Chodirker BN - Search Results

1

Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in Canada.

Armour CM, Dougan SD, Brock JA, Chari R, Chodirker BN, DeBie I, Evans JA, Gibson WT, Kolomietz E, Nelson TN, Tihy F, Thomas MA, Stavropoulos DJ; On-Behalf-Of the Canadian College of Medical Geneticists. Armour CM, et al. Among authors: chodirker bn. J Med Genet. 2018 Apr;55(4):215-221. doi: 10.1136/jmedgenet-2017-105013. Epub 2018 Mar 1. J Med Genet. 2018. PMID: 29496978 Free PMC article.

2

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

3

Severe acro-renal-uterine-mandibular syndrome.

Evans JA, Phillips S, Reed M, Chodirker BN. Evans JA, et al. Among authors: chodirker bn. Am J Med Genet. 2000 Jul 3;93(1):67-73. doi: 10.1002/1096-8628(20000703)93:1<67::aid-ajmg11>3.0.co;2-k. Am J Med Genet. 2000. PMID: 10861684

4

Proposed guideline for fetal choroid plexus cysts.

Chodirker BN, Evans JA, McRae AR. Chodirker BN, et al. J Obstet Gynaecol Can. 2006 Oct;28(10):865-866. doi: 10.1016/S1701-2163(16)32271-X. J Obstet Gynaecol Can. 2006. PMID: 17140500 No abstract available.

5

Low MSAFP levels and Williams syndrome.

Chodirker BN, Greenberg CR, Giddins NG, Dawson AJ, Evans JA, Chudley AE. Chodirker BN, et al. Am J Med Genet. 1997 Nov 12;72(4):448-50. doi: 10.1002/(sici)1096-8628(19971112)72:4<448::aid-ajmg14>3.0.co;2-r. Am J Med Genet. 1997. PMID: 9375729

6

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

Evans JA, Chodirker BN. Evans JA, et al. Among authors: chodirker bn. Am J Med Genet. 1993 Aug 1;47(1):112-3. doi: 10.1002/ajmg.1320470123. Am J Med Genet. 1993. PMID: 8240537 No abstract available.

7

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

Bamforth JS, Leonard CO, Chodirker BN, Chitayat D, Gritter HL, Evans JA, Keena B, Pantzar T, Friedman JM, Hall JG. Bamforth JS, et al. Among authors: chodirker bn. Am J Med Genet. 1989 Jan;32(1):93-9. doi: 10.1002/ajmg.1320320120. Am J Med Genet. 1989. PMID: 2650550

8

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.

9

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.

10

MSAFP levels and oesophageal atresia.

Chodirker BN, Chudley AE, MacDonald KM, Harman CR, Evans JA. Chodirker BN, et al. Prenat Diagn. 1994 Nov;14(11):1086-9. doi: 10.1002/pd.1970141114. Prenat Diagn. 1994. PMID: 7533286

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