B.N. Chodirker - Concepedia

Author

B.N. Chodirker

University of Manitoba

Also Known As

B Chodirker, B N Chodirker, B. Chodirker, B. N. Chodirker, B.N. Chodirker, BernardN. Chodirker

Publications

459

Citations

H-Index

Concepts

All Affiliations

University of Manitoba Children's Hospital of Winnipeg Health Sciences Centre

About

B.N. Chodirker is an author at University of Manitoba specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	177
2	Biology	2	2	54
3	Engineering	1	1	10
4	Natural Sciences	1	1	22
5	Family Medicine	1	1	32

B.N. Chodirker

Publications

434

Citations

H-Index

Page 1

	Year	Citations
Infantile hypophosphatasia: localization within chromosome region 1p36.1-34 and prenatal diagnosis using linked DNA markers. Cheryl R. Greenberg, Jane Evans, S McKendry-Smith, PubMed	1990	113
Frequency of FMR1 Premutations in a Consecutive Newborn Population by PCR Screening of Guthrie Blood Spots AJ Dawson, B.N. Chodirker, Albert E. Chudley Biochemical and Molecular Medicine Early DiagnosisGuthrie Blood SpotsNeonatologyFmr1 PremutationsPcr Screening	1995	49
Increased plasma pyridoxal‐5′‐phosphate levels before and after pyridoxine loading in carriers of perinatal/infantile hypophosphatasia B.N. Chodirker, Stephen P. Coburn, L.E. Seargeant, Journal of Inherited Metabolic Disease	1989	42
Spontaneous resolution of a cystic hygroma in a fetus with Turner syndrome B.N. Chodirker, Chris Harman, Cheryl R. Greenberg Prenatal Diagnosis Developmental AnomalyHealthy BabyMendelian DisorderCystic HygromaGenetic Disorder	1988	37
Bowen–Conradi syndrome: A clinical and genetic study R. Brian Lowry, A. Micheil Innes, François P. Bernier, American Journal of Medical Genetics Part A Family MedicineMendelian DisorderGenetic DisorderKinship CoefficientsGenetic Epidemiology	2003	32
Infantile hypophosphatasia—Linkage with the RH locus B.N. Chodirker, Jane Evans, M. Lewis, Genomics BiologyRh LocusGenetic DisorderGeneticsAbnormal Development	1987	32
Hyperphosphatemia in infantile hypophosphatasia: implications for carrier diagnosis and screening. B.N. Chodirker, Jane Evans, L.E. Seargeant, PubMed	1990	30
Fragile 19p13 in a family with mental illness B.N. Chodirker, Albert E. Chudley, M. Ray, Clinical Genetics	1987	30
Linkage analysis of X-linked cleft palate and ankyloglossia in Manitoba Mennonite and British Columbia Native kindreds Sharon M. Gorski, KarenJ. Adams, Patricia Birch, Human Genetics BiologyMorphological EvidenceNatural SciencesGeneticsEvolutionary Biology	1994	22
Refinement of the hereditary xerocytosis locus on chromosome 16q in a large Canadian kindred Brett L. Houston, Teresa Zelinski, Sara J. Israels, Blood Cells Molecules and Diseases ChromatinMendelian DisorderCytogeneticsGenetic DisorderGenetics	2011	22

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