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1

Meckel syndrome in the Hutterite population is actually a Joubert-related cerebello-oculo-renal syndrome

Kym M. Boycott, Jillian S. Parboosingh, James N. Scott, D. Ross McLeod, Cheryl R. Greenberg, T. Mary Fujiwara, Jean K. Mah, Julian Midgley, Andrew Wade, Francois P. Bernier, Bernard N. Chodirker, Mart

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 227 KB

english, 2007

2

Very low second-trimester maternal serum alpha-fetoprotein: Association with high birth weight

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

Journal:

Obstetrics & Gynecology

Year:

2002

Language:

english

File:

PDF, 167 KB

english, 2002

3

Routine genetic testing for Asperger syndrome

Chodirker, Bernard N, Chudley, Albert E

Journal:

Genetics in Medicine

Year:

2008

Language:

english

File:

PDF, 180 KB

english, 2008

4

Low MSAFP levels and Williams syndrome

Chodirker, Bernard N., Greenberg, Cheryl R., Giddins, Niels G., Dawson, Angelika J., Evans, Jane A., Chudley, Albert E.

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 22 KB

english, 1997

5

Fetal hepatic haemangioendothelioma: a new association with elevated maternal serum alpha-fetoprotein

Aizeddin A. Mhanni, Bernard N. Chodirker, Jane A. Evans, Savas Menticouglou, Nathan Wiseman, Nigel MacDonald, Albert E. Chudley

Journal:

Prenatal Diagnosis

Year:

2000

Language:

english

File:

PDF, 55 KB

english, 2000

6

Severe acro-renal-uterine-mandibular syndrome

Jane A. Evans, Susan Phillips, Martin Reed, Bernard N. Chodirker

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 459 KB

english, 2000

7

A not-so-“new” mental retardation syndrome

Bernard N. Chodirker, Sandra L. Marles, Albert E. Chudley

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 31 KB

english, 2002

8

Zimmerman-Laband syndrome and profound mental retardation

Bernard N. Chodirker, Dr. Albert E. Chudley, Milada A. Toffler, Martin H. Reed, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1986

Language:

english

File:

PDF, 373 KB

english, 1986

9

Possible prenatal hydantoin effect in a child born to a nonepileptic mother

Bernard N. Chodirker, Dr. Albert E. Chudley, Martin H. Reed, T. V. N. Persaud, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1987

Language:

english

File:

PDF, 809 KB

english, 1987

10

Developmental delay, short stature, and minor facial anomalies in a child with ring chromosome 16

Bernard N. Chodirker, Manoranjan Ray, Phyllis J. McAlpine, Diane Riordan, Alice Vust, Dora Pugh, Dr. Albert E. Chudley, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1988

Language:

english

File:

PDF, 419 KB

english, 1988

11

Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome

J. Stephen Bamforth, Claire O. Leonard, Bernard N. Chodirker, David Chitayat, Hilda L. Gritter, Jane A. Evans, Beth Keena, Tapio Pantzar, Jan M. Friedman, Judith G. Hall, John M. Opitz, James F. Reyno

Journal:

American Journal of Medical Genetics Part A

Year:

1989

Language:

english

File:

PDF, 774 KB

english, 1989

12

Absence of excess chromosome breakage in a patient with VACTERL-hydrocephalus

Dr. Jane A. Evans, Bernard N. Chodirker

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 159 KB

english, 1993

13

Male-to-male transmission of mild Bachmann-de Lange syndrome

Bernard N. Chodirker, Albert E. Chudley

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 502 KB

english, 1994

14

Evidence for Ritscher-Schinzel syndrome in Canadian native Indians

Dr. Sandra L. Marles, Bernard N. Chodirker, Cheryl R. Greenberg, Albert E. Chudley

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 757 KB

english, 1995

15

Another case of Varadi–Papp Syndrome with a molar tooth sign

Bernard N. Chodirker, Namrata S. Shah, Martin K. Bunge, Martin H. Reed

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 54 KB

english, 2005

16

Clinical and epidemiological findings in patients with central ray deficiency: Split hand foot malformation (SHFM) in Manitoba, Canada

Alison M. Elliott, Martin H. Reed, Albert E. Chudley, Bernard N. Chodirker, Jane A. Evans

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 161 KB

english, 2006

17

Manitoba oculotrichoanal (MOTA) syndrome: Report of eight new cases

Chumei Li, Sandra L Marles, Cheryl R. Greenberg, Bernard N. Chodirker, Jiddeke van de Kamp, Anne Slavotinek, Albert E. Chudley

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 199 KB

english, 2007

18

Unusual dicentric chromosome 22 associated with a 22q13 deletion

Tina Babineau, Heather L. Wilson, Angelika J. Dawson, Bernard N. Chodirker, Vazken M. Der Kaloustian, Suzanne Demczuk, Heather E. McDermid

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 164 KB

english, 2006

19

Potential teratogenic effects of allopurinol: A case report

Mariya Kozenko, David Grynspan, Titi Oluyomi-Obi, Daniel Sitar, Alison M. Elliott, Bernard N. Chodirker

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 425 KB

english, 2011

20

Infantile muscular dystrophy in Canadian aboriginals is an αB-crystallinopathy

Marc R. Del Bigio, Albert E. Chudley, Harvey B. Sarnat, Craig Campbell, Sharan Goobie, Bernard N. Chodirker, Duygu Selcen

Journal:

Annals of Neurology

Year:

2011

Language:

english

File:

PDF, 313 KB

english, 2011

21

Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype

Chitra Prasad, Asuri N Prasad, Bernard N Chodirker, Christine Lee, Angelika K Dawson, Leslie J Jocelyn, Albert E Chudley

Journal:

Clinical Genetics

Year:

2000

Language:

english

File:

PDF, 204 KB

english, 2000

22

Screening for open neural tube defects from 21 to 25 weeks' gestation: the Manitoba experience

Natalie K. Björklund, Karen M. MacDonald, Jane A. Evans, Carol E. Schneider, Bernard N. Chodirker

Journal:

Prenatal Diagnosis

Year:

2005

Language:

english

File:

PDF, 77 KB

english, 2005

23

Survival of fetuses with abnormal karyotypes and cystic hygromas detected prenatally

Bernard N. Chodirker, Christopher R. Harman, Cheryl R. Greenberg

Journal:

Prenatal Diagnosis

Year:

1990

Language:

english

File:

PDF, 90 KB

english, 1990

24

Linkage analysis of X-linked cleft palate and ankyloglossia in Manitoba Mennonite and British Columbia Native kindreds

Sharon M. Gorski, Karen J. Adams, Patricia H. Birch, Bernard N. Chodirker, Cheryl R. Greenberg, Paul J. Goodfellow

Journal:

Year:

1994

Language:

english

File:

PDF, 1.09 MB

english, 1994

25

Agenesis of the corpus callosum and cerebral anomalies in inborn errors of metabolism

Asuri N. Prasad, Kelly Bunzeluk, Chitra Prasad, Bernard N. Chodirker, Kenneth G. Magnus, Cheryl R. Greenberg

Journal:

Congenital Anomalies

Year:

2007

Language:

english

File:

PDF, 272 KB

english, 2007

26

Fetal Hydrocephalus Caused by Cryptic Intraventricular Hemorrhage

Belinda Lategan, Bernard N. Chodirker, Marc R. Del Bigio

Journal:

Brain Pathology

Year:

2010

Language:

english

File:

PDF, 1.08 MB

english, 2010

27

Risk factors for nonsyndromic holoprosencephaly: A Manitoba case–control study

Simone S. Vaz, Bernard Chodirker, Chitra Prasad, Jamie A. Seabrook, Albert E. Chudley, Asuri N. Prasad

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 117 KB

english, 2012

28

Prenatal screening characteristics in Emanuel syndrome: a case series and review of the literature

Walfisch, Asnat, Mills, Kelsey E., Chodirker, Bernard N., Berger, Howard

Journal:

Archives of Gynecology and Obstetrics

Year:

2012

Language:

english

File:

PDF, 150 KB

english, 2012

29

Trends in Telehealth versus On-site Clinical Genetics Appointments in Manitoba: A Comparative Study

Alison M. Elliott, Aizeddin A. Mhanni, Sandra L. Marles, Cheryl R. Greenberg, Albert E. Chudley, Gwendolyne C. Nyhof, Bernard N. Chodirker

Journal:

Journal of Genetic Counseling

Year:

2012

Language:

english

File:

PDF, 402 KB

english, 2012

30

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

31

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

32

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

33

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

34

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

35

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

36

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

37

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

38

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

39

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

40

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

41

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

42

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

43

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

44

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

45

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

46

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

47

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

48

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

49

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

50

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

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