McGillivray B - Search Results

1

Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1.

Rajcan-Separovic E, Harvard C, Liu X, McGillivray B, Hall JG, Qiao Y, Hurlburt J, Hildebrand J, Mickelson EC, Holden JJ, Lewis ME. Rajcan-Separovic E, et al. Among authors: mcgillivray b. J Med Genet. 2007 Apr;44(4):269-76. doi: 10.1136/jmg.2006.045013. Epub 2006 Sep 8. J Med Genet. 2007. PMID: 16963482 Free PMC article.

2

Molecular cytogenetic investigation of two patients with Y chromosome rearrangements and intellectual disability.

Tyson C, Dawson AJ, Bal S, Tomiuk M, Anderson T, Tucker D, Riordan D, Chudoba I, Morash B, Mhanni A, Chudley AE, McGillivray B, Parslow M, Rappold G, Roeth R, Fawcett C, Qiao Y, Harvard C, Rajcan-Separovic E. Tyson C, et al. Among authors: mcgillivray b. Am J Med Genet A. 2009 Mar;149A(3):490-5. doi: 10.1002/ajmg.a.32535. Am J Med Genet A. 2009. PMID: 19213034

3

Elucidation of a cryptic interstitial 7q31.3 deletion in a patient with a language disorder and mild mental retardation by array-CGH.

Tyson C, McGillivray B, Chijiwa C, Rajcan-Separovic E. Tyson C, et al. Among authors: mcgillivray b. Am J Med Genet A. 2004 Sep 1;129A(3):254-60. doi: 10.1002/ajmg.a.30245. Am J Med Genet A. 2004. PMID: 15326624

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

Copy number variants (CNVs) analysis in a deeply phenotyped cohort of individuals with intellectual disability (ID).

Qiao Y, Mercier E, Dastan J, Hurlburt J, McGillivray B, Chudley AE, Farrell S, Bernier FP, Lewis MS, Pavlidis P, Rajcan-Separovic E. Qiao Y, et al. Among authors: mcgillivray b. BMC Med Genet. 2014 Jul 16;15:82. doi: 10.1186/1471-2350-15-82. BMC Med Genet. 2014. PMID: 25030379 Free PMC article.

6

Normal male carriers in the fra(X) form of X-linked mental retardation (Martin-Bell syndrome).

Froster-Iskenius U, McGillivray BC, Dill FJ, Hall JG, Herbst DS. Froster-Iskenius U, et al. Among authors: mcgillivray bc. Am J Med Genet. 1986 Jan-Feb;23(1-2):619-31. doi: 10.1002/ajmg.1320230156. Am J Med Genet. 1986. PMID: 3953672

7

Bleeding diathesis in Noonan syndrome: a common association.

Witt DR, McGillivray BC, Allanson JE, Hughes HE, Hathaway WE, Zipursky A, Hall JG. Witt DR, et al. Among authors: mcgillivray bc. Am J Med Genet. 1988 Oct;31(2):305-17. doi: 10.1002/ajmg.1320310208. Am J Med Genet. 1988. PMID: 3232698

8

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

9

Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGH.

Tyson C, Qiao Y, Harvard C, Liu X, Bernier FP, McGillivray B, Farrell SA, Arbour L, Chudley AE, Clarke L, Gibson W, Dyack S, McLeod R, Costa T, Vanallen MI, Yong SL, Graham GE, Macleod P, Patel MS, Hurlburt J, Holden JJ, Lewis SM, Rajcan-Separovic E. Tyson C, et al. Among authors: mcgillivray b. Mol Cytogenet. 2008 Nov 11;1:23. doi: 10.1186/1755-8166-1-23. Mol Cytogenet. 2008. PMID: 19000322 Free PMC article.

10

Segregation analysis of microcephaly.

Cohen T, Zeitune M, McGillivray BC, Hall JG, Lynn AH, Aston CE, Chakravarti A. Cohen T, et al. Among authors: mcgillivray bc. Am J Med Genet. 1996 Oct 28;65(3):226-34. doi: 10.1002/(SICI)1096-8628(19961028)65:3<226::AID-AJMG11>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 9240749

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