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Journal of Medical Genetics|October 1, 1991
A cystic fibrosis patient homozygous for the nonsense mutation R553XJ Bal, M Stuhrmann, M Schloesser, et al.Pneumonologia I Alergologia Polska|September 25, 1999
[Frequency of mutations and genotypes of the CFTR gene in cystic fibrosis adults in Poland]M Witt, A Pogorzelski, J Bal, et al.Genetic Testing|September 25, 1999
Mutations in exon 3 of the PAH gene causing mild hyperphenylalaninemiaC Zekanowski, M Nowacka, M Gizewska, et al.Genetic Testing|September 12, 2001
High frequency of GJB2 gene mutations in Polish patients with prelingual nonsyndromic deafnessW Wiszniewski, L Sobieszczanska-Radoszewska, E Nowakowska-Szyrwinska, et al.Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|March 1, 1992
[Martin-Bell syndrome. Improved possibilities for molecular genetic diagnosis]B Zoll, J Bal, J Pohnke, et al.Pediatria Polska|August 1, 1995
[A study evaluating the correlation between the phenotype and genotype among 65 cystic fibrosis patients]A Nowakowska, J Bal, E Obersztyn, et al.Klinika Oczna|July 6, 2000
[The attempt to identify mutations in TIGR gene in Polish patients with primary open angle glaucoma]J Szaflik, A M Ambroziak, J Bal, et al.Acta Anaesthesiologica Belgica|January 1, 1980
Circulatory changes during a hypotensive technique of anesthesiaJ Delaruelle, E R Raman, V J Vanhuyse, et al.Acta Geneticae Medicae Et Gemellologiae|January 1, 1996
Molecular and clinical studies of Polish patients with Prader-Willi syndromeA Szpecht-Potocka, E Obersztyn, M Karwacki, et al.Human Genetics|August 1, 1991
Discrimination between recurrent mutation and identity by descent: application to point mutations in exon 11 of the cystic fibrosis (CFTR) geneJ Reiss, D N Cooper, J Bal, et al.Pageof 5