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Results: 1-9 |
Results: 9
ANALYSIS OF UNSTABLE DNA-SEQUENCE IN FRM1 GENE IN POLISH FAMILIES WITH FRAGILE-X SYNDROME
Authors: MILEWSKI M ZYGULSKA M BAL J DEELEN WH OBERSZTYN E BOCIAN E HALLEY DJJ HORST J MAZURCZAK T
Citation: M. Milewski et al., ANALYSIS OF UNSTABLE DNA-SEQUENCE IN FRM1 GENE IN POLISH FAMILIES WITH FRAGILE-X SYNDROME, Acta Biochimica Polonica, 43(2), 1996, pp. 383-388
NORTHERN THAILAND - PREVALENCE OF HEMOGLOBIN CONSTANT SPRING AND DELETIONAL ALPHA-THALASSEMIAS
Authors: ZYGULSKA M EIGEL A HELBIG B SANGUANSERMSRI T FLATZ G
Citation: M. Zygulska et al., NORTHERN THAILAND - PREVALENCE OF HEMOGLOBIN CONSTANT SPRING AND DELETIONAL ALPHA-THALASSEMIAS, American journal of human genetics, 57(4), 1995, pp. 999-999
FRAGILE-X PREMUTATION FREQUENCY IN NORTHERN THAILAND
Authors: EIGEL A ZYGULSKA M DOLSCHEID T BOGDANOVA N DWORNICZAK B STEGER F SANGUANSERMSRI T FLATZ G HORST J
Citation: A. Eigel et al., FRAGILE-X PREMUTATION FREQUENCY IN NORTHERN THAILAND, American journal of human genetics, 57(4), 1995, pp. 1838-1838
PHENYLKETONURIA IN SOUTHERN POLAND - A NEW SPLICE MUTATION IN INTRON-9 AT THE PAH LOCUS
Authors: ZYGULSKA M EIGEL A PIETRZYK JJ HORST J
Citation: M. Zygulska et al., PHENYLKETONURIA IN SOUTHERN POLAND - A NEW SPLICE MUTATION IN INTRON-9 AT THE PAH LOCUS, Human mutation, 4(4), 1994, pp. 297-299
PHENYLALANINE-HYDROXYLASE GENE - A NOVEL SPLICE MUTATION IN INTRON-2 IN 2 GERMAN AND POLISH FAMILIES WITH SEVERE PHENYLKETONURIA
Authors: ZYGULSKA M EIGEL A PIETRZYK JJ HORST J
Citation: M. Zygulska et al., PHENYLALANINE-HYDROXYLASE GENE - A NOVEL SPLICE MUTATION IN INTRON-2 IN 2 GERMAN AND POLISH FAMILIES WITH SEVERE PHENYLKETONURIA, Human mutation, 2(3), 1993, pp. 238-239
A NOVEL MUTATION IN EXON-8 OF THE PHENYLALANINE-HYDROXYLASE GENE IN THE POLISH POPULATION
Authors: ZYGULSKA M EIGEL A PIETRZYK JJ MINY P HORST J
Citation: M. Zygulska et al., A NOVEL MUTATION IN EXON-8 OF THE PHENYLALANINE-HYDROXYLASE GENE IN THE POLISH POPULATION, Human mutation, 2(1), 1993, pp. 74-76
FFU COMPLEX - AN ANALYSIS OF 491 CASES
Authors: LENZ W ZYGULSKA M HORST J
Citation: W. Lenz et al., FFU COMPLEX - AN ANALYSIS OF 491 CASES, Human genetics, 91(4), 1993, pp. 347-356
TESTING FOR FRAGILE X-SYNDROME IN 120 FAMILIES WITH A HISTORY OF MENTAL-RETARDATION
Authors: WITTWER B ZYGULSKA M MINY P EIGEL A HORST J
Citation: B. Wittwer et al., TESTING FOR FRAGILE X-SYNDROME IN 120 FAMILIES WITH A HISTORY OF MENTAL-RETARDATION, American journal of human genetics, 53(3), 1993, pp. 1513-1513
ANALYSIS OF FMR-1-GENE MUTATIONS IN 16 POLISH FAMILIES WITH FRA-X SYNDROME
Authors: ZYGULSKA M MILEWSKI M WITTWER B EIGEL A BAL J MAZURCZAK T HORST J
Citation: M. Zygulska et al., ANALYSIS OF FMR-1-GENE MUTATIONS IN 16 POLISH FAMILIES WITH FRA-X SYNDROME, American journal of human genetics, 53(3), 1993, pp. 1769-1769
Risultati: 1-9 |