Chernos J[au] - Search Results

Year	Number of Results
1986	1
1989	1
1990	1
1991	1
1992	2
1993	1
1994	1
1997	1
1999	1
2000	2
2001	1
2002	2
2003	2
2004	1
2005	3
2007	2
2008	3
2009	2
2010	2
2011	4
2012	1
2013	2
2014	2
2016	2
2017	1
2018	1
2019	1
2021	1
2024	0

1

Review of the recurrent 8q13.2q13.3 branchio-oto-renal related microdeletion, and report of an additional case with associated distal arthrogryposis.

Au PB, Chernos JE, Thomas MA. Au PB, et al. Among authors: chernos je. Am J Med Genet A. 2016 Nov;170(11):2984-2987. doi: 10.1002/ajmg.a.37695. Epub 2016 Aug 19. Am J Med Genet A. 2016. PMID: 27542115 Review.

2

Characterization of an interstitial deletion del(13)(q22q32) using microdissection and sequential FISH and G-banding.

Xu J, Chernos JE, Bernier F, Lowry RB. Xu J, et al. Among authors: chernos je. Genet Test. 2000;4(3):279-82. doi: 10.1089/10906570050501506. Genet Test. 2000. PMID: 11142759 Review.

3

Aneuploid spermatozoa in infertile men: teratozoospermia.

Templado C, Hoang T, Greene C, Rademaker A, Chernos J, Martin R. Templado C, et al. Among authors: chernos j. Mol Reprod Dev. 2002 Feb;61(2):200-4. doi: 10.1002/mrd.1148. Mol Reprod Dev. 2002. PMID: 11803555

4

Epithelial cells in PBSC grafts: source of donor-type epithelial cells after allogeneic transplantation?

Khan FM, Sy S, Louie P, Smith M, Chernos J, Russell JA, Storek J. Khan FM, et al. Among authors: chernos j. Bone Marrow Transplant. 2012 Mar;47(3):461-2. doi: 10.1038/bmt.2011.100. Epub 2011 May 23. Bone Marrow Transplant. 2012. PMID: 21602896 No abstract available.

5

CCMG guidelines: prenatal and postnatal diagnostic testing for uniparental disomy.

Dawson AJ, Chernos J, McGowan-Jordan J, Lavoie J, Shetty S, Steinraths M, Wang JC, Xu J; Canadian College of Medical Geneticists committees. Dawson AJ, et al. Among authors: chernos j. Clin Genet. 2011 Feb;79(2):118-24. doi: 10.1111/j.1399-0004.2010.01547.x. Epub 2010 Oct 12. Clin Genet. 2011. PMID: 21039433

6

Microduplication and triplication of 22q11.2: a highly variable syndrome.

Yobb TM, Somerville MJ, Willatt L, Firth HV, Harrison K, MacKenzie J, Gallo N, Morrow BE, Shaffer LG, Babcock M, Chernos J, Bernier F, Sprysak K, Christiansen J, Haase S, Elyas B, Lilley M, Bamforth S, McDermid HE. Yobb TM, et al. Among authors: chernos j. Am J Hum Genet. 2005 May;76(5):865-76. doi: 10.1086/429841. Epub 2005 Mar 30. Am J Hum Genet. 2005. PMID: 15800846 Free PMC article.

7

Clinical and molecular characterization of an almost complete ring chromosome 4 in two sisters, with recurrence due to gonadal mosaicism.

Phillips EA, Caluseriu O, Schlade-Bartusiak K, Chernos J, McLeod DR, Thomas MA. Phillips EA, et al. Among authors: chernos j. Clin Dysmorphol. 2021 Oct 1;30(4):173-176. doi: 10.1097/MCD.0000000000000382. Clin Dysmorphol. 2021. PMID: 34417371

8

Prenatal Array Comparative Genomic Hybridization in Fetuses With Structural Cardiac Anomalies.

Lazier J, Fruitman D, Lauzon J, Bernier F, Argiropoulos B, Chernos J, Caluseriu O, Simrose R, Thomas MA. Lazier J, et al. Among authors: chernos j. J Obstet Gynaecol Can. 2016 Jul;38(7):619-26. doi: 10.1016/j.jogc.2016.02.010. Epub 2016 May 6. J Obstet Gynaecol Can. 2016. PMID: 27591345

9

A 2q24.3q31.1 microdeletion found in a patient with Filippi-like syndrome phenotype: a case report.

Lazier J, Chernos J, Lowry RB. Lazier J, et al. Among authors: chernos j. Am J Med Genet A. 2014 Sep;164A(9):2385-7. doi: 10.1002/ajmg.a.36636. Epub 2014 Jun 12. Am J Med Genet A. 2014. PMID: 24924433

10

Interstitial deletions at 6q14.1q15 associated with developmental delay and a marfanoid phenotype.

Lowry RB, Chernos JE, Connelly MS, Wyse JP. Lowry RB, et al. Among authors: chernos je. Mol Syndromol. 2013 Sep;4(6):280-4. doi: 10.1159/000354038. Epub 2013 Aug 1. Mol Syndromol. 2013. PMID: 24167463 Free PMC article.

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