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Results: 3
IN-VITRO SPLICING DEFICIENCY INDUCED BY A C-TO-T MUTATION AT POSITION--3 IN THE INTRON-10 ACCEPTOR SITE OF THE PHENYLALANINE-HYDROXYLASE GENE IN A PATIENT WITH PHENYLKETONURIA
Authors: JARUZELSKA J ABADIE V DAUBENTONCARAFA Y BRODY E MUNNICH A MARIE J
Citation: J. Jaruzelska et al., IN-VITRO SPLICING DEFICIENCY INDUCED BY A C-TO-T MUTATION AT POSITION--3 IN THE INTRON-10 ACCEPTOR SITE OF THE PHENYLALANINE-HYDROXYLASE GENE IN A PATIENT WITH PHENYLKETONURIA, The Journal of biological chemistry, 270(35), 1995, pp. 20370-20375
IN-SITU LOCALIZATION OF HLA CLASS-I MESSENGER-RNA IN HUMAN TESTIS
Authors: JANITZ M FISZER D JARUZELSKA J SIMON AK BIRO A SACHS JA KURPISZ M
Citation: M. Janitz et al., IN-SITU LOCALIZATION OF HLA CLASS-I MESSENGER-RNA IN HUMAN TESTIS, Experimental and clinical immunogenetics, 10(4), 1993, pp. 202-207
A SIMPLIFIED METHOD FOR DETECTION OF THE MUTATIONS PREDOMINANTLY CAUSING CYSTIC-FIBROSIS AND PHENYLKETONURIA IN POLISH FAMILIES
Authors: WITT M JARUZELSKA J KUCZORA I MATUSZAK R CICHY W BORSKI K
Citation: M. Witt et al., A SIMPLIFIED METHOD FOR DETECTION OF THE MUTATIONS PREDOMINANTLY CAUSING CYSTIC-FIBROSIS AND PHENYLKETONURIA IN POLISH FAMILIES, Clinical genetics, 44(1), 1993, pp. 44-45
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