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Ophthalmic Genetics|November 12, 1998
Intrafamilial variability of the ocular phenotype in a Polish family with a missense mutation (A63D) in the Norrie disease geneJ Zaremba, S Feil, J Juszko, et al.European Journal of Human Genetics : EJHG|January 1, 1997
Erythrocyte glucose-6-phosphate dehydrogenase deficiency in Poland--a study on the 563 and 1311 mutations of the G6PD geneE Jabłońska-Skwiecińska, J G Zimowski, J Kłopocka, et al.Neurologia I Neurochirurgia Polska|May 3, 2000
[Detecting carriers of a deletion in the dystrophin gene in families with a single case of Duchenne/Becker muscular dystrophy]M Bisko, J G Zimowski, D Hoffman-Zacharska, et al.Neurologia I Neurochirurgia Polska|March 1, 1996
[Detection of dystrophin gene mutation carrier state]M Bisko, J G Zimowski, E Fidziańska, et al.Pneumonologia I Alergologia Polska|June 4, 1999
[Use of pleuro-peritoneal shunt in the treatment of chronic chylothorax]P Wójcik, T J Otto, R Jagiełło, et al.Human Genetics|January 1, 1984
Prenatal diagnosis of Sanfilippo disease type BW J Kleijer, J G Huijmans, W Blom, et al.Acta Neurobiologiae Experimentalis|January 1, 1993
Interrelationship between gene, its product and phenotype in Duchenne and Becker muscular dystrophyI Hausmanowa-Petrusewicz, J Zaremba, A Fidziańska, et al.Journal of Applied Genetics|May 11, 2010
Subtelomeric rearrangements in Polish subjects with intellectual disability and dysmorphic featuresJ Bogdanowicz, B Pawłowska, A Ilnicka, et al.Neurologia I Neurochirurgia Polska|January 1, 1996
[The alpha-fetoprotein level analysis in open neural tube defects and chromosomal aberrations in the fetus]A Ilnicka, B Pawłowska, J Czyzewska, et al.Folia Neuropathologica|January 1, 1996
Adult schizophrenic-like variant of adrenoleukodystrophyG M Szpak, E Lewandowska, B Schmidt-Sidor, et al.Pageof 6