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	1.	European multicentre studies in the field of obstetrics. [electronic resource] by van Geijn, H P Lachmeijer, A M Copray, F J Producer: 19931004 In: European journal of obstetrics, gynecology, and reproductive biology vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Concordance for pre-eclampsia in monozygous twins. [electronic resource] by Lachmeijer, A M Aarnoudse, J G ten Kate, L P Pals, G Dekker, G A Producer: 19990121 In: British journal of obstetrics and gynaecology vol. 105 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Two novel WTX mutations underscore the unpredictability of male survival in osteopathia striata with cranial sclerosis. [electronic resource] by Perdu, B Lakeman, P Mortier, G Koenig, R Lachmeijer, A M A Van Hul, W Producer: 20130822 In: Clinical genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Polymorphisms in the tumor necrosis factor and lymphotoxin-alpha gene region and preeclampsia. [electronic resource] by Lachmeijer, A M Crusius, J B Pals, G Dekker, G A Arngrímsson, R ten Kate, L P Producer: 20011018 In: Obstetrics and gynecology vol. 98 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Change in paternity: a risk factor for preeclampsia in multiparous women? [electronic resource] by Tubbergen, P Lachmeijer, A M Althuisius, S M Vlak, M E van Geijn, H P Dekker, G A Producer: 20000309 In: Journal of reproductive immunology vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Prenatal detection of Noonan syndrome by mutation analysis of the PTPN11 and the KRAS genes. [electronic resource] by Houweling, A C de Mooij, Y M van der Burgt, I Yntema, H G Lachmeijer, A M A Go, A T J I Producer: 20100608 In: Prenatal diagnosis vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Mutations in the gene for methylenetetrahydrofolate reductase, homocysteine levels, and vitamin status in women with a history of preeclampsia. [electronic resource] by Lachmeijer, A M Arngrímsson, R Bastiaans, E J Pals, G ten Kate, L P de Vries, J I Kostense, P J Aarnoudse, J G Dekker, G A Producer: 20010329 In: American journal of obstetrics and gynecology vol. 184 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	A genome-wide scan reveals a maternal susceptibility locus for pre-eclampsia on chromosome 2p13. [electronic resource] by Arngrímsson, R Sigurõardóttir, S Frigge, M L Bjarnadóttir, R I Jónsson, T Stefánsson, H Baldursdóttir, A Einarsdóttir, A S Palsson, B Snorradóttir, S Lachmeijer, A M Nicolae, D Kong, A Bragason, B T Gulcher, J R Geirsson, R T Stefánsson, K Producer: 20000127 In: Human molecular genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	A genome-wide scan for preeclampsia in the Netherlands. [electronic resource] by Lachmeijer, A M Arngrímsson, R Bastiaans, E J Frigge, M L Pals, G Sigurdardóttir, S Stéfansson, H Pálsson, B Nicolae, D Kong, A Aarnoudse, J G Gulcher, J R Dekker, G A ten Kate, L P Stéfansson, K Producer: 20020208 In: European journal of human genetics : EJHG vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Refining the phenotype of alpha-1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly. [electronic resource] by Morris-Rosendahl, D J Najm, J Lachmeijer, A M A Sztriha, L Martins, M Kuechler, A Haug, V Zeschnigk, C Martin, P Santos, M Vasconcelos, C Omran, H Kraus, U Van der Knaap, M S Schuierer, G Kutsche, K Uyanik, G Producer: 20081215 In: Clinical genetics vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Germline Mutations in RASA1 Are Not Found in Patients with Klippel-Trenaunay Syndrome or Capillary Malformation with Limb Overgrowth. [electronic resource] by Revencu, N Boon, L M Dompmartin, A Rieu, P Busch, W L Dubois, J Forzano, F van Hagen, J M Halbach, S Kuechler, A Lachmeijer, A M A Lähde, J Russell, L Simola, K O J Mulliken, J B Vikkula, M Producer: 20130627 In: Molecular syndromology vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)