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mitchell innes a[Author]
(26 results)?
Expansion of the GLE1-associated arthrogryposis multiplex congenita clinical spectrum.
Clin Genet. 2017 Mar;91(3):426-430. doi: 10.1111/cge.12876. Epub 2017 Jan 30.
Clin Genet. 2017.
PMID: 27684565
Refinement of the critical region of 1q41q42 microdeletion syndrome identifies FBXO28 as a candidate causative gene for intellectual disability and seizures.
Au PY, Argiropoulos B, Parboosingh JS, Micheil Innes A.
Au PY, et al. Among authors: micheil innes a.
Am J Med Genet A. 2014 Feb;164A(2):441-8. doi: 10.1002/ajmg.a.36320. Epub 2013 Dec 19.
Am J Med Genet A. 2014.
PMID: 24357076
Review.
Item in Clipboard
Prenatal features of Costello syndrome: ultrasonographic findings and atrial tachycardia.
Lin AE, O'Brien B, Demmer LA, Almeda KK, Blanco CL, Glasow PF, Berul CI, Hamilton R, Micheil Innes A, Lauzon JL, Sol-Church K, Gripp KW.
Lin AE, et al. Among authors: micheil innes a.
Prenat Diagn. 2009 Jul;29(7):682-90. doi: 10.1002/pd.2276.
Prenat Diagn. 2009.
PMID: 19382114
Free PMC article.
Item in Clipboard
Interstitial deletion of 11q in a mother and fetus: implications of directly transmitted chromosomal imbalances for prenatal genetic counseling.
Sparkes RL, Shetty S, Chernos JE, Mefford HC, Micheil Innes A.
Sparkes RL, et al. Among authors: micheil innes a.
Prenat Diagn. 2009 Mar;29(3):283-6. doi: 10.1002/pd.2209.
Prenat Diagn. 2009.
PMID: 19177486
No abstract available.
Item in Clipboard
High frequency of copy number variations (CNVs) in the chromosome 11p15 region in patients with Beckwith-Wiedemann syndrome.
Baskin B, Choufani S, Chen YA, Shuman C, Parkinson N, Lemyre E, Micheil Innes A, Stavropoulos DJ, Ray PN, Weksberg R.
Baskin B, et al. Among authors: micheil innes a.
Hum Genet. 2014 Mar;133(3):321-30. doi: 10.1007/s00439-013-1379-z. Epub 2013 Oct 24.
Hum Genet. 2014.
PMID: 24154661
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Re: 3C (Ritscher-Schinzel) syndrome: the importance of ruling out a terminal 6p deletion.
Micheil Innes A.
Micheil Innes A.
Clin Dysmorphol. 2005 Oct;14(4):209-210.
Clin Dysmorphol. 2005.
PMID: 16155425
No abstract available.
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