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	1.	Obesity, rather than menstrual cycle pattern or follicle cohort size, determines hyperinsulinaemia, dyslipidaemia and hypertension in ageing women with polycystic ovary syndrome. [electronic resource] by Elting, M W Korsen, T J Schoemaker, J Producer: 20020422 In: Clinical endocrinology vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Prevalence of diabetes mellitus, hypertension and cardiac complaints in a follow-up study of a Dutch PCOS population. [electronic resource] by Elting, M W Korsen, T J Bezemer, P D Schoemaker, J Producer: 20010503 In: Human reproduction (Oxford, England) vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Women with polycystic ovary syndrome gain regular menstrual cycles when ageing. [electronic resource] by Elting, M W Korsen, T J Rekers-Mombarg, L T Schoemaker, J Producer: 20000210 In: Human reproduction (Oxford, England) vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	The rise of estradiol and inhibin B after acute stimulation with follicle-stimulating hormone predict the follicle cohort size in women with polycystic ovary syndrome, regularly menstruating women with polycystic ovaries, and regularly menstruating women with normal ovaries. [electronic resource] by Elting, M W Kwee, J Schats, R Rekers-Mombarg, L T Schoemaker, J Producer: 20010503 In: The Journal of clinical endocrinology and metabolism vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Comparison of endocrine tests with respect to their predictive value on the outcome of ovarian hyperstimulation in IVF treatment: results of a prospective randomized study. [electronic resource] by Kwee, J Elting, M W Schats, R Bezemer, P D Lambalk, C B Schoemaker, J Producer: 20040308 In: Human reproduction (Oxford, England) vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Informed consent for exome sequencing in diagnostics: exploring first experiences and views of professionals and patients. [electronic resource] by Rigter, T van Aart, C J A Elting, M W Waisfisz, Q Cornel, M C Henneman, L Producer: 20141121 In: Clinical genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Fatal neonatal hypertrophic cardiomyopathy caused by compound heterozygous truncating MYBPC3 mutation. [electronic resource] by Alsters, S Wong, L Peferoen, L Niessen, H W M Bikker, H Elting, M W Houweling, A C Publication details: Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation May 2019 In: Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	[Maternal uniparental disomy 14; differential diagnosis with Prader-Willi syndrome]. [electronic resource] by Tamminga, Saskia Stalman, Susanne E Kamp, Gerdine A Hendriks, Yvonne M C Knegt, A C Lia Elting, M W Mariet Producer: 20151222 In: Nederlands tijdschrift voor geneeskunde vol. 159 Availability: No items available. Save to lists Add to cart (remove)
	9.	Abnormal eyeblink conditioning is an early marker of cerebellar dysfunction in preclinical SCA3 mutation carriers. [electronic resource] by van Gaalen, J Maas, R P P W M Ippel, E F Elting, M W van Spaendonck-Zwarts, K Y Vermeer, S Verschuuren-Bemelmans, C Timmann, D van de Warrenburg, Bart P Producer: 20190603 In: Experimental brain research vol. 237 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Further audiovestibular characterization of DFNB77, caused by deleterious variants in LOXHD1, and investigation into the involvement of Fuchs corneal dystrophy. [electronic resource] by Wesdorp, M Schreur, V Beynon, A J Oostrik, J van de Kamp, J M Elting, M W van den Boogaard, M-J H Feenstra, I Admiraal, R J C Kunst, H P M Hoyng, C B Kremer, H Yntema, H G Pennings, R J E Schraders, M Producer: 20191115 In: Clinical genetics vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Prenatal testing for Huntington's disease in the Netherlands from 1998 to 2008. [electronic resource] by van Rij, M C de Koning Gans, P A M Aalfs, C M Elting, M Ippel, P F Maat-Kievit, J A Vermeer, S Verschuuren-Bemelmans, C C van Belzen, M J Belfroid, R D M Losekoot, M Geraedts, J P M Roos, R A C Tibben, A de Die-Smulders, C E M Bijlsma, E K Producer: 20140718 In: Clinical genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)