Your search returned 6 results.

Results
	1.	Reproductive risks for paracentric inversion heterozygotes: Inversion or insertion? That is the question. [electronic resource] by Madan, K Nieuwint, A W M Producer: 20020626 In: American journal of medical genetics vol. 107 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Aberrant marker expression patterns on the CD34+CD38- stem cell compartment in acute myeloid leukemia allows to distinguish the malignant from the normal stem cell compartment both at diagnosis and in remission. [electronic resource] by van Rhenen, A Moshaver, B Kelder, A Feller, N Nieuwint, A W M Zweegman, S Ossenkoppele, G J Schuurhuis, G J Producer: 20070925 In: Leukemia vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Atypical progeroid syndrome: an unknown helicase gene defect? [electronic resource] by Ruijs, M W G van Andel, R N J Oshima, J Madan, K Nieuwint, A W M Aalfs, C M Producer: 20030430 In: American journal of medical genetics. Part A vol. 116A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Interstitial deletion in 3q in a patient with blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) and microcephaly, mild mental retardation and growth delay: clinical report and review of the literature. [electronic resource] by de Ru, M H Gille, J J P Nieuwint, A W M Bijlsma, J B van der Blij, J F van Hagen, J M Producer: 20050822 In: American journal of medical genetics. Part A vol. 137 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Familial Kleefstra syndrome due to maternal somatic mosaicism for interstitial 9q34.3 microdeletions. [electronic resource] by Willemsen, M H Beunders, G Callaghan, M de Leeuw, N Nillesen, W M Yntema, H G van Hagen, J M Nieuwint, A W M Morrison, N Keijzers-Vloet, S T M Hoischen, A Brunner, H G Tolmie, J Kleefstra, T Producer: 20110928 In: Clinical genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Variable phenotypes associated with 10q23 microdeletions involving the PTEN and BMPR1A genes. [electronic resource] by Menko, F H Kneepkens, C M F de Leeuw, N Peeters, E A J Van Maldergem, L Kamsteeg, E J Davidson, R Rozendaal, L Lasham, C A Peeters-Scholte, C M P Jansweijer, M C Hilhorst-Hofstee, Y Gille, J J P Heins, Y M Nieuwint, A W M Sistermans, E A Producer: 20081111 In: Clinical genetics vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)