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Prenatal diagnosis of tetrasomy 9p in a 19-week-old fetus with Dandy-Walker malformation: a case report.
Prenat Diagn. 2004 Oct;24(10):796-8. doi: 10.1002/pd.850.
Prenat Diagn. 2004.
PMID: 15503289
'Identical' twins with discordant karyotypes.
Nieuwint A, Van Zalen-Sprock R, Hummel P, Pals G, Van Vugt J, Van Der Harten H, Heins Y, Madan K.
Nieuwint A, et al.
Prenat Diagn. 1999 Jan;19(1):72-6. doi: 10.1002/(sici)1097-0223(199901)19:1<72::aid-pd465>3.0.co;2-v.
Prenat Diagn. 1999.
PMID: 10073913
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Hepatoblastoma in a patient with a partial trisomy 9p syndrome: a case report.
Schnater JM, Schouten-van Meeteren AY, Heins YM, Aronson DC.
Schnater JM, et al. Among authors: heins ym.
Cancer Genet Cytogenet. 2005 Jan 1;156(1):77-9. doi: 10.1016/j.cancergencyto.2004.04.011.
Cancer Genet Cytogenet. 2005.
PMID: 15588861
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Variable phenotypes associated with 10q23 microdeletions involving the PTEN and BMPR1A genes.
Menko FH, Kneepkens CM, de Leeuw N, Peeters EA, Van Maldergem L, Kamsteeg EJ, Davidson R, Rozendaal L, Lasham CA, Peeters-Scholte CM, Jansweijer MC, Hilhorst-Hofstee Y, Gille JJ, Heins YM, Nieuwint AW, Sistermans EA.
Menko FH, et al. Among authors: heins ym.
Clin Genet. 2008 Aug;74(2):145-54. doi: 10.1111/j.1399-0004.2008.01026.x. Epub 2008 May 28.
Clin Genet. 2008.
PMID: 18510548
Free article.
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Double-minute chromatin bodies in HL-60 leukemia cells sensitive and resistant to differentiation inducing agents.
Schwartsmann G, Madan K, Heins Y, Pinedo HM, Leyva A.
Schwartsmann G, et al.
Cell Biol Int Rep. 1987 Sep;11(9):651-5. doi: 10.1016/0309-1651(87)90099-3.
Cell Biol Int Rep. 1987.
PMID: 3479266
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Rapid detection of microdeletions using fluorescence in situ hybridisation (FISH) on buccal smears.
Nieuwint AW, Van Hagen JM, Heins YM, Madan K, Ten Kate LP.
Nieuwint AW, et al. Among authors: heins ym.
J Med Genet. 2000 Jun;37(6):E4. doi: 10.1136/jmg.37.6.e4.
J Med Genet. 2000.
PMID: 10851257
Free PMC article.
No abstract available.
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