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Results: 1-25 | 26-45
Results: 1-25/45
CHROMOSOMAL-ABNORMALITIES IN NODAL AND EXTRANODAL CD30-CELL LYMPHOMAS- INFREQUENT DETECTION OF THE T(2-5) IN EXTRANODAL LYMPHOMAS( ANAPLASTIC LARGE)
Authors: OTT G KATZENBERGER T SIEBERT R DECOTEAU JF FLETCHER JA KNOLL JHM KALLA J ROSENWALD A OTT MM WEBERMATTHIESEN K KADIN ME MULLERHERMELINK HK
Citation: G. Ott et al., CHROMOSOMAL-ABNORMALITIES IN NODAL AND EXTRANODAL CD30-CELL LYMPHOMAS- INFREQUENT DETECTION OF THE T(2-5) IN EXTRANODAL LYMPHOMAS( ANAPLASTIC LARGE), Genes, chromosomes & cancer, 22(2), 1998, pp. 114-121
PHYSICAL AND LINKAGE MAPPING OF THE GENE FOR THE ALPHA-3 CHAIN OF TYPE-IX COLLAGEN, COL9A3, TO HUMAN-CHROMOSOME 20Q13.3
Authors: TILLER GE WARMAN ML GONG Y KNOLL JHM MAYNE R BREWTON RG
Citation: Ge. Tiller et al., PHYSICAL AND LINKAGE MAPPING OF THE GENE FOR THE ALPHA-3 CHAIN OF TYPE-IX COLLAGEN, COL9A3, TO HUMAN-CHROMOSOME 20Q13.3, Cytogenetics and cell genetics, 81(3-4), 1998, pp. 205-207
EXCLUSION OF UNIPARENTAL INHERITANCE OF CHROMOSOME-15 IN A FETUS WITHA FAMILIAL DICENTRIC (Y-15) TRANSLOCATION
Authors: WHITE LM TREAT K LEFF A STYERS D MITCHELL M KNOLL JHM
Citation: Lm. White et al., EXCLUSION OF UNIPARENTAL INHERITANCE OF CHROMOSOME-15 IN A FETUS WITHA FAMILIAL DICENTRIC (Y-15) TRANSLOCATION, Prenatal diagnosis, 18(2), 1998, pp. 111-116
INTERSTITIAL DUPLICATIONS OF CHROMOSOME REGION 15Q11Q13 - CLINICAL AND MOLECULAR CHARACTERIZATION
Authors: REPETTO GR WHITE LM BADER PJ JOHNSON D KNOLL JHM
Citation: Gr. Repetto et al., INTERSTITIAL DUPLICATIONS OF CHROMOSOME REGION 15Q11Q13 - CLINICAL AND MOLECULAR CHARACTERIZATION, American journal of medical genetics, 79(2), 1998, pp. 82-89
COMPLEX FAMILIAL REARRANGEMENT OF CHROMOSOME 9P24.3 DETECTED BY FISH
Authors: REPETTO GM WAGSTAFF J KORF BR KNOLL JHM
Citation: Gm. Repetto et al., COMPLEX FAMILIAL REARRANGEMENT OF CHROMOSOME 9P24.3 DETECTED BY FISH, American journal of medical genetics, 76(4), 1998, pp. 306-309
LIMATIN (LIMAB1), AN ACTIN-BINDING LIM PROTEIN, MAPS TO MOUSE-CHROMOSOME-19 AND HUMAN-CHROMOSOME 10Q25, A REGION FREQUENTLY DELETED IN HUMAN CANCERS
Authors: KIM AC PETERS LL KNOLL JHM VANHUFFEL C CICIOTTE SL KLEYN PW CHISHTI AH
Citation: Ac. Kim et al., LIMATIN (LIMAB1), AN ACTIN-BINDING LIM PROTEIN, MAPS TO MOUSE-CHROMOSOME-19 AND HUMAN-CHROMOSOME 10Q25, A REGION FREQUENTLY DELETED IN HUMAN CANCERS, Genomics, 46(2), 1997, pp. 291-293
MOLECULAR CHARACTERIZATION AND LOCALIZATION OF THE HUMAN MAFG GENE
Authors: BLANK V KNOLL JHM ANDREWS NC
Citation: V. Blank et al., MOLECULAR CHARACTERIZATION AND LOCALIZATION OF THE HUMAN MAFG GENE, Genomics, 44(1), 1997, pp. 147-149
COMPLETE PRIMARY STRUCTURE OF 2 SPLICE VARIANTS OF COLLAGEN-XII, AND ASSIGNMENT OF ALPHA-1(XII) COLLAGEN (COL12A1), ALPHA-1(IX) COLLAGEN (COL9A1), AND ALPHA-1(XIX) COLLAGEN (COL19A1) TO HUMAN-CHROMOSOME 6Q12-Q13
Authors: GERECKE DR OLSON PF KOCH M KNOLL JHM TAYLOR R HUDSON DL CHAMPLIAUD MF OLSEN BR BURGESON RE
Citation: Dr. Gerecke et al., COMPLETE PRIMARY STRUCTURE OF 2 SPLICE VARIANTS OF COLLAGEN-XII, AND ASSIGNMENT OF ALPHA-1(XII) COLLAGEN (COL12A1), ALPHA-1(IX) COLLAGEN (COL9A1), AND ALPHA-1(XIX) COLLAGEN (COL19A1) TO HUMAN-CHROMOSOME 6Q12-Q13, Genomics, 41(2), 1997, pp. 236-242
DETECTION OF THE T(2-5)(P23-Q35) IN NODAL AND PRIMARY EXTRANODAL CD30-CELL LYMPHOMAS( ANAPLASTIC LARGE)
Authors: KALLA J OTT G KATZENBERGER T FLETCHER JA KNOLL JHM ROSENWALD A DECOTEAU JF SIEBERT R OTT MM KADIN ME MULLERHERMELINK HK
Citation: J. Kalla et al., DETECTION OF THE T(2-5)(P23-Q35) IN NODAL AND PRIMARY EXTRANODAL CD30-CELL LYMPHOMAS( ANAPLASTIC LARGE), Cytogenetics and cell genetics, 77(1-2), 1997, pp. 321-321
RELAXATION OF IMPRINTING IN PATIENTS WITH PRADER-WILLI-SYNDROME
Authors: ROGAN PK SEIP JR KNOLL JHM WHITE LM WENGER SL STEELE MW SPERLING MA APARICIO L MENON R
Citation: Pk. Rogan et al., RELAXATION OF IMPRINTING IN PATIENTS WITH PRADER-WILLI-SYNDROME, American journal of medical genetics, 73(4), 1997, pp. 2-2
MUTATIONS INVOLVING THE TRANSCRIPTION FACTOR CBFA1 CAUSE CLEIDOCRANIAL DYSPLASIA
Authors: MUNDLOS S OTTO F MUNDLOS C MULLIKEN JB AYLSWORTH AS ALBRIGHT S LINDHOUT D COLE WG HENN W KNOLL JHM OWEN MJ MERTELSMANN R ZABEL BU OLSEN BR
Citation: S. Mundlos et al., MUTATIONS INVOLVING THE TRANSCRIPTION FACTOR CBFA1 CAUSE CLEIDOCRANIAL DYSPLASIA, Cell, 89(5), 1997, pp. 773-779
46,XX, INV(6)(P21.1P23) IN A PEDIGREE WITH HEREDITARY HEMOCHROMATOSIS
Authors: VENDITTI CP SEESE NK GERHARD GS TENELSHOF AE CHORNEY KA MOWREY PN LACEY PG KNOLL JHM CHORNEY MJ
Citation: Cp. Venditti et al., 46,XX, INV(6)(P21.1P23) IN A PEDIGREE WITH HEREDITARY HEMOCHROMATOSIS, Journal of Medical Genetics, 34(1), 1997, pp. 24-27
AN ISOTYPE-SPECIFIC ACTIVATOR OF MAJOR HISTOCOMPATIBILITY COMPLEX (MHC) CLASS-II GENES THAT IS INDEPENDENT OF CLASS-II TRANSACTIVATOR
Authors: DOUHAN J LIEBERSON R KNOLL JHM ZHOU H GLIMCHER LH
Citation: J. Douhan et al., AN ISOTYPE-SPECIFIC ACTIVATOR OF MAJOR HISTOCOMPATIBILITY COMPLEX (MHC) CLASS-II GENES THAT IS INDEPENDENT OF CLASS-II TRANSACTIVATOR, The Journal of experimental medicine, 185(11), 1997, pp. 1885-1895
INTERSTITIAL DUPLICATION OF PROXIMAL CHROMOSOME 15Q IN 3 PATIENTS WITH AUTISTIC FEATURES AND MENTAL-RETARDATION
Authors: REPETTO GM WHITE LM BADER PJ JOHNSON D KNOLL JHM
Citation: Gm. Repetto et al., INTERSTITIAL DUPLICATION OF PROXIMAL CHROMOSOME 15Q IN 3 PATIENTS WITH AUTISTIC FEATURES AND MENTAL-RETARDATION, American journal of human genetics, 61(4), 1997, pp. 790-790
PHYSICAL AND LINKAGE MAPPING OF THE GENE FOR THE ALPHA-3 CHAIN OF TYPE-IX COLLAGEN, COL9A3, TO HUMAN-CHROMOSOME 20Q13.3
Authors: TILLER GE WARMAN ML GONG Y KNOLL JHM MAYNE R BREWTON RG
Citation: Ge. Tiller et al., PHYSICAL AND LINKAGE MAPPING OF THE GENE FOR THE ALPHA-3 CHAIN OF TYPE-IX COLLAGEN, COL9A3, TO HUMAN-CHROMOSOME 20Q13.3, American journal of human genetics, 61(4), 1997, pp. 1735-1735
A GENE FOR ISOLATED CONGENITAL PTOSIS MAPS TO A 3-CM REGION WITHIN 1P32-P34.1
Authors: ENGLE EC CASTRO AE MACY ME KNOLL JHM BEGGS AH
Citation: Ec. Engle et al., A GENE FOR ISOLATED CONGENITAL PTOSIS MAPS TO A 3-CM REGION WITHIN 1P32-P34.1, American journal of human genetics, 60(5), 1997, pp. 1150-1157
ANGELMAN SYNDROME-ASSOCIATED WITH AN INVERSION OF CHROMOSOME 15Q11.2Q24.3
Authors: GREGER V KNOLL JHM WAGSTAFF J WOOLF E LIESKE P GLATT H BENN PA ROSENGREN SS LALANDE M
Citation: V. Greger et al., ANGELMAN SYNDROME-ASSOCIATED WITH AN INVERSION OF CHROMOSOME 15Q11.2Q24.3, American journal of human genetics, 60(3), 1997, pp. 574-580
ALLELE-SPECIFIC REPLICATION OF 15Q11-Q13 LOCI - A DIAGNOSTIC-TEST FORDETECTION OF UNIPARENTAL DISOMY
Authors: WHITE LM ROGAN PK NICHOLLS RD WU BL KORF B KNOLL JHM
Citation: Lm. White et al., ALLELE-SPECIFIC REPLICATION OF 15Q11-Q13 LOCI - A DIAGNOSTIC-TEST FORDETECTION OF UNIPARENTAL DISOMY, American journal of human genetics, 59(2), 1996, pp. 423-430
DIAGNOSTIC TESTING FOR PRADER-WILLI AND ANGELMAN SYNDROMES - REPORT OF THE ASHC ACMC TEST AND TECHNOLOGY-TRANSFER COMMITTEE/
Authors: CASSIDY SB BEAUDET AL KNOLL JHM LEDBETTER DH NICHOLLS RD SCHWARTZ S BUTLER MG WATSON M
Citation: Sb. Cassidy et al., DIAGNOSTIC TESTING FOR PRADER-WILLI AND ANGELMAN SYNDROMES - REPORT OF THE ASHC ACMC TEST AND TECHNOLOGY-TRANSFER COMMITTEE/, American journal of human genetics, 58(5), 1996, pp. 1085-1088
HDLG - CHROMOSOME LOCATION OF THE CLOSEST HUMAN HOMOLOG OF THE DROSOPHILA DISCS LARGE TUMOR-SUPPRESSOR GENE
Authors: AZIM AC KNOLL JHM MARFATIA SM LIN L PEEL D BRYANT PJ CHISHTI AH
Citation: Ac. Azim et al., HDLG - CHROMOSOME LOCATION OF THE CLOSEST HUMAN HOMOLOG OF THE DROSOPHILA DISCS LARGE TUMOR-SUPPRESSOR GENE, Molecular biology of the cell, 6, 1995, pp. 1574-1574
GENETIC-MAPPING OF CLEIDOCRANIAL DYSPLASIA AND EVIDENCE OF A MICRODELETION IN ONE FAMILY
Authors: MUNDLOS S MULLIKEN JB ABRAMSON DL WARMAN ML KNOLL JHM OLSEN BR
Citation: S. Mundlos et al., GENETIC-MAPPING OF CLEIDOCRANIAL DYSPLASIA AND EVIDENCE OF A MICRODELETION IN ONE FAMILY, Human molecular genetics, 4(1), 1995, pp. 71-75
DLG1 - CHROMOSOME LOCATION OF THE CLOSEST HUMAN HOMOLOG OF THE DROSOPHILA DISCS LARGE TUMOR-SUPPRESSOR GENE
Authors: AZIM AC KNOLL JHM MARFATIA SM PEEL DJ BRYANT PJ CHISHTI AH
Citation: Ac. Azim et al., DLG1 - CHROMOSOME LOCATION OF THE CLOSEST HUMAN HOMOLOG OF THE DROSOPHILA DISCS LARGE TUMOR-SUPPRESSOR GENE, Genomics, 30(3), 1995, pp. 613-616
THE OXYTOCIN RECEPTOR GENE (OXTR) LOCALIZES TO HUMAN-CHROMOSOME 3P25 BY FLUORESCENCE IN-SITU HYBRIDIZATION AND PCR ANALYSIS OF SOMATIC-CELLHYBRIDS
Authors: SIMMONS CF CLANCY TE QUAN R KNOLL JHM
Citation: Cf. Simmons et al., THE OXYTOCIN RECEPTOR GENE (OXTR) LOCALIZES TO HUMAN-CHROMOSOME 3P25 BY FLUORESCENCE IN-SITU HYBRIDIZATION AND PCR ANALYSIS OF SOMATIC-CELLHYBRIDS, Genomics, 26(3), 1995, pp. 623-625
THE GAMMA-AMINOBUTYRIC-ACID RECEPTOR GAMMA-3 SUBUNIT GENE (GABRG3) ISTIGHTLY LINKED TO THE ALPHA-5 SUBUNIT GENE (GABRA5) ON HUMAN-CHROMOSOME 15Q11-Q13 AND IS TRANSCRIBED IN THE SAME ORIENTATION
Authors: GREGER V KNOLL JHM WOOLF E GLATT K TYNDALE RF DELOREY TM OLSEN RW TOBIN AJ SIKELA JM NAKATSU Y BRILLIANT MH WHITING PJ LALANDE M
Citation: V. Greger et al., THE GAMMA-AMINOBUTYRIC-ACID RECEPTOR GAMMA-3 SUBUNIT GENE (GABRG3) ISTIGHTLY LINKED TO THE ALPHA-5 SUBUNIT GENE (GABRA5) ON HUMAN-CHROMOSOME 15Q11-Q13 AND IS TRANSCRIBED IN THE SAME ORIENTATION, Genomics, 26(2), 1995, pp. 258-264
CYTOGENETIC FINDINGS IN REGRESSING SKIN-LESIONS OF LYMPHOMATOID PAPULOSIS
Authors: PETERS K KNOLL JHM KADIN ME
Citation: K. Peters et al., CYTOGENETIC FINDINGS IN REGRESSING SKIN-LESIONS OF LYMPHOMATOID PAPULOSIS, Cancer genetics and cytogenetics, 80(1), 1995, pp. 13-16
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