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Recurrent spontaneous pregnancy loss. Investigation and reproductive follow-up.
J Reprod Med. 1991 Mar;36(3):184-8.
J Reprod Med. 1991.
PMID: 2030494
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.
BMC Med Genet. 2014 Jul 16;15:82. doi: 10.1186/1471-2350-15-82.
BMC Med Genet. 2014.
PMID: 25030379
Free PMC article.
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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: hurlburt j.
Mol Cytogenet. 2008 Nov 11;1:23. doi: 10.1186/1755-8166-1-23.
Mol Cytogenet. 2008.
PMID: 19000322
Free PMC article.
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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.
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.
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Characterization of a new X-linked mental retardation syndrome with microcephaly, cortical malformation, and thin habitus.
du Souich C, Chou A, Yin J, Oh T, Nelson TN, Hurlburt J, Arbour L, Friedlander R, McGillivray BC, Tyshchenko N, Rump A, Poskitt KJ, Demos MK, Van Allen MI, Boerkoel CF.
du Souich C, et al.
Am J Med Genet A. 2009 Nov;149A(11):2469-78. doi: 10.1002/ajmg.a.33071.
Am J Med Genet A. 2009.
PMID: 19842190
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Hypomorphic temperature-sensitive alleles of NSDHL cause CK syndrome.
McLarren KW, Severson TM, du Souich C, Stockton DW, Kratz LE, Cunningham D, Hendson G, Morin RD, Wu D, Paul JE, An J, Nelson TN, Chou A, DeBarber AE, Merkens LS, Michaud JL, Waters PJ, Yin J, McGillivray B, Demos M, Rouleau GA, Grzeschik KH, Smith R, Tarpey PS, Shears D, Schwartz CE, Gecz J, Stratton MR, Arbour L, Hurlburt J, Van Allen MI, Herman GE, Zhao Y, Moore R, Kelley RI, Jones SJ, Steiner RD, Raymond FL, Marra MA, Boerkoel CF.
McLarren KW, et al.
Am J Hum Genet. 2010 Dec 10;87(6):905-14. doi: 10.1016/j.ajhg.2010.11.004.
Am J Hum Genet. 2010.
PMID: 21129721
Free PMC article.
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Germline BRCA1 and BRCA2 mutations in ovarian cancer: utility of a histology-based referral strategy.
Schrader KA, Hurlburt J, Kalloger SE, Hansford S, Young S, Huntsman DG, Gilks CB, McAlpine JN.
Schrader KA, et al.
Obstet Gynecol. 2012 Aug;120(2 Pt 1):235-40. doi: 10.1097/AOG.0b013e31825f3576.
Obstet Gynecol. 2012.
PMID: 22776961
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Intravaginal rings as delivery systems for microbicides and multipurpose prevention technologies.
Thurman AR, Clark MR, Hurlburt JA, Doncel GF.
Thurman AR, et al. Among authors: hurlburt ja.
Int J Womens Health. 2013 Oct 21;5:695-708. doi: 10.2147/IJWH.S34030.
Int J Womens Health. 2013.
PMID: 24174884
Free PMC article.
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