AAAAAA

   
Results: 1-20 |
Results: 20
HIGH MUTATION DETECTION RATE IN THE COL4A5 COLLAGEN GENE IN SUSPECTEDALPORT-SYNDROME USING PCR AND DIRECT DNA-SEQUENCING
Authors: MARTIN P HEISKARI N ZHOU J LEINONEN A TUMELIUS T HERTZ JM BARKER D GREGORY M ATKIN C STYRKARSDOTTIR U NEUMANN H SPRINGATE J SHOWS T PETTERSSON E TRYGGVASON K
Citation: P. Martin et al., HIGH MUTATION DETECTION RATE IN THE COL4A5 COLLAGEN GENE IN SUSPECTEDALPORT-SYNDROME USING PCR AND DIRECT DNA-SEQUENCING, Journal of the American Society of Nephrology, 9(12), 1998, pp. 2291-2301
ORIGIN OF NONDISJUNCTION IN TRISOMY-8 AND TRISOMY-8 MOSAICISM
Authors: KARADIMA G BUGGE M NICOLAIDIS P VASSILOPOULOS D AVRAMOPOULOS D GRIGORIADOU M ALBRECHT B PASSARGE E ANNEREN G BLENNOW E CLAUSEN N GALLAVOUMVOURAKI A TSEZOU A KITSIOUTZELI S HAHNEMANN JM HERTZ JM HOUGE G KUKLIK M MACEK M LACOMBE D MILLER K MONCLA A PAJARES IL PATSALIS PC PRIEUR M VEKEMANS M VONBEUST G BRONDUMNIELSEN K PETERSEN MB
Citation: G. Karadima et al., ORIGIN OF NONDISJUNCTION IN TRISOMY-8 AND TRISOMY-8 MOSAICISM, European journal of human genetics, 6(5), 1998, pp. 432-438
NONDISJUNCTION OF CHROMOSOME-18
Authors: BUGGE M COLLINS A PETERSEN MB FISHER J BRANDT C HERTZ JM TRANEBJAERG L DELOZIERBLANCHET C NICOLAIDES P BRONDUMNIELSEN K MORTON N MIKKELSEN M
Citation: M. Bugge et al., NONDISJUNCTION OF CHROMOSOME-18, Human molecular genetics, 7(4), 1998, pp. 661-669
APOLIPOPROTEIN-E ALLELES IN MOTHERS OF TRISOMY-18 CONCEPTUSES
Authors: HANSEN C BUGGE M BRANDT CA HERTZ JM TRANEBJOAERG L MIKKELSEN M PETERSEN MB
Citation: C. Hansen et al., APOLIPOPROTEIN-E ALLELES IN MOTHERS OF TRISOMY-18 CONCEPTUSES, Clinical genetics, 53(4), 1998, pp. 321-322
A NOVEL MISSENSE MUTATION (402C-]T) IN EXON-1 IN THE EDA GENE IN A FAMILY WITH X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA
Authors: HERTZ JM HANSEN KN JUNCKER I KJELDSEN M GREGERSEN N
Citation: Jm. Hertz et al., A NOVEL MISSENSE MUTATION (402C-]T) IN EXON-1 IN THE EDA GENE IN A FAMILY WITH X-LINKED HYPOHIDROTIC ECTODERMAL DYSPLASIA, Clinical genetics, 53(3), 1998, pp. 205-209
MUTATION PATTERN IN BRUTON TYROSINE KINASE GENE IN 26 UNRELATED PATIENTS WITH X-LINKED AGAMMAGLOBULINEMIA
Authors: VORECHOVSKY I LUO LP HERTZ JM FROLAND SS KLEMOLA T FIORINI M QUINTI I PAGANELLI R OZSAHIN H HAMMARSTROM L WEBSTER ADB SMITH CIE
Citation: I. Vorechovsky et al., MUTATION PATTERN IN BRUTON TYROSINE KINASE GENE IN 26 UNRELATED PATIENTS WITH X-LINKED AGAMMAGLOBULINEMIA, Human mutation, 9(5), 1997, pp. 418-425
QUANTIFICATION, BY SOLID-PHASE MINISEQUENCING, OF THE TELOMERIC AND CENTROMERIC COPIES OF THE SURVIVAL MOTOR-NEURON GENE IN FAMILIES WITH SPINAL MUSCULAR-ATROPHY
Authors: SCHWARTZ M SORENSEN N HANSEN FJ HERTZ JM NORBY S TRANEBJAERG L SKOVBY F
Citation: M. Schwartz et al., QUANTIFICATION, BY SOLID-PHASE MINISEQUENCING, OF THE TELOMERIC AND CENTROMERIC COPIES OF THE SURVIVAL MOTOR-NEURON GENE IN FAMILIES WITH SPINAL MUSCULAR-ATROPHY, Human molecular genetics, 6(1), 1997, pp. 99-104
NONDISJUNCTION STUDIES IN TRISOMY-8
Authors: KARADIMA G AVRAMOPOULOS D GRIGORIADOU M PETERSEN MB ALBRECHT B ANNEREN G BLENNOW E BRONDUMNIELSEN K BUGGE M CLAUSEN N GALLAVOUMVOURAKI A HAHNEMANN JM HERTZ JM KITSIOUTZELI S LACOMBE D MILLER K MONCLA A PAJARES IL PASSARGE E PATSALIS PC PRIEUR M TSEZOU A VASSILOPOULOS D VEKEMANS M VONBEUST G
Citation: G. Karadima et al., NONDISJUNCTION STUDIES IN TRISOMY-8, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 105-105
APOLIPOPROTEIN-E ALLELES IN MOTHERS OF TRISOMY-18 CONCEPTUSES
Authors: BUGGE M HANSEN C BRANDT CA HERTZ JM TRANEBJAERG L MIKKELSEN M PETERSEN MB
Citation: M. Bugge et al., APOLIPOPROTEIN-E ALLELES IN MOTHERS OF TRISOMY-18 CONCEPTUSES, American journal of human genetics, 61(4), 1997, pp. 674-674
ORIGIN OF NONDISJUNCTION IN TRISOMY-8 AND TRISOMY-8 MOSAICISM
Authors: KARADIMA G BUGGE M NICOLAIDIS P VASSILOPOULOS D VONBEUST G PAJARES IL ALBRECHT B ANNEREN G AVRAMOPOULOS D BLENNOW E BRONDUMNIELSEN K CLAUSEN N GALLAVOUMVOURAKI A GRIGORIADOU M HAHNEMANN JM HERTZ JM KITSIOUTZELI S LACOMBE D MILLER K MONCLA A PASSARGE E PATSALIS PC PRIEUR M TSEZOU A VEKEMANS M PETERSEN MB
Citation: G. Karadima et al., ORIGIN OF NONDISJUNCTION IN TRISOMY-8 AND TRISOMY-8 MOSAICISM, American journal of human genetics, 61(4), 1997, pp. 732-732
EFFECTS OF ACUTE AND CHRONIC COCAINE ON MILK INTAKE, BODY-WEIGHT, ANDACTIVITY IN BOTTLE-FED AND CANNULA-FED RATS
Authors: WOLGIN DL HERTZ JM
Citation: Dl. Wolgin et Jm. Hertz, EFFECTS OF ACUTE AND CHRONIC COCAINE ON MILK INTAKE, BODY-WEIGHT, ANDACTIVITY IN BOTTLE-FED AND CANNULA-FED RATS, Behavioural pharmacology, 6(7), 1995, pp. 746-753
A NONSENSE MUTATION IN THE COL4A5 COLLAGEN GENE IN A FAMILY WITH X-LINKED JUVENILE ALPORT SYNDROME
Authors: HERTZ JM HEISKARI N ZHOU J JENSEN UB TRYGGVASON K
Citation: Jm. Hertz et al., A NONSENSE MUTATION IN THE COL4A5 COLLAGEN GENE IN A FAMILY WITH X-LINKED JUVENILE ALPORT SYNDROME, Kidney international, 47(1), 1995, pp. 327-332
EVOLUTION OF THE SINDBIS-VIRUS SUBGENOMIC MESSENGER-RNA PROMOTER IN CULTURED-CELLS
Authors: HERTZ JM HUANG HV
Citation: Jm. Hertz et Hv. Huang, EVOLUTION OF THE SINDBIS-VIRUS SUBGENOMIC MESSENGER-RNA PROMOTER IN CULTURED-CELLS, Journal of virology, 69(12), 1995, pp. 7768-7774
HOST-DEPENDENT EVOLUTION OF THE SINDBIS-VIRUS PROMOTER FOR SUBGENOMICMESSENGER-RNA SYNTHESIS
Authors: HERTZ JM HUANG HV
Citation: Jm. Hertz et Hv. Huang, HOST-DEPENDENT EVOLUTION OF THE SINDBIS-VIRUS PROMOTER FOR SUBGENOMICMESSENGER-RNA SYNTHESIS, Journal of virology, 69(12), 1995, pp. 7775-7781
A TAQI AND A BAMHI POLYMORPHISM IN THE COL4A4 GENE ON CHROMOSOME 2Q35-37
Authors: HERTZ JM MARIYAMA M THOMSEN A REEDERS ST KRUSE TA
Citation: Jm. Hertz et al., A TAQI AND A BAMHI POLYMORPHISM IN THE COL4A4 GENE ON CHROMOSOME 2Q35-37, Clinical genetics, 48(3), 1995, pp. 162-163
PARTIAL DELETION 11Q - REPORT OF A CASE WITH A LARGE TERMINAL DELETION 11Q21-QTER WITHOUT LOSS OF TELOMERIC SEQUENCES, AND REVIEW OF THE LITERATURE
Authors: HERTZ JM TOMMERUP N SORENSEN FB HENRIQUES UV NIELSEN A THERKELSEN AJ
Citation: Jm. Hertz et al., PARTIAL DELETION 11Q - REPORT OF A CASE WITH A LARGE TERMINAL DELETION 11Q21-QTER WITHOUT LOSS OF TELOMERIC SEQUENCES, AND REVIEW OF THE LITERATURE, Clinical genetics, 47(5), 1995, pp. 231-235
NONDISJUNCTION STUDIES IN TRISOMY-8
Authors: GRIGORIADOU M BUGGE M AVRAMOPOULOS D KITSIOUTZELI S ANNEREN G HERTZ JM LACOMBE D TSEZOU A GALLAVOUMVOURAKI A CLAUSEN N VASSILOPOULOS D BRONDUMNIELSEN K PETERSEN MB
Citation: M. Grigoriadou et al., NONDISJUNCTION STUDIES IN TRISOMY-8, American journal of human genetics, 57(4), 1995, pp. 639-639
A LINKAGE MAP OF HUMAN-CHROMOSOME-2
Authors: FLINT TJ HERTZ JM KRUSE TA
Citation: Tj. Flint et al., A LINKAGE MAP OF HUMAN-CHROMOSOME-2, Cytogenetics and cell genetics, 67(4), 1994, pp. 240-240
CHARCOT-MARIE-TOOTH DISEASE TYPE 1A - THE PARENTAL ORIGIN OF A DE-NOVO 17P11.2-P12 DUPLICATION
Authors: HERTZ JM BORGLUM AD BRANDT CA FLINT T BISGAARD C
Citation: Jm. Hertz et al., CHARCOT-MARIE-TOOTH DISEASE TYPE 1A - THE PARENTAL ORIGIN OF A DE-NOVO 17P11.2-P12 DUPLICATION, Clinical genetics, 46(4), 1994, pp. 291-294
GENETIC-MAPPING OF ALPP, CGC, COL4A3 AND COL4A4, 4 GENES LOCATED AT THE DISTAL PART OF CHROMOSOME-2Q
Authors: KRUSE TA FLINT T REEDERS ST HERTZ JM
Citation: Ta. Kruse et al., GENETIC-MAPPING OF ALPP, CGC, COL4A3 AND COL4A4, 4 GENES LOCATED AT THE DISTAL PART OF CHROMOSOME-2Q, Cytogenetics and cell genetics, 64(2), 1993, pp. 92-92
Risultati: 1-20 |