B.N. Chodirker

Infantile hypophosphatasia: localization within chromosome region 1p36.1-34 and prenatal diagnosis using linked DNA markers.

Cheryl R. Greenberg, Jane Evans, S McKendry-Smith et al. · PubMed · 1990 · 113 citations

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 · 1995 · 49 citations

Early Diagnosis, Guthrie Blood Spots, Neonatology +9

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 et al. · Journal of Inherited Metabolic Disease · 1989 · 42 citations

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

B.N. Chodirker, Chris Harman, Cheryl R. Greenberg · Prenatal Diagnosis · 1988 · 37 citations

Developmental Anomaly, Healthy Baby, Mendelian Disorder +13

Bowen–Conradi syndrome: A clinical and genetic study

R. Brian Lowry, A. Micheil Innes, François P. Bernier et al. · American Journal of Medical Genetics Part A · 2003 · 32 citations

Family Medicine, Mendelian Disorder, Genetic Disorder +10