Hansson K - Search Results

1

A near false-negative finding of mosaic trisomy 21--a cautionary tale.

Beverstock GC, Hansson K, Helderman-van den Enden AT, Bröcker-Vriends A, Klumper F, Bartelings M, Dobbe-van Meerendonk W, Roosmalen JV, Kolkman PH, Kanhai HH. Beverstock GC, et al. Among authors: hansson k. Prenat Diagn. 1998 Jul;18(7):742-6. Prenat Diagn. 1998. PMID: 9706658

2

The outcome of pregnancies with confined placental chromosome mosaicism in cytotrophoblast cells.

Leschot NJ, Schuring-Blom GH, Van Prooijen-Knegt AC, Verjaal M, Hansson K, Wolf H, Kanhai HH, Van Vugt JM, Christiaens GC. Leschot NJ, et al. Among authors: hansson k. Prenat Diagn. 1996 Aug;16(8):705-12. doi: 10.1002/(SICI)1097-0223(199608)16:8<705::AID-PD930>3.0.CO;2-6. Prenat Diagn. 1996. PMID: 8878279

3

Low-level mosaicism for both trisomy 15 and monosomy-X in amniotic fluid cells confirmed in fetal tissues.

Hansson K, Poelma WM, Zondervan HA, Leschot NJ. Hansson K, et al. Prenat Diagn. 1998 Sep;18(9):975-8. Prenat Diagn. 1998. PMID: 9793985

4

The preserving of chorionic villi before establishing long-term cell cultures for cytogenetic analysis.

Hansson K, Schuring-Blom GH, Leschot NJ. Hansson K, et al. Prenat Diagn. 1995 Nov;15(11):1067-9. doi: 10.1002/pd.1970151112. Prenat Diagn. 1995. PMID: 8606886

5

Individuals with abnormal phenotype and normal G-banding karyotype: improvement and limitations in the diagnosis by the use of 24-colour FISH.

Bezrookove V, Hansson K, van der Burg M, van der Smagt JJ, Hilhorst-Hofstee Y, Wiegant J, Beverstock GC, Raap AK, Tanke H, Breuning MH, Rosenberg C. Bezrookove V, et al. Among authors: hansson k. Hum Genet. 2000 Apr;106(4):392-8. doi: 10.1007/s004390000268. Hum Genet. 2000. PMID: 10830905

6

Bannayan-Riley-Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive cases.

Hendriks YM, Verhallen JT, van der Smagt JJ, Kant SG, Hilhorst Y, Hoefsloot L, Hansson KB, van der Straaten PJ, Boutkan H, Breuning MH, Vasen HF, Bröcker-Vriends AH. Hendriks YM, et al. Among authors: hansson kb. Fam Cancer. 2003;2(2):79-85. doi: 10.1023/a:1025713815924. Fam Cancer. 2003. PMID: 14574156

7

Interstitial deletion of 6q without phenotypic effect.

Hansson K, Szuhai K, Knijnenburg J, van Haeringen A, de Pater J. Hansson K, et al. Am J Med Genet A. 2007 Jun 15;143A(12):1354-7. doi: 10.1002/ajmg.a.31783. Am J Med Genet A. 2007. PMID: 17506100

8

Molecular and clinical characterization of patients with a ring chromosome 11.

Hansson KB, Gijsbers AC, Oostdijk W, Rehbock JJ, de Snoo F, Ruivenkamp CA, Kant SG. Hansson KB, et al. Eur J Med Genet. 2012 Dec;55(12):708-14. doi: 10.1016/j.ejmg.2012.08.004. Epub 2012 Aug 23. Eur J Med Genet. 2012. PMID: 22975011

9

Ultrasound screening for fetal trisomies at 10-14 weeks' gestation.

Pajkrt E, Bilardo CM, van Lith JM, Mol BW, Hansson K, van Prooijen Knegt AC, Bleker OP. Pajkrt E, et al. Among authors: hansson k. Early Hum Dev. 1996 Dec 30;47 Suppl:S35-6. doi: 10.1016/s0378-3782(96)01816-6. Early Hum Dev. 1996. PMID: 9031837 No abstract available.

10

A complex chromosome 7q rearrangement identified in a patient with mental retardation, anxiety disorder, and autistic features.

Dauwerse JG, Ruivenkamp CA, Hansson K, Marijnissen GM, Peters DJ, Breuning MH, Hilhorst-Hofstee Y. Dauwerse JG, et al. Among authors: hansson k. Am J Med Genet A. 2010 Feb;152A(2):427-33. doi: 10.1002/ajmg.a.33203. Am J Med Genet A. 2010. PMID: 20082467

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

354 results

Search Page

Filters