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	1.	Lack of knowledge and training affects quality of hospice care for persons with dementia. [electronic resource] by Kirchhoff, Maria Producer: 20021226 In: The American journal of hospice & palliative care vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Polydactyly in a boy with Smith-Magenis syndrome. [electronic resource] by MarianneJensen, Lisbeth Kirchhoff, Maria Producer: 20051221 In: Clinical dysmorphology vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	3.	Automatic analysis of multiplex ligation-dependent probe amplification products (exemplified by a commercial kit for prenatal aneuploidy detection). [electronic resource] by Gerdes, Tommy Kirchhoff, Maria Bryndorf, Thue Producer: 20060120 In: Electrophoresis vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Investigation of patients with mental retardation and dysmorphic features using comparative genomic hybridization and subtelomeric multiplex ligation dependent probe amplification. [electronic resource] by Kirchhoff, Maria Gerdes, Tommy Brunebjerg, Stine Bryndorf, Thue Producer: 20060810 In: American journal of medical genetics. Part A vol. 139 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Familial craniosynostosis associated with a microdeletion involving the NFIA gene. [electronic resource] by Nyboe, Daniel Kreiborg, Sven Kirchhoff, Maria Hove, Hanne B Producer: 20160419 In: Clinical dysmorphology vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	MLPA analysis for a panel of syndromes with mental retardation reveals imbalances in 5.8% of patients with mental retardation and dysmorphic features, including duplications of the Sotos syndrome and Williams-Beuren syndrome regions. [electronic resource] by Kirchhoff, Maria Bisgaard, Anne-Marie Bryndorf, Thue Gerdes, Tommy Producer: 20070322 In: European journal of medical genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	A 15q24 microduplication, reciprocal to the recently described 15q24 microdeletion, in a boy sharing clinical features with 15q24 microdeletion syndrome patients. [electronic resource] by Kiholm Lund, Ann-Britt Hove, Hanne Dahlgaard Kirchhoff, Maria Producer: 20090310 In: European journal of medical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Neonatal hyperinsulinemic hypoglycemia in a patient with 9p deletion syndrome. [electronic resource] by Bayat, Allan Kirchhoff, Maria Madsen, Camilla Gøbel Kreiborg, Sven Producer: 20190321 In: European journal of medical genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Mapping genomic deletions down to the base: a quantitative copy number scanning approach used to characterise and clone the breakpoints of a recurrent 7p14.2p15.3 deletion. [electronic resource] by Dunø, Morten Hove, Hanne Kirchhoff, Maria Devriendt, Koenraad Schwartz, Marianne Producer: 20050223 In: Human genetics vol. 115 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Twins with mental retardation and an interstitial deletion 7q34q36.2 leading to the diagnosis of long QT syndrome. [electronic resource] by Bisgaard, Anne-Marie Rackauskaite, Gija Thelle, Thomas Kirchhoff, Maria Bryndorf, Thue Producer: 20060530 In: American journal of medical genetics. Part A vol. 140 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Familial craniofacial abnormality and polymicrogyria associated with a microdeletion affecting the NFIA gene. [electronic resource] by Bayat, Allan Kirchhoff, Maria Madsen, Camilla G Roos, Laura Kreiborg, Sven Producer: 20180827 In: Clinical dysmorphology vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Monozygotic twins with a de novo 0.32 Mb 16q24.3 deletion, including TUBB3 presenting with developmental delay and mild facial dysmorphism but without overt brain malformation. [electronic resource] by Grønborg, Sabine Kjaergaard, Susanne Hove, Hanne Larsen, Vibeke André Kirchhoff, Maria Producer: 20160829 In: American journal of medical genetics. Part A vol. 167A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Facial asymmetry associated with small and large intestinal atresia, and ipsilateral malformations of eye, skin, and extremities. [electronic resource] by Hove, Hanne Dahlgaard Bisgaard, Anne-Marie Nissen, Kamilla Rothe Kirchhoff, Maria Producer: 20080527 In: Clinical dysmorphology vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	A 17q21.31 microduplication, reciprocal to the newly described 17q21.31 microdeletion, in a girl with severe psychomotor developmental delay and dysmorphic craniofacial features. [electronic resource] by Kirchhoff, Maria Bisgaard, Anne-Marie Duno, Morten Hansen, Flemming Juul Schwartz, Marianne Producer: 20070920 In: European journal of medical genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Multiplex ligation-dependent probe amplification (MLPA) in prenatal diagnosis-experience of a large series of rapid testing for aneuploidy of chromosomes 13, 18, 21, X, and Y. [electronic resource] by Gerdes, Tommy Kirchhoff, Maria Lind, Anne-Marie Vestergaard Larsen, Gitte Kjaergaard, Susanne Producer: 20090220 In: Prenatal diagnosis vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Interstitial deletion of the short arm of chromosome 1 (1p13.1p21.1) in a girl with mental retardation, short stature and colobomata. [electronic resource] by Bisgaard, Anne-Marie Rasmussen, Leif Normann Møller, Hans Ulrik Kirchhoff, Maria Bryndorf, Thue Producer: 20070518 In: Clinical dysmorphology vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Fetal ventriculomegaly due to familial submicroscopic terminal 6q deletions. [electronic resource] by Wadt, Karin Jensen, Lisa Neerup Bjerglund, Lise Lundstrøm, Majken Kirchhoff, Maria Kjaergaard, Susanne Producer: 20130430 In: Prenatal diagnosis vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Computer-assisted prenatal aneuploidy screening for chromosome 13, 18, 21, X and Y based on multiplex ligation-dependent probe amplification (MLPA). [electronic resource] by Gerdes, Tommy Kirchhoff, Maria Lind, Anne-Marie Larsen, Gitte Vestergaard Schwartz, Marianne Lundsteen, Claes Producer: 20050705 In: European journal of human genetics : EJHG vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	CD4+ CD31+ recent thymic emigrants in CHD7 haploinsufficiency (CHARGE syndrome): a case. [electronic resource] by Assing, Kristian Nielsen, Christian Kirchhoff, Maria Madsen, Hans O Ryder, Lars P Fisker, Niels Producer: 20140324 In: Human immunology vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	[Chromosome aberrations in mentally retarded and dysmorphic patients with normal karyotypes]. [electronic resource] by Kirchhoff, Maria Pedersen, Søren Kjeldsen, Eigil Rose, Hanne Dunø, Morten Kølvraa, Steen Lundsteen, Claes Producer: 20050104 In: Ugeskrift for laeger vol. 166 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 45 results.