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9 results found

no	title	author	magazine	year	volume	issue	page(s)	type
1	A gene responsible for cavernous malformations of the brain maps to chromosome 7q	Dubovsky, Jan		1995	4	3	p. 453-458	article
2	A G-to-T transversion at the +5 position of intron 1 in the glutaryl CoA dehydrogenase gene is associated with the island Lake variant of glutaric acidemia type I	Greenberg, Cheryl R.		1995	4	3	p. 493-495	article
3	A novel point mutation in the Cu/Zn superoxide dismutase gene in a patient with familial amyotrophic lateral sclerosis	Ikeda, M.		1995	4	3	p. 491-492	article
4	Expression of the neurofibromatosis 2 (NF2) gene isoforms during rat embryonic development	Gutmann, David H.		1995	4	3	p. 471-478	article
5	Genetic heterogeneity of autosomal recessive limbgirdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locus	Allamand, V.		1995	4	3	p. 459-463	article
6	Linkage of posterior polymorphous corneal dystrophy to 20q11	Héon, Elise		1995	4	3	p. 485-488	article
7	Recombination rates across the HLA complex: use of microsatellites as a rapid screen for recombinant chromosomes	Martin, Maureen		1995	4	3	p. 423-428	article
8	Sets of short tandem repeat polymorphisms for efficient linkage screening of the human genome	Dubovsky, Jan		1995	4	3	p. 449-452	article
9	Tissue-specific expression of a FMR1/β-galactosidase fusion gene in transgenic mice	Hergersberg, Martin		1995	4	3	p. 359-366	article

9 results found

Koninklijke Bibliotheek - National Library of the Netherlands