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Results:
1-16
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Results: 16
Authors:
MEDICA I
LOGAR N
PETERLIN B
Citation: I. Medica et al., CONGENITAL AND EARLY-ONSET MYOTONIC-DYSTROPHY - CORRELATION OF CLINICAL AND MOLECULAR ANALYSIS, European journal of human genetics, 6, 1998, pp. 1130-1130
Authors:
MEDICA I
LOGAR N
BABAROVIAE JM
PETERLIN B
Citation: I. Medica et al., CARDIAC INVOLVEMENT IN MYOTONIC-DYSTROPHY, European journal of human genetics, 6, 1998, pp. 1131-1131
Authors:
LOGAR N
VELIKONJA N
FLISAR D
KOBAL J
JERMAN J
PETERLIN B
Citation: N. Logar et al., INDICATION FOR MEIOTIC DRIVE IN HUNTINGTONS-DISEASE, European journal of human genetics, 6, 1998, pp. 3029-3029
Authors:
VELIKONJA N
LOGAR N
ZIDAR J
MEDICA I
JERMAN J
PETERLIN B
Citation: N. Velikonja et al., SEGREGATION DISTORTION OF MYOTONIC-DYSTROPHY ALLELES IN SLOVENE POPULATION, European journal of human genetics, 6, 1998, pp. 3036-3036
Authors:
PETROVIE D
ZORC M
KEBER I
PETERLIN B
Citation: D. Petrovie et al., ANGIOTENSIN-I-CONVERTING-ENZYME GENE POLYMORPHISM AND ANGIOTENSINOGENGENE POLYMORPHISM - POSSIBLE RISK-FACTORS FOR PREMATURE CORONARY-ARTERY DISEASE IN SLOVENIA, European journal of human genetics, 6, 1998, pp. 3069-3069
Authors:
DEVILEE P
HERMANS J
EYFJORD J
BORRESEN AL
LIDEREAU R
SOBOL H
BORG A
CLETONJANSEN AM
OLAH E
COHEN B
SCHERNECK S
HAMANN U
PETERLIN B
CALIGO M
BIGNON YL
MAUGARD C
ANDERSEN TI
ODEGAND AEM
BIECHE I
BIRNBAUM D
CORNELISSE CJ
SZTAN M
STEEL MR
SEITZ S
LOGAR N
GOLOUH R
GHIMENTI C
BRUELLE S
JOALLAND MP
Citation: P. Devilee et al., LOSS OF HETEROZYGOSITY AT 7Q31 IN BREAST-CANCER - RESULTS FROM AN INTERNATIONAL COLLABORATIVE STUDY-GROUP, Genes, chromosomes & cancer, 18(3), 1997, pp. 193-199
Authors:
PETERLIN B
Citation: B. Peterlin, GENETIC SERVICES IN SLOVENIA, European journal of human genetics, 5, 1997, pp. 159-162
Authors:
PETERLIN B
KUNEJ T
ZOM B
DROBNIC S
GREGORIC J
DEBEVEC M
Citation: B. Peterlin et al., STERILITY ASSOCIATED WITH Y-CHROMOSOME ABNORMALITIES, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 120-120
Authors:
TURCO AE
BRESIN E
ROSSETTI S
PETERLIN B
MORANDI R
PIGNATTI PF
Citation: Ae. Turco et al., RAPID DNA-BASED PRENATAL-DIAGNOSIS BY GENETIC-LINKAGE IN 3 FAMILIES WITH ALPORTS-SYNDROME, American journal of kidney diseases, 30(2), 1997, pp. 174-179
Authors:
PETERLIN B
ZIDAR J
MEZNARICPETRUSA M
ZUPANCIC N
Citation: B. Peterlin et al., GENETIC EPIDEMIOLOGY OF DUCHENNE AND BECKER MUSCULAR-DYSTROPHY IN SLOVENIA, Clinical genetics, 51(2), 1997, pp. 94-97
Authors:
MEDICA I
MARKOVIC D
PETERLIN B
Citation: I. Medica et al., GENETIC EPIDEMIOLOGY OF MYOTONIC-DYSTROPHY IN ISTRIA, CROATIA, Acta neurologica Scandinavica, 95(3), 1997, pp. 164-166
Authors:
RUDOLPH G
NASEMANN JE
BENGISU M
KAMPIK A
ZERRES K
PETERLIN B
MEITINGER T
Citation: G. Rudolph et al., PAX2 GENE MUTATION ANALYSIS IN A FAMILY WITH OPTIC-NERVE COLOBOMA ANDAUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE (ADPKD) - EXCLUSION OF LINKAGE OF AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE TO LOCI ON CHROMOSOME-4 AND CHROMOSOME-16, Vision research, 36, 1996, pp. 445-445
Authors:
SMAHI A
HYDENGRANSKOG C
PETERLIN B
VABRES P
HEUERTZ S
FULCHIGNONILATAUD MC
DAHL N
LABRUNE P
LEMAREC B
PIUSSAN C
TAIEB A
VONKOSKULL H
HORSCAYLA MC
Citation: A. Smahi et al., THE GENE FOR THE FAMILIAL FORM OF INCONTINENTIA PIGMENTI (IP2) MAPS TO THE DISTAL PART OF XQ28, Human molecular genetics, 3(2), 1994, pp. 273-278
Authors:
PETERLIN B
Citation: B. Peterlin, GENETIC-COUNSELING IN INCONTINENTIA PIGMENTI, European journal of obstetrics, gynecology, and reproductive biology, 55(1), 1994, pp. 53-53
Authors:
PETERLIN B
PODRUMAC B
STIRN E
PERKOVIC T
Citation: B. Peterlin et al., A CLINICAL AND GENETIC-STUDY OF INCONTINENTIA PIGMENTI, Journal of Medical Genetics, 31(2), 1994, pp. 175-175
Authors:
SMAHI A
PETERLIN B
ONODERA O
TSUJI S
FULCHIGNONILATAUD MC
Citation: A. Smahi et al., USE OF A RADIATION-REDUCED HYBRID PANEL FOR THE LOCALIZATION OF 7 MARKERS IN THE XQ28 REGION OF THE HUMAN GENOME, Annales de genetique, 37(1), 1994, pp. 11-13
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