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Results: 1-11 |
Results: 11
A TRANSCRIPTIONAL MAP OF THE FMF REGION
Authors: BERNOT A HEILIG R CLEPET C SMAOUI N DASILVA C PETIT JL DEVAUD C CHIANNILKULCHAI N FIZAMES C SAMSON D CRUAUD C CALOUSTIAN C GYAPAY G DELPECH M WEISSENBACH J
Citation: A. Bernot et al., A TRANSCRIPTIONAL MAP OF THE FMF REGION, Genomics, 50(2), 1998, pp. 147-160
EVIDENCE OF CHROMOSOMAL INVERSION USING FLUORESCENCE IN-SITU HYBRIDIZATION TO STRETCHED DNA
Authors: SALOMONNGUYEN F LECONIATBUSSON M HEILIG R CAMPION D WEISSENBACH J BERGER R
Citation: F. Salomonnguyen et al., EVIDENCE OF CHROMOSOMAL INVERSION USING FLUORESCENCE IN-SITU HYBRIDIZATION TO STRETCHED DNA, Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie, 321(6), 1998, pp. 447-452
A CANDIDATE GENE FOR FAMILIAL MEDITERRANEAN FEVER
Authors: BERNOT A CLEPET C DASILVA C DEVAUD C PETIT JL CALOUSTIAN C CRUAUD C SAMSON D PULCINI F WEISSENBACH J HEILIG R NOTANICOLA C DOMINGO C ROZENBAUM M BENCHETRIT E TOPALOGLU R DEWALLE M DROSS C HADJARI P DUPONT M DEMAILLE J TOUITOU I SMAOUI N NEDELEC B MERY JP CHAABOUNI H DELPECH M GRATEAU G
Citation: A. Bernot et al., A CANDIDATE GENE FOR FAMILIAL MEDITERRANEAN FEVER, Nature genetics, 17(1), 1997, pp. 25-31
A HUMAN HOMOLOG OF THE DROSOPHILA EYES ABSENT GENE UNDERLIES BRANCHIOOTORENAL (BOR) SYNDROME AND IDENTIFIES A NOVEL GENE FAMILY
Authors: ABDELHAK S KALATZIS V HEILIG R COMPAIN S SAMSON D VINCENT C WEIL D CRUAUD C SAHLY I LEIBOVICI M BITNERGLINDZICZ M FRANCIS M LACOMBE D VIGNERON J CHARACHON R BOVEN K BEDBEDER P VANREGEMORTER N WEISSENBACH J PETIT C
Citation: S. Abdelhak et al., A HUMAN HOMOLOG OF THE DROSOPHILA EYES ABSENT GENE UNDERLIES BRANCHIOOTORENAL (BOR) SYNDROME AND IDENTIFIES A NOVEL GENE FAMILY, Nature genetics, 15(2), 1997, pp. 157-164
CLUSTERING OF MUTATIONS RESPONSIBLE FOR BRANCHIOOTORENAL (BOR) SYNDROME IN THE EYES ABSENT HOMOLOGOUS REGION (EYAHR) OF EYA1
Authors: ABDELHAK S KALATZIS V HEILIG R COMPAIN S SAMSON D VINCENT C LEVIACOBAS F CRUAUD C LEMERRER M MATHIEU M KONIG R VIGNERON J WEISSENBACH J PETIT C WEIL D
Citation: S. Abdelhak et al., CLUSTERING OF MUTATIONS RESPONSIBLE FOR BRANCHIOOTORENAL (BOR) SYNDROME IN THE EYES ABSENT HOMOLOGOUS REGION (EYAHR) OF EYA1, Human molecular genetics, 6(13), 1997, pp. 2247-2255
A NOVEL GENE THAT ENCODES A PROTEIN WITH A PUTATIVE SRC HOMOLOGY-3 DOMAIN IS A CANDIDATE GENE FOR FAMILIAL JUVENILE NEPHRONOPHTHISIS
Authors: SAUNIER S CALADO J HEILIG R SILBERMANN F BENESSY F MORIN G KONRAD M BROYER M GUBLER MC WEISSENBACH J ANTIGNAC C
Citation: S. Saunier et al., A NOVEL GENE THAT ENCODES A PROTEIN WITH A PUTATIVE SRC HOMOLOGY-3 DOMAIN IS A CANDIDATE GENE FOR FAMILIAL JUVENILE NEPHRONOPHTHISIS, Human molecular genetics, 6(13), 1997, pp. 2317-2323
TACTILE OPTICAL SENSOR FOR USE IN MINIMAL LY INVASIVE SURGERY
Authors: FISCHER H HEILIG R TRAPP R BRHEL K
Citation: H. Fischer et al., TACTILE OPTICAL SENSOR FOR USE IN MINIMAL LY INVASIVE SURGERY, Langenbecks Archiv fur Chirurgie, 1996, pp. 1290-1290
APOLIPOPROTEIN-E GENOTYPE DOES NOT AFFECT AGE AT ONSET IN PATIENTS WITH CHROMOSOME-14 ENCODED ALZHEIMERS-DISEASE
Authors: BRICE A TARDIEU S DIDIERJEAN O LEGUERN E MICHON A PILLON B HAHN V DUBOIS B PENET C AGID Y CAMPION D MARTINEZ M BABRON MC CLERGETDARPOUX F BELLIS M CALANDA A HEILIG R WEISSENBACH J MALLET J FREBOURG T HANNEQUIN D PUEL M LEDOZE F PASQUIER F ZIMMERMANN MA THOMASANTERION C MOREAU O
Citation: A. Brice et al., APOLIPOPROTEIN-E GENOTYPE DOES NOT AFFECT AGE AT ONSET IN PATIENTS WITH CHROMOSOME-14 ENCODED ALZHEIMERS-DISEASE, Journal of Medical Genetics, 33(2), 1996, pp. 174-175
MUTATIONS OF THE PRESENILIN-I GENE IN FAMILIES WITH EARLY-ONSET ALZHEIMERS-DISEASE
Authors: CAMPION D FLAMAN JM BRICE A HANNEQUIN D DUBOIS B MARTIN C MOREAU V CHARBONNIER F DIDIERJEAN O TARDIEU S PENET C PUEL M PASQUIER F LEDOZE F BELLIS G CALENDA A HEILIG R MARTINEZ M MALLET J BELLIS M CLERGETDARPOUX F AGID Y FREBOURG T
Citation: D. Campion et al., MUTATIONS OF THE PRESENILIN-I GENE IN FAMILIES WITH EARLY-ONSET ALZHEIMERS-DISEASE, Human molecular genetics, 4(12), 1995, pp. 2373-2377
THE NACP SYNUCLEIN GENE - CHROMOSOMAL ASSIGNMENT AND SCREENING FOR ALTERATIONS IN ALZHEIMER-DISEASE/
Authors: CAMPION D MARTIN C HEILIG R CHARBONNIER F MOREAU V FLAMAN JM PETIT JL HANNEQUIN D BRICE A FREBOURG T
Citation: D. Campion et al., THE NACP SYNUCLEIN GENE - CHROMOSOMAL ASSIGNMENT AND SCREENING FOR ALTERATIONS IN ALZHEIMER-DISEASE/, Genomics, 26(2), 1995, pp. 254-257
TIME-OPTIMIZED ANALYSIS OF SLIT-SCAN CHROMOSOME PROFILES ON A GENERAL-PURPOSE PERSONAL-COMPUTER
Authors: HEILIG R HAUSMANN M RENS W ATEN JA CREMER C
Citation: R. Heilig et al., TIME-OPTIMIZED ANALYSIS OF SLIT-SCAN CHROMOSOME PROFILES ON A GENERAL-PURPOSE PERSONAL-COMPUTER, Computer applications in the biosciences, 9(4), 1993, pp. 381-385
Risultati: 1-11 |