal of Medical Genetics

Year:

2015

Language:

english

File:

PDF, 1.19 MB

english, 2015

82

Congenital hydrocephalus secondary to Walker-Warburg syndrome identified on the Manitoba Neonatal Screening Programme for Duchenne muscular dystrophy.

Greenberg, C R, Jacobs, H K, Nylen, T E, Gibb, M, Chodirker, B N, Moffatt, M, Lacson, A, Halliday, W, Bernier, F, el-Husseini, A

Journal:

Journal of Medical Genetics

Year:

1992

Language:

english

File:

PDF, 963 KB

english, 1992

83

Increased Nuchal Translucency Thickness: A Potential Indicator for Ritscher-Schinzel Syndrome

Rusnak, Alison J., Hadfield, Marie I., Chudley, Albert E., Marles, Sandra L., Reid, Gregory J., Chodirker, Bernard N.

Journal:

Fetal Diagnosis and Therapy

Year:

2008

Language:

english

File:

PDF, 138 KB

english, 2008

84

Response to Correspondence on "Lissencephaly With Brainstem and Cerebellar Hypoplasia and Congenital Cataracts"

Salman, M. S., Abumansour, I. S., Chudley, A. E., Chodirker, B. N., Wrogemann, J.

Journal:

Journal of Child Neurology

Year:

2015

Language:

english

File:

PDF, 50 KB

english, 2015

85

Lissencephaly With Brainstem and Cerebellar Hypoplasia and Congenital Cataracts

Abumansour, I. S., Wrogemann, J., Chudley, A. E., Chodirker, B. N., Salman, M. S.

Journal:

Journal of Child Neurology

Year:

2014

Language:

english

File:

PDF, 192 KB

english, 2014

86

Hereditary colorectal cancer registries in Canada: report from the Colorectal Cancer Association of Canada consensus meeting; Montreal, Quebec; October 28, 2011

Rothenmund, H., Singh, H., Candas, B., Chodirker, B., Serfas, K., Aronson, M., Holter, S., Volenik, A., Green, J., Dicks, E., Woods, M.O., Gilchrist, D., Gryfe, R., Cohen, Z., Foulkes, W.D.

Journal:

Current Oncology

Year:

2013

Language:

english

File:

PDF, 6.17 MB

english, 2013

87

Disrupted auto-regulation of the spliceosomal gene SNRPB causes cerebro–costo–mandibular syndrome

Lynch, Danielle C., Revil, Timothée, Schwartzentruber, Jeremy, Bhoj, Elizabeth J., Innes, A. Micheil, Lamont, Ryan E., Lemire, Edmond G., Chodirker, Bernard N., Taylor, Juliet P., Zackai, Elaine H., M

Journal:

Nature Communications

Year:

2014

Language:

english

File:

PDF, 776 KB

english, 2014

88

Neuro-Ophthalmological Findings in Children and Adolescents with Chronic Ataxia

Salman, Michael S., Chodirker, Bernard N.

Journal:

Neuro-Ophthalmology

Year:

2015

Language:

english

File:

PDF, 408 KB

english, 2015

89

Very Low Second-Trimester Maternal Serum Alpha-fetoprotein

Baschat, Ahmet A., Harman, Chris R., Farid, Gehan, Chodirker, Bernard N., Evans, Jane A.

Journal:

Obstetrics & Gynecology

Year:

2002

Language:

english

File:

PDF, 167 KB

english, 2002

90

Prenatal Diagnosis of Walker–Warburg Syndrome Using Single Nucleotide Polymorphism Array: A Clinical Experience from Three Related Palestinian Families with Congenital Hydrocephalus

Abumansour, Iman, Al Sulmi, Eman, Chodirker, Bernard, Hunt, Jennifer

Journal:

American Journal of Perinatology Reports

Year:

2015

Language:

english

File:

PDF, 239 KB

english, 2015

91

Ethnicity and Geographic Distribution of Pediatric Chronic Ataxia in Manitoba

Salman, Michael S., Masood, Shaheen, Azad, Meghan, Chodirker, Bernard N.

Journal:

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques

Year:

2014

File:

PDF, 3.91 MB

2014

92

Neuroimaging Findings and Repeat Neuroimaging Value in Pediatric Chronic Ataxia

Salman, Michael S, Chodirker, Bernard N, Bunge, Martin

Journal:

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques

Year:

2016

File:

PDF, 244 KB

2016

93

Severe hemihypotrophy in a female infant with mosaic Turner syndrome: a variant of Russell???Silver syndrome?

Li, Chumei C., Chodirker, Bernard N., Dawson, Angelika J., Chudley, Albert E.

Journal:

Clinical Dysmorphology

Year:

2004

Language:

english

File:

PDF, 143 KB

english, 2004

94

Proposed Guideline for Fetal Choroid Plexus Cysts

Chodirker, B.N., Evans, J.A., McRae, A.R.

Journal:

Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstétrique et gynécologie du Canada : JOGC

Year:

2006

Language:

english

File:

PDF, 56 KB

english, 2006

95

Letters to the Editor

Chudley, Albert E., Dawson, Angelika J., Chodirker, Bernard N., Jocelyn, Leslie J.

Journal:

Journal of Developmental & Behavioral Pediatrics

Year:

1999

File:

PDF, 476 KB

1999

96

Familial Neuroblastoma

Lemire, Edrnond G., Chodirker, Bernard N., Williams, Gaynor J., Seargeant, Lome E., Israels, Sara J., Phillips, Susan M., de Nanassy, Joseph A., Maris, John M., Yanofsky, Rochelle A.

Journal:

Journal of Pediatric Hematology/Oncology

Year:

1998

File:

PDF, 409 KB

1998

97

Outcomes of Genetic Evaluation in Children with Pervasive Developmental Disorder

CHUDLEY, ALBERT E., GUTIERREZ, ERNESTO, JOCELYN, LESLIE J., CHODIRKER, BERNARD N.

Journal:

Journal of Developmental & Behavioral Pediatrics

Year:

1998

File:

PDF, 1.12 MB

1998

98

Le diagnostic prénatal 2001: l’Odyssée continue

Journal:

Year:

2001

File:

PDF, 179 KB

2001

99

Prenatal Diagnosis 2001: The Odyssey Continues

Journal:

Year:

2001

Language:

english

File:

PDF, 160 KB

english, 2001

100

A truncating mutation in CEP55 is the likely cause of MARCH, a novel syndrome affecting neuronal mitosis

Frosk, Patrick, Arts, Heleen H, Philippe, Julien, Gunn, Carter S, Brown, Emma L, Chodirker, Bernard, Simard, Louise, Majewski, Jacek, Fahiminiya, Somayyeh, Russell, Chad, Liu, Yangfan P, Hegele, Rober

Journal:

Journal of Medical Genetics

Year:

2017

Language:

english

File:

PDF, 2.67 MB

english, 2017