McGillivray BC - Search Results

1

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

2

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. Prenat Diagn. 2006 Apr;26(4):324-9. doi: 10.1002/pd.1406. Prenat Diagn. 2006. PMID: 16521154 Review.

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

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

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. Prenat Diagn. 2002 May;22(5):388-94. doi: 10.1002/pd.319. Prenat Diagn. 2002. PMID: 12001193

6

Spontaneous abortion and pregnancy outcome after normal first-trimester ultrasound examination.

Wilson RD, Kendrick V, Wittmann BK, McGillivray B. Wilson RD, et al. Obstet Gynecol. 1986 Mar;67(3):352-5. Obstet Gynecol. 1986. PMID: 3511418

7

Familial renal hypophosphatemia, minor facial anomalies, intracerebral calcifications, and non-rachitic bone changes: apparently new syndrome?

Chitayat D, McGillivray BC, Rothstein R, Flodmark O, Priddy RW, Ebelt VJ, Lirenman DS, Hall JG. Chitayat D, et al. Among authors: mcgillivray bc. Am J Med Genet. 1990 Mar;35(3):406-14. doi: 10.1002/ajmg.1320350318. Am J Med Genet. 1990. PMID: 2309790

8

Interstitial 7q deletion [46,XX,del(7)(pter----q21.1::q22----qter)] and the location of genes for beta-glucuronidase and cystic fibrosis.

Chitayat D, McGillivray BC, Wood S, Kalousek DK, Langlois S, Applegarth DA. Chitayat D, et al. Among authors: mcgillivray bc. Am J Med Genet. 1988 Nov;31(3):655-61. doi: 10.1002/ajmg.1320310321. Am J Med Genet. 1988. PMID: 3228144

9

Prenatally detected trisomy 20 mosaicism.

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

10

Evidence for multi-site closure of the neural tube in humans.

Van Allen MI, Kalousek DK, Chernoff GF, Juriloff D, Harris M, McGillivray BC, Yong SL, Langlois S, MacLeod PM, Chitayat D, et al. Van Allen MI, et al. Among authors: mcgillivray bc. Am J Med Genet. 1993 Oct 1;47(5):723-43. doi: 10.1002/ajmg.1320470528. Am J Med Genet. 1993. PMID: 8267004 Review.

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