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Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion.
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
Familial insertion (3;5)(q25.3;q22.1q31.3) with deletion or duplication of chromosome region 5q22.1-5q31.3 in ten unbalanced carriers.
Arens YH, Engelen JJ, Govaerts LC, van Ravenswaay CM, Loneus WH, van Lent-Albrechts JC, van der Blij-Philipsen M, Hamers AJ, Schrander-Stumpel CT.
Arens YH, et al. Among authors: van lent albrechts jc.
Am J Med Genet A. 2004 Oct 1;130A(2):128-33. doi: 10.1002/ajmg.a.20568.
Am J Med Genet A. 2004.
PMID: 15372532
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Sonographic genital ambiguity in a fetus due to a mosaic 45,X/46,X,idic(Y)(qter-p11.32::p11.32-qter) karyotype.
Marcus-Soekarman D, Hamers G, Mulder AL, Offermans J, Offermans J, Engelen J, van Lent-Albrechts JC, Robben SG, de Muinck Keizer-Schrama S, Wolffenbuttel KP, Looijenga LH, Oosterhuis JW, Schrander-Stumpel C, Nijhuis J.
Marcus-Soekarman D, et al. Among authors: van lent albrechts jc.
Prenat Diagn. 2005 Apr;25(4):279-82. doi: 10.1002/pd.996.
Prenat Diagn. 2005.
PMID: 15849784
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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: van lent albrechts jc.
Clin Genet. 2005 Nov;68(5):397-407. doi: 10.1111/j.1399-0004.2005.00506.x.
Clin Genet. 2005.
PMID: 16207207
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All-in-one whole exome sequencing strategy with simultaneous copy number variant, single nucleotide variant and absence-of-heterozygosity analysis in fetuses with structural ultrasound anomalies: A 1-year experience.
Faas BHW, Westra D, de Munnik SA, van Rij M, Marcelis C, Joosten S, Krapels I, Vernimmen V, Heijligers M, Willemsen MH, de Leeuw N, Rinne T, Pfundt R, Smeekens SP, Stegmann SPA, Macville M, Sikkel E, Coumans A, Wijnberger L, Derks I, van Lent-Albrechts J, Hofste T, Timmermans R, van den End J, Stevens SJC, Feenstra I.
Faas BHW, et al. Among authors: van lent albrechts j.
Prenat Diagn. 2023 Apr;43(4):527-543. doi: 10.1002/pd.6314. Epub 2023 Feb 5.
Prenat Diagn. 2023.
PMID: 36647814
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Viral load, gene expression and mapping of viral integration sites in HPV16-associated HNSCC cell lines.
Olthof NC, Huebbers CU, Kolligs J, Henfling M, Ramaekers FC, Cornet I, van Lent-Albrechts JA, Stegmann AP, Silling S, Wieland U, Carey TE, Walline HM, Gollin SM, Hoffmann TK, de Winter J, Kremer B, Klussmann JP, Speel EJ.
Olthof NC, et al. Among authors: van lent albrechts ja.
Int J Cancer. 2015 Mar 1;136(5):E207-18. doi: 10.1002/ijc.29112. Epub 2014 Aug 14.
Int J Cancer. 2015.
PMID: 25082736
Free PMC article.
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Clinically manifest X-linked recessive ichthyosis in a female due to a homozygous interstitial 1·6-Mb deletion of Xp22.31.
Nagtzaam IF, Stegmann AP, Steijlen PM, Herbergs J, Van Lent-Albrechts JA, Van Geel M, Van Steensel MA.
Nagtzaam IF, et al. Among authors: van lent albrechts ja.
Br J Dermatol. 2012 Apr;166(4):905-7. doi: 10.1111/j.1365-2133.2011.10685.x. Epub 2012 Feb 6.
Br J Dermatol. 2012.
PMID: 21985695
No abstract available.
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