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Results: 1-13 |
Results: 13
MUTATION ANALYSIS IN THE NEUROFIBROMATOSIS-2 GENE
Authors: HERGERSBERG M BOLTSHAUSER E SCHINZEL A SPIEGEL R LANDAU K KATO R
Citation: M. Hergersberg et al., MUTATION ANALYSIS IN THE NEUROFIBROMATOSIS-2 GENE, European journal of human genetics, 6, 1998, pp. 4193-4193
STRUCTURAL DECOMPOSITION OF GENETIC DIVERSITY IN SCHIZOPHRENIC, SCHIZOAFFECTTVE, AND BIPOLAR PATIENTS
Authors: STASSEN HH BRIDLER R CAMENISCH I SCHINZEL A HERGERSBERG M SCHARFETTER C
Citation: Hh. Stassen et al., STRUCTURAL DECOMPOSITION OF GENETIC DIVERSITY IN SCHIZOPHRENIC, SCHIZOAFFECTTVE, AND BIPOLAR PATIENTS, American journal of medical genetics, 81(6), 1998, pp. 465-465
FUNCTIONAL POLYMORPHIC TRIPLET REPEATS IN PSYCHIATRIC-DISORDERS - AN ASSOCIATION STUDY
Authors: KATO R CAMENISCH I SCHARFETTER C SCHINZEL A STASSEN H HERGERSBERG M
Citation: R. Kato et al., FUNCTIONAL POLYMORPHIC TRIPLET REPEATS IN PSYCHIATRIC-DISORDERS - AN ASSOCIATION STUDY, American journal of medical genetics, 81(6), 1998, pp. 543-543
NEW MUTATION, 3905INST, ACCOUNTS FOR 4.8-PERCENT OF 1173 CF CHROMOSOMES IN SWITZERLAND AND CAUSES A SEVERE PHENOTYPE
Authors: HERGERSBERG M BALAKRISHNAN J BETTECKEN T CHEVALIERPORST F BRAGGER C BURGER R EINSCHENK I LIECHTIGALLATI S MORRIS M SCHORDERET D THONNEY F MOSER H MALIK N
Citation: M. Hergersberg et al., NEW MUTATION, 3905INST, ACCOUNTS FOR 4.8-PERCENT OF 1173 CF CHROMOSOMES IN SWITZERLAND AND CAUSES A SEVERE PHENOTYPE, Human genetics, 100(2), 1997, pp. 220-223
WISKOTT-ALDRICH SYNDROME - NO STRICT GENOTYPE-PHENOTYPE CORRELATIONS BUT CLUSTERING OF MISSENSE MUTATIONS IN THE AMINO-TERMINAL PART OF THEWASP GENE-PRODUCT
Authors: SCHINDELHAUER D WEISS M HELLEBRAND H GOLLA A HERGERSBERG M SEGER R BELOHRADSKY BH MEINDL A
Citation: D. Schindelhauer et al., WISKOTT-ALDRICH SYNDROME - NO STRICT GENOTYPE-PHENOTYPE CORRELATIONS BUT CLUSTERING OF MISSENSE MUTATIONS IN THE AMINO-TERMINAL PART OF THEWASP GENE-PRODUCT, Human genetics, 98(1), 1996, pp. 68-76
MUTATION ANALYSIS IN PATIENTS WITH X-LINKED RETINITIS-PIGMENTOSA
Authors: ZRENNER E LORENZ B WITTWER B APFELSTEDT E WISSINGER B HERGERSBERG M RUDOLPH G HERRMANN K ACHATZ H MEINDL A MEITINGER T
Citation: E. Zrenner et al., MUTATION ANALYSIS IN PATIENTS WITH X-LINKED RETINITIS-PIGMENTOSA, Vision research, 36, 1996, pp. 3231-3231
UNIPARENTAL DISOMY-7 IN SILVER-RUSSELL-SYNDROME AND PRIMORDIAL GROWTH-RETARDATION
Authors: KOTZOT D SCHMITT S BERNASCONI F ROBINSON WP LURIE IW ILYINA H MEHES K HAMEL BCJ OTTEN BJ HERGERSBERG M WERDER E SCHOENLE E SCHINZEL A
Citation: D. Kotzot et al., UNIPARENTAL DISOMY-7 IN SILVER-RUSSELL-SYNDROME AND PRIMORDIAL GROWTH-RETARDATION, Human molecular genetics, 4(4), 1995, pp. 583-587
TISSUE-SPECIFIC EXPRESSION OF A FMR1 BETA-GALACTOSIDASE FUSION GENE IN TRANSGENIC MICE/
Authors: HERGERSBERG M MATSUO K GASSMANN M SCHAFFNER W LUSCHER B RULICKE T AGUZZI A
Citation: M. Hergersberg et al., TISSUE-SPECIFIC EXPRESSION OF A FMR1 BETA-GALACTOSIDASE FUSION GENE IN TRANSGENIC MICE/, Human molecular genetics, 4(3), 1995, pp. 359-366
GENETIC-LINKAGE OF WAGNER DISEASE AND EROSIVE VITREORETINOPATHY TO CHROMOSOME 5Q13-14
Authors: BROWN DM GRAEMIGER RA HERGERSBERG M SCHINZEL A MESSMER EP NIEMEYER G SCHNEEBERGER SA STREB LM TAYLOR CM KIMURA AE WEINGEIST TA SHEFFIELD C STONE EM
Citation: Dm. Brown et al., GENETIC-LINKAGE OF WAGNER DISEASE AND EROSIVE VITREORETINOPATHY TO CHROMOSOME 5Q13-14, Archives of ophthalmology, 113(5), 1995, pp. 671-675
GENOTYPE AND PHENOTYPE CORRELATIONS IN WISKOTT-ALDRICH SYNDROME - VARIABLE EXPRESSION OR MUTATION DEPENDENT PHENOTYPES
Authors: SCHINDELHAUER D WEISS M HELLEBRAND H HERGERSBERG M SEGER R BELOHRADSKY BH MEINDL A
Citation: D. Schindelhauer et al., GENOTYPE AND PHENOTYPE CORRELATIONS IN WISKOTT-ALDRICH SYNDROME - VARIABLE EXPRESSION OR MUTATION DEPENDENT PHENOTYPES, American journal of human genetics, 57(4), 1995, pp. 1451-1451
A NEW MUTATION, 3905INST, IS PROMINENT AMONG SWISS CF CHROMOSOMES
Authors: HERGERSBERG M BALAKRISHNAN J BETTECKEN T BOZON D BRAGGER C BURGER R EINSCHENK I MORRIS M SCHORDERET D THONNEY F MOSER FH MALIK N
Citation: M. Hergersberg et al., A NEW MUTATION, 3905INST, IS PROMINENT AMONG SWISS CF CHROMOSOMES, American journal of human genetics, 57(4), 1995, pp. 1918-1918
TOWARDS THE CLONING OF THE WAS-GENE LOCUS - LINKAGE AND PHYSICAL MAPPING
Authors: MEINDL A SCHINDELHAUER D HELLEBRAND H HERGERSBERG M ROSS M MONACO AP MEITINGER T
Citation: A. Meindl et al., TOWARDS THE CLONING OF THE WAS-GENE LOCUS - LINKAGE AND PHYSICAL MAPPING, Cytogenetics and cell genetics, 67(4), 1994, pp. 343-343
DIRECT GENETIC DIAGNOSIS OF HUNTINGTONS-D ISEASE
Authors: SPIEGEL R WEIGELLWEBER M HERGERSBERG M SCHMID W
Citation: R. Spiegel et al., DIRECT GENETIC DIAGNOSIS OF HUNTINGTONS-D ISEASE, Schweizerische medizinische Wochenschrift, 123(48), 1993, pp. 2271-2277
Risultati: 1-13 |