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stankovich m[au]
(58 results)?
The role of FREM2 and FRAS1 in the development of congenital diaphragmatic hernia.
Hum Mol Genet. 2018 Jun 15;27(12):2064-2075. doi: 10.1093/hmg/ddy110.
Hum Mol Genet. 2018.
PMID: 29618029
Free PMC article.
Chromosome 5q33 deletions associated with congenital heart defects.
Starkovich M, Lalani SR, Mercer CL, Scott DA.
Starkovich M, et al.
Am J Med Genet A. 2016 Dec;170(12):3338-3342. doi: 10.1002/ajmg.a.37957. Epub 2016 Sep 2.
Am J Med Genet A. 2016.
PMID: 27589475
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Congenital heart defects and left ventricular non-compaction in males with loss-of-function variants in NONO.
Scott DA, Hernandez-Garcia A, Azamian MS, Jordan VK, Kim BJ, Starkovich M, Zhang J, Wong LJ, Darilek SA, Breman AM, Yang Y, Lupski JR, Jiwani AK, Das B, Lalani SR, Iglesias AD, Rosenfeld JA, Xia F.
Scott DA, et al. Among authors: starkovich m.
J Med Genet. 2017 Jan;54(1):47-53. doi: 10.1136/jmedgenet-2016-104039. Epub 2016 Aug 22.
J Med Genet. 2017.
PMID: 27550220
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Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability.
Grau C, Starkovich M, Azamian MS, Xia F, Cheung SW, Evans P, Henderson A, Lalani SR, Scott DA.
Grau C, et al. Among authors: starkovich m.
PLoS One. 2017 Apr 17;12(4):e0175962. doi: 10.1371/journal.pone.0175962. eCollection 2017.
PLoS One. 2017.
PMID: 28414775
Free PMC article.
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