McGillivray B - Search Results

1

Isodicentric Yp: prenatal diagnosis and outcome in 12 cases.

Bruyère H, Speevak MD, Winsor EJ, de Fréminville B, Farrell SA, McGowan-Jordan J, McGillivray B, Chitayat D, McFadden D, Adouard V, Terespolsky D, Prieur F, Pantzar T, Hrynchak M. Bruyère H, et al. Among authors: mcgillivray b. Prenat Diagn. 2006 Apr;26(4):324-9. doi: 10.1002/pd.1406. Prenat Diagn. 2006. PMID: 16521154 Review.

2

Role of prenatal detection of cardiac tumours in the diagnosis of tuberous sclerosis--report of two cases.

Chitayat D, McGillivray BC, Diamant S, Wittmann BK, Sandor GG. Chitayat D, et al. Among authors: mcgillivray bc. Prenat Diagn. 1988 Oct;8(8):577-84. doi: 10.1002/pd.1970080805. Prenat Diagn. 1988. PMID: 3060871

3

Fetal ultrasound abnormalities: correlation with fetal karyotype, autopsy findings, and postnatal outcome--five-year prospective study.

Wilson RD, Chitayat D, McGillivray BC. Wilson RD, et al. Among authors: mcgillivray bc. Am J Med Genet. 1992 Nov 15;44(5):586-90. doi: 10.1002/ajmg.1320440511. Am J Med Genet. 1992. PMID: 1481814

4

Confined chorionic mosaicism in prenatal diagnosis.

Kalousek DK, Dill FJ, Pantzar T, McGillivray BC, Yong SL, Wilson RD. Kalousek DK, et al. Among authors: mcgillivray bc. Hum Genet. 1987 Oct;77(2):163-7. doi: 10.1007/BF00272385. Hum Genet. 1987. PMID: 3653890

5

Prenatal diagnosis of apparently isolated unilateral multicystic kidney: implications for counselling and management.

Aubertin G, Cripps S, Coleman G, McGillivray B, Yong SL, Van Allen M, Shaw D, Arbour L. Aubertin G, et al. Among authors: mcgillivray b. Prenat Diagn. 2002 May;22(5):388-94. doi: 10.1002/pd.319. Prenat Diagn. 2002. PMID: 12001193

6

Prenatally detected trisomy 20 mosaicism.

Robinson WP, McGillivray B, Lewis ME, Arbour L, Barrett I, Kalousek DK. Robinson WP, et al. Among authors: mcgillivray b. Prenat Diagn. 2005 Mar;25(3):239-44. doi: 10.1002/pd.1121. Prenat Diagn. 2005. PMID: 15791659

7

Pregnancy and postnatal outcome of mosaic isochromosome 20q.

Robinson WP, McGillivray B, Friedman JM. Robinson WP, et al. Among authors: mcgillivray b. Prenat Diagn. 2007 Feb;27(2):143-5. doi: 10.1002/pd.1636. Prenat Diagn. 2007. PMID: 17191261

8

Perinatal and first year follow-up of patients with Prader-Willi syndrome: normal size of hands and feet.

Chitayat D, Davis EB, McGillivray BC, Hayden MR, Hall JG. Chitayat D, et al. Among authors: mcgillivray bc. Clin Genet. 1989 Mar;35(3):161-6. doi: 10.1111/j.1399-0004.1989.tb02923.x. Clin Genet. 1989. PMID: 2706799

9

Familial 5q11.2----q13.3 segmental duplication cosegregating with multiple anomalies, including schizophrenia.

McGillivray BC, Bassett AS, Langlois S, Pantzar T, Wood S. McGillivray BC, et al. Am J Med Genet. 1990 Jan;35(1):10-3. doi: 10.1002/ajmg.1320350103. Am J Med Genet. 1990. PMID: 1967903 Free PMC article.

10

BPES with atypical premature ovarian insufficiency, and evidence of mitotic recombination, in a woman with trisomy X and a translocation t(3;11)(q22.3;q14.1).

Schlade-Bartusiak K, Brown L, Lomax B, Bruyère H, Gillan T, Hamilton S, McGillivray B, Eydoux P. Schlade-Bartusiak K, et al. Among authors: mcgillivray b. Am J Med Genet A. 2012 Sep;158A(9):2322-7. doi: 10.1002/ajmg.a.35516. Epub 2012 Aug 6. Am J Med Genet A. 2012. PMID: 22887799

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