Chodirker BN - Search Results

1

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

Greenberg CR, Evans JA, McKendry-Smith S, Redekopp S, Haworth JC, Mulivor R, Chodirker BN. Greenberg CR, et al. Among authors: chodirker bn. Am J Hum Genet. 1990 Feb;46(2):286-92. Am J Hum Genet. 1990. PMID: 1689104 Free PMC article.

2

Paracentric inversion 11q in Canadian Hutterites.

Chodirker BN, Greenberg CR, Pabello PD, Chudley AE. Chodirker BN, et al. Hum Genet. 1992 Jun;89(4):450-2. doi: 10.1007/BF00194321. Hum Genet. 1992. PMID: 1618494

3

Hyperphosphatemia in infantile hypophosphatasia: implications for carrier diagnosis and screening.

Chodirker BN, Evans JA, Seargeant LE, Cheang MS, Greenberg CR. Chodirker BN, et al. Am J Hum Genet. 1990 Feb;46(2):280-5. Am J Hum Genet. 1990. PMID: 2301398 Free PMC article.

4

Infantile hypophosphatasia--linkage with the RH locus.

Chodirker BN, Evans JA, Lewis M, Coghlan G, Belcher E, Philipps S, Seargeant LE, Sus C, Greenberg CR. Chodirker BN, et al. Genomics. 1987 Nov;1(3):280-2. doi: 10.1016/0888-7543(87)90056-5. Genomics. 1987. PMID: 3128473

5

Computer assisted analysis of hand radiographs in infantile hypophosphatasia carriers.

Chodirker BN, Roy D, Greenberg CR, Cheang M, Evans JA, Reed MH. Chodirker BN, et al. Pediatr Radiol. 1991;21(3):216-9. doi: 10.1007/BF02011052. Pediatr Radiol. 1991. PMID: 2047163

6

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

Chodirker BN, Coburn SP, Seargeant LE, Whyte MP, Greenberg CR. Chodirker BN, et al. J Inherit Metab Dis. 1990;13(6):891-6. doi: 10.1007/BF01800216. J Inherit Metab Dis. 1990. PMID: 2079838

7

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

Chodirker BN, Harman CR, Greenberg CR. Chodirker BN, et al. Prenat Diagn. 1988 May;8(4):291-6. doi: 10.1002/pd.1970080408. Prenat Diagn. 1988. PMID: 3041404

8

Elevated MSAFP levels and congenital heart defects: lack of an association.

Albar H, MacDonald KM, Harman CR, Evans JA, Chodirker BN. Albar H, et al. Among authors: chodirker bn. Am J Med Genet. 1994 Feb 1;49(3):337-40. doi: 10.1002/ajmg.1320490319. Am J Med Genet. 1994. PMID: 7516120

9

Evidence for Ritscher-Schinzel syndrome in Canadian Native Indians.

Marles SL, Chodirker BN, Greenberg CR, Chudley AE. Marles SL, et al. Among authors: chodirker bn. Am J Med Genet. 1995 May 8;56(4):343-50. doi: 10.1002/ajmg.1320560402. Am J Med Genet. 1995. PMID: 7604842 Review.

10

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

Gorski SM, Adams KJ, Birch PH, Chodirker BN, Greenberg CR, Goodfellow PJ. Gorski SM, et al. Among authors: chodirker bn. Hum Genet. 1994 Aug;94(2):141-8. doi: 10.1007/BF00202859. Hum Genet. 1994. PMID: 8045560

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