Format
Sort by

Send to

Choose Destination

Search results

Items: 5

1.

Genetic obesity: next-generation sequencing results of 1230 patients with obesity.

Kleinendorst L, Massink MPG, Cooiman MI, Savas M, van der Baan-Slootweg OH, Roelants RJ, Janssen ICM, Meijers-Heijboer HJ, Knoers NVAM, Ploos van Amstel HK, van Rossum EFC, van den Akker ELT, van Haaften G, van der Zwaag B, van Haelst MM.

J Med Genet. 2018 Sep;55(9):578-586. doi: 10.1136/jmedgenet-2018-105315. Epub 2018 Jul 3.

PMID:
29970488
2.

Recontacting in light of new genetic diagnostic techniques for patients with intellectual disability: Feasibility and parental perspectives.

Beunders G, Dekker M, Haver O, Meijers-Heijboer HJ, Henneman L.

Eur J Med Genet. 2018 Apr;61(4):213-218. doi: 10.1016/j.ejmg.2017.11.017. Epub 2017 Nov 27.

PMID:
29191497
3.

Outcome of surveillance and prophylactic salpingo-oophorectomy in asymptomatic women at high risk for ovarian cancer.

Meeuwissen PA, Seynaeve C, Brekelmans CT, Meijers-Heijboer HJ, Klijn JG, Burger CW.

Gynecol Oncol. 2005 May;97(2):476-82.

PMID:
15863147
4.

Deletions at chromosome regions 7q11.23 and 7q36 in a patient with Williams syndrome.

Wouters CH, Meijers-Heijboer HJ, Eussen BJ, van der Heide AA, van Luijk RB, van Drunen E, Beverloo BB, Visscher F, Van Hemel JO.

Am J Med Genet. 2001 Aug 15;102(3):261-5.

PMID:
11484204
5.

DNA diagnosis of Prader-Willi and Angelman syndromes with the probe PW71 (D15S63).

van den Ouweland AM, van der Est MN, Wesby-van Swaay E, Tijmensen TS, Los FJ, Van Hemel JO, Hennekam RC, Meijers-Heijboer HJ, Niermeijer MF, Halley DJ.

Hum Genet. 1995 May;95(5):562-7.

PMID:
7759079

Supplemental Content

Loading ...
Support Center