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A chromosomal deletion map of human malformations.
Brewer C, Holloway S, Zawalnyski P, Schinzel A, FitzPatrick D. Brewer C, et al. Among authors: schinzel a. Am J Hum Genet. 1998 Oct;63(4):1153-9. doi: 10.1086/302041. Am J Hum Genet. 1998. PMID: 9758599 Free PMC article.
Chromosomal map of human brain malformations.
Tyshchenko N, Lurie I, Schinzel A. Tyshchenko N, et al. Among authors: schinzel a. Hum Genet. 2008 Aug;124(1):73-80. doi: 10.1007/s00439-008-0528-2. Epub 2008 Jun 18. Hum Genet. 2008. PMID: 18563447 Free article.
Nondisjunction of chromosome 15: origin and recombination.
Robinson WP, Bernasconi F, Mutirangura A, Ledbetter DH, Langlois S, Malcolm S, Morris MA, Schinzel AA. Robinson WP, et al. Among authors: schinzel aa. Am J Hum Genet. 1993 Sep;53(3):740-51. Am J Hum Genet. 1993. PMID: 8352279 Free PMC article.
Chromosome imbalances associated with epilepsy.
Schinzel A, Niedrist D. Schinzel A, et al. Am J Med Genet. 2001 Summer;106(2):119-24. doi: 10.1002/ajmg.1576. Am J Med Genet. 2001. PMID: 11579431 Review.
BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defects.
Hilton E, Johnston J, Whalen S, Okamoto N, Hatsukawa Y, Nishio J, Kohara H, Hirano Y, Mizuno S, Torii C, Kosaki K, Manouvrier S, Boute O, Perveen R, Law C, Moore A, Fitzpatrick D, Lemke J, Fellmann F, Debray FG, Dastot-Le-Moal F, Gerard M, Martin J, Bitoun P, Goossens M, Verloes A, Schinzel A, Bartholdi D, Bardakjian T, Hay B, Jenny K, Johnston K, Lyons M, Belmont JW, Biesecker LG, Giurgea I, Black G. Hilton E, et al. Among authors: schinzel a. Eur J Hum Genet. 2009 Oct;17(10):1325-35. doi: 10.1038/ejhg.2009.52. Epub 2009 Apr 15. Eur J Hum Genet. 2009. PMID: 19367324 Free PMC article.
414 results