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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

Second and first trimester estimation of risk for Down syndrome: implementation and performance in the SAFER study

Andrew R. MacRae, Bernie N. Chodirker, Gregory A. Davies, Glenn E. Palomaki, George J. Knight, Jane Minett, Peter A. Kavsak, Ants Toi, David Chitayat, Paul G. Van Caeseele

Journal:

Prenatal Diagnosis

Year:

2010

Language:

english

File:

PDF, 100 KB

english, 2010

3

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

4

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

5

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

6

Molecular and clinical correlation study of Williams-Beuren syndrome: No evidence of molecular factors in the deletion region or imprinting affecting clinical outcome

Wang, Michael S., Schinzel, Albert, Kotzot, Dieter, Balmer, Damina, Casey, Robin, Chodirker, Bernie N., Gyftodimou, Jolanda, Petersen, Michael B., Lopez-Rangel, Elana, Robinson, Wendy P.

Journal:

American Journal of Medical Genetics

Year:

1999

Language:

english

File:

PDF, 129 KB

english, 1999

7

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

8

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

9

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

10

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

11

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

12

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

13

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

14

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

15

Elevated MSAFP levels and congenital heart defects: Lack of an association

H. Albar, K. M. MacDonald, C. R. Harman, J. A. Evans, B. N. Chodirker

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 355 KB

english, 1994

16

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

17

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

18

Bowen–Conradi syndrome: A clinical and genetic study

R.B. Lowry, A.M. Innes, F.P. Bernier, D.R. McLeod, C.R. Greenberg, A.E. Chudley, B. Chodirker, S.L. Marles, M.J. Crumley, J.C. Loredo-Osti, K. Morgan, T.M. Fujiwara

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 348 KB

english, 2003

19

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

20

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

21

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

22

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

23

Clinical genetics and the Hutterite population: A review of Mendelian disorders

Kym M. Boycott, Jillian S. Parboosingh, Bernie N. Chodirker, R. Brian Lowry, D. Ross McLeod, Jackie Morris, Cheryl R. Greenberg, Albert E. Chudley, Francois P. Bernier, Julian Midgley, Lisbeth Birk Mø

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 193 KB

english, 2008

24

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

25

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

26

Factors affecting screen completion in two forms of integrated prenatal screening for Down syndrome in the safer study

P.A. Kavsak, A.R. MacRae, A. Toi, G.D. Davies, B.N. Chodirker, J. Minett, G.E. Palomaki, G.J. Knight, D. Chitayat, P.G. Van Caeseele

Journal:

Clinical Biochemistry

Year:

2010

Language:

english

File:

PDF, 61 KB

english, 2010

27

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

28

Monsters, myths and syndromes depicted on stamps

BN Chodirker, AE Chudley

Journal:

Clinical Genetics

Year:

2001

Language:

english

File:

PDF, 231 KB

english, 2001

29

Landmarks in genetics through philately: Down syndrome

AE Chudley, BN Chodirker

Journal:

Clinical Genetics

Year:

2003

Language:

english

File:

PDF, 9.52 MB

english, 2003

30

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

31

Spontaneous resolution of a cystic hygroma in a fetus with Turner syndrome

B. N. Chodirker, C. R. Harman, C. R. Greenberg

Journal:

Prenatal Diagnosis

Year:

1988

Language:

english

File:

PDF, 538 KB

english, 1988

32

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

33

Mosaic Isochromosome 20q found on amniocentesis with normal outcome

B. N. Chodirker, R. Jenkins

Journal:

Prenatal Diagnosis

Year:

1990

Language:

english

File:

PDF, 239 KB

english, 1990

34

MSAFP levels and oesophageal atresia

B. N. Chodirker, A. E. Chudley, K. M. Macdonald, C. R. Harman, J. A. Evans

Journal:

Prenatal Diagnosis

Year:

1994

Language:

english

File:

PDF, 300 KB

english, 1994

35

Paracentric inversion 11q in Canadian Hutterites

B. N. Chodirker, C. R. Greenberg, P. D. Pabello, A. E. Chudley

Journal:

Year:

1992

Language:

english

File:

PDF, 290 KB

english, 1992

36

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

37

Increased plasma pyridoxal-5′-phosphate levels before and after pyridoxine loading in carriers of perinatal/infantile hypophosphatasia

B. N. Chodirker, S. P. Coburn, L. E. Seargeant, M. P. Whyte, C. R. Greenberg

Journal:

Journal of Inherited Metabolic Disease

Year:

1990

Language:

english

File:

PDF, 463 KB

english, 1990

38

Computer assisted analysis of hand radiographs in infantile hypophosphatasia carriers

B. N. Chodirker, D. Roy, C. R. Greenberg, M. Cheang, J. A. Evans, M. H. Reed

Journal:

Pediatric Radiology

Year:

1991

Language:

english

File:

PDF, 448 KB

english, 1991

39

A large novel deletion in theAPCpromoter region causes gene silencing and leads to classical familial adenomatous polyposis in a Manitoba Mennonite kindred

George S. Charames, Lily Ramyar, Angela Mitri, Terri Berk, Hong Cheng, Jack Jung, Patricia Bocangel, Bernie Chodirker, Cheryl Greenberg, Elizabeth Spriggs, Bharati Bapat

Journal:

Year:

2008

Language:

english

File:

PDF, 399 KB

english, 2008

40

Immunological parameters and α1-antitrypsinin chronic urticaria

W. B. CHODIRKER, W. BAUMAN, R. R. KOMAR

Journal:

Clinical & Experimental Allergy

Year:

1979

Language:

english

File:

PDF, 523 KB

english, 1979

41

Cryptic chromosome rearrangements detected by subtelomere assay in patients with mental retardation and dysmorphic features

AJ Dawson, S. Putnam, J. Schultz, D. Riordan, C. Prasad, CR Greenberg, BN Chodirker, AA Mhanni, AE Chudley

Journal:

Clinical Genetics

Year:

2002

Language:

english

File:

PDF, 966 KB

english, 2002

42

Genetic landmarks through philately – epilepsy and clinical genetic issues

BN Chodirker, AE Chudley

Journal:

Clinical Genetics

Year:

2004

Language:

english

File:

PDF, 2.72 MB

english, 2004

43

Cytogenetic microarrays in Manitoba patients with developmental delay

AJ Dawson, D Riordan, M Tomiuk, D Konkin, T Anderson, P Bocangel, N Lwiwiski, J Saltel-Olson, S Marles, CR Greenberg, A Mhanni, BN Chodirker, AE Chudley

Journal:

Clinical Genetics

Year:

2009

Language:

english

File:

PDF, 71 KB

english, 2009

44

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

45

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

46

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

47

Frequency of FMR1 Premutations in a Consecutive Newborn Population by PCR Screening of Guthrie Blood Spots

A.J. Dawson, B.N. Chodirker, A.E. Chudley

Journal:

Biochemical and Molecular Medicine

Year:

1995

File:

PDF, 545 KB

1995

48

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

49

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

50

Gamma heavy chain disease and rheumatoid arthritis

John R. Dickson, Manfred Harth, David A. Bell, Ronald Komar, William B. Chodirker

Journal:

Seminars in Arthritis and Rheumatism

Year:

1989

Language:

english

File:

PDF, 2.35 MB

english, 1989

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