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Perinatal follow-up of children born after preimplantation genetic diagnosis between 1995 and 2014.
Heijligers M, van Montfoort A, Meijer-Hoogeveen M, Broekmans F, Bouman K, Homminga I, Dreesen J, Paulussen A, Engelen J, Coonen E, van der Schoot V, van Deursen-Luijten M, Muntjewerff N, Peeters A, van Golde R, van der Hoeven M, Arens Y, de Die-Smulders C. Heijligers M, et al. Among authors: engelen j. J Assist Reprod Genet. 2018 Nov;35(11):1995-2002. doi: 10.1007/s10815-018-1286-2. Epub 2018 Sep 5. J Assist Reprod Genet. 2018. PMID: 30187425 Free PMC article.
Prader-Willi-like phenotype in fragile X syndrome.
Schrander-Stumpel C, Gerver WJ, Meyer H, Engelen J, Mulder H, Fryns JP. Schrander-Stumpel C, et al. Among authors: engelen j. Clin Genet. 1994 Apr;45(4):175-80. doi: 10.1111/j.1399-0004.1994.tb04018.x. Clin Genet. 1994. PMID: 8062434
Trisomy 7p: report of 2 patients and literature review.
Arens YH, Toutain A, Engelen JJ, Offermans JP, Hamers AJ, Schrander JJ, Pulles-Heintzberger CF, Schrander-Stumpel CT. Arens YH, et al. Among authors: engelen jj. Genet Couns. 2000;11(4):347-54. Genet Couns. 2000. PMID: 11140412 Review.
Subtelomeric chromosome aberrations: still a lot to learn.
Moog U, Arens YH, van Lent-Albrechts JC, Huijts PE, Smeets EE, Schrander-Stumpel CT, Engelen JJ. Moog U, et al. Among authors: engelen jj. Clin Genet. 2005 Nov;68(5):397-407. doi: 10.1111/j.1399-0004.2005.00506.x. Clin Genet. 2005. PMID: 16207207
Marker chromosome identification by micro-FISH.
Engelen JJ, Loots WJ, Motoh PC, Moog U, Hamers GJ, Geraedts JP. Engelen JJ, et al. Clin Genet. 1996 May;49(5):242-8. doi: 10.1111/j.1399-0004.1996.tb03781.x. Clin Genet. 1996. PMID: 8832132
Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion.
Poelmans G, Engelen JJ, Van Lent-Albrechts J, Smeets HJ, Schoenmakers E, Franke B, Buitelaar JK, Wuisman-Frerker M, Erens W, Steyaert J, Schrander-Stumpel C. Poelmans G, et al. Among authors: engelen jj. Am J Med Genet B Neuropsychiatr Genet. 2009 Jan 5;150B(1):140-7. doi: 10.1002/ajmg.b.30787. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 18521840
176 results