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Results: 1-25 | 26-50 | 51-55
Results: 26-50/55
GENETIC ALTERATIONS PROVIDE EVIDENCE OF CONTINUITY BETWEEN PROLIFERATIVE BREAST DISEASE (PBD) AND OVERT MALIGNANCY
Authors: WORSHAM MJ WOLMAN SR RAJU U SANFORD JS JOHNSON CC NATHANSON DS VANDYKE DL ZARBO RJ
Citation: Mj. Worsham et al., GENETIC ALTERATIONS PROVIDE EVIDENCE OF CONTINUITY BETWEEN PROLIFERATIVE BREAST DISEASE (PBD) AND OVERT MALIGNANCY, Laboratory investigation, 74(1), 1996, pp. 138-138
MOLECULAR DEFINITION OF BREAKPOINTS ASSOCIATED WITH HUMAN XQ ISOCHROMOSOMES - IMPLICATIONS FOR MECHANISMS OF FORMATION
Authors: WOLFF DJ MILLER AP VANDYKE DL SCHWARTZ S WILLARD HF
Citation: Dj. Wolff et al., MOLECULAR DEFINITION OF BREAKPOINTS ASSOCIATED WITH HUMAN XQ ISOCHROMOSOMES - IMPLICATIONS FOR MECHANISMS OF FORMATION, American journal of human genetics, 58(1), 1996, pp. 154-160
MOLECULAR CHARACTERIZATION OF DE-NOVO SECONDARY TRISOMY-13
Authors: SHAFFER LG MCCASKILL C HAN JY CUTILLO DM DONNENFELD AE WEISS L VANDYKE DL
Citation: Lg. Shaffer et al., MOLECULAR CHARACTERIZATION OF DE-NOVO SECONDARY TRISOMY-13, Cytogenetics and cell genetics, 69(1-2), 1995, pp. 115-115
CONFINED PLACENTAL MOSAICISM FOR TRISOMY-12 IN CVS WITH VARYING OUTCOMES
Authors: BISCHOFF FZ ZENGERHAIN J VANDYKE DL SHAFFER LG
Citation: Fz. Bischoff et al., CONFINED PLACENTAL MOSAICISM FOR TRISOMY-12 IN CVS WITH VARYING OUTCOMES, Cytogenetics and cell genetics, 69(1-2), 1995, pp. 118-119
MOSAICISM FOR TRISOMY-12 - 4 CASES WITH VARYING OUTCOMES
Authors: BISCHOFF FZ ZENGERHAIN J MOSES D VANDYKE DL SHAFFER LG
Citation: Fz. Bischoff et al., MOSAICISM FOR TRISOMY-12 - 4 CASES WITH VARYING OUTCOMES, Prenatal diagnosis, 15(11), 1995, pp. 1017-1026
REPLICATION BANDING AND MOLECULAR STUDIES OF A MOSAIC, UNBALANCED DIC(X-15)(XPTER-]XQ26.1 /15P11-]15QTER)/
Authors: SCHEUERLE A ZENGERHAIN JL VANDYKE DL LEDBETTER DH GREENBERG F SHAFFER LG
Citation: A. Scheuerle et al., REPLICATION BANDING AND MOLECULAR STUDIES OF A MOSAIC, UNBALANCED DIC(X-15)(XPTER-]XQ26.1 /15P11-]15QTER)/, American journal of medical genetics, 56(4), 1995, pp. 403-408
PARACENTRIC INVERSIONS IN HUMANS - A REVIEW OF 446 PARACENTRIC INVERSIONS WITH PRESENTATION OF 120 NEW CASES
Authors: PETTENATI MJ RAO PN PHELAN MC GRASS F RAO KW COSPER P CARROLL AJ ELDER F SMITH JL HIGGINS MD LANMAN JT HIGGINS RR BUTLER MG LUTHARDT F KEITGES E JACKSONCOOK C BROWN J SCHWARTZ S VANDYKE DL PALMER CG
Citation: Mj. Pettenati et al., PARACENTRIC INVERSIONS IN HUMANS - A REVIEW OF 446 PARACENTRIC INVERSIONS WITH PRESENTATION OF 120 NEW CASES, American journal of medical genetics, 55(2), 1995, pp. 171-187
COMMON CLONAL ORIGIN OF SYNCHRONOUS PRIMARY HEAD AND NECK SQUAMOUS-CELL CARCINOMAS - ANALYSIS BY TUMOR KARYOTYPES AND FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: WORSHAM MJ WOLMAN SR CAREY TE ZARBO RJ BENNINGER MS VANDYKE DL
Citation: Mj. Worsham et al., COMMON CLONAL ORIGIN OF SYNCHRONOUS PRIMARY HEAD AND NECK SQUAMOUS-CELL CARCINOMAS - ANALYSIS BY TUMOR KARYOTYPES AND FLUORESCENCE IN-SITU HYBRIDIZATION, Human pathology, 26(3), 1995, pp. 251-261
NOVEL CYTOGENETIC REARRANGEMENTS, T(11-15)(Q23-Q26) AND INV(10)(P15Q22), IN AN INFANT WITH MIXED T-CELL AND B-CELL ACUTE LYMPHOBLASTIC-LEUKEMIA
Authors: WORSHAM MJ CAMILO NA YAISH HS SHURAFA MS CAREY JL VANDYKE DL
Citation: Mj. Worsham et al., NOVEL CYTOGENETIC REARRANGEMENTS, T(11-15)(Q23-Q26) AND INV(10)(P15Q22), IN AN INFANT WITH MIXED T-CELL AND B-CELL ACUTE LYMPHOBLASTIC-LEUKEMIA, Blood, 86(10), 1995, pp. 3136-3136
INCIDENCE AND SIGNIFICANCE OF CHROMOSOME MOSAICISM INVOLVING AN AUTOSOMAL STRUCTURAL ABNORMALITY DIAGNOSED THROUGH AMNIOCENTESIS - A COLLABORATIVE STUDY
Authors: HSU LYF YU MT RICHKIND KE VANDYKE DL CRANDALL BF SAXE DS KHODR GS MENNUTI M STETTEN G MILER WA PRIEST JH
Citation: Lyf. Hsu et al., INCIDENCE AND SIGNIFICANCE OF CHROMOSOME MOSAICISM INVOLVING AN AUTOSOMAL STRUCTURAL ABNORMALITY DIAGNOSED THROUGH AMNIOCENTESIS - A COLLABORATIVE STUDY, American journal of human genetics, 57(4), 1995, pp. 259-259
IDENTIFICATION BY FISH OF A DEL(22)(Q13.3) IN A PATIENT WITH A DE-NOVO 22QS KARYOTYPE
Authors: FELDMAN GL WIKTOR A CONARD J VANDYKE DL
Citation: Gl. Feldman et al., IDENTIFICATION BY FISH OF A DEL(22)(Q13.3) IN A PATIENT WITH A DE-NOVO 22QS KARYOTYPE, American journal of human genetics, 57(4), 1995, pp. 631-631
DELETIONS OF SIMILAR-TO-12 MB OF XQ INCLUDING FMR1 RESULT IN A SEVEREPHENOTYPE IN IT MALE AND VARIABLE PHENOTYPES IN FEMALES DEPENDING OPEN THE X-INACTIVATION PATTERN
Authors: WOLFF DJ CONROY J ZURCHER V GUSTASHAW K KO L VANDYKE DL WEISS L WILLARD HF SCHWARTZ S
Citation: Dj. Wolff et al., DELETIONS OF SIMILAR-TO-12 MB OF XQ INCLUDING FMR1 RESULT IN A SEVEREPHENOTYPE IN IT MALE AND VARIABLE PHENOTYPES IN FEMALES DEPENDING OPEN THE X-INACTIVATION PATTERN, American journal of human genetics, 57(4), 1995, pp. 734-734
MAPPING OF 10Q MICROSATELLITE REPEATS USING A DE-NOVO INVERTED TANDEMDUPLICATION 10Q25-Q26.2
Authors: WORSHAM MJ VANDYKE DL JABS EW CZARNECKI P FELDMAN GL
Citation: Mj. Worsham et al., MAPPING OF 10Q MICROSATELLITE REPEATS USING A DE-NOVO INVERTED TANDEMDUPLICATION 10Q25-Q26.2, American journal of human genetics, 57(4), 1995, pp. 1904-1904
RECURRENT CYTOGENETIC ABNORMALITIES IN SQUAMOUS-CELL CARCINOMAS OF THE HEAD AND NECK REGION
Authors: VANDYKE DL WORSHAM MJ BENNINGER MS KRAUSE CJ BAKER SR WOLF GT DRUMHELLER T TILLEY BC CAREY TE
Citation: Dl. Vandyke et al., RECURRENT CYTOGENETIC ABNORMALITIES IN SQUAMOUS-CELL CARCINOMAS OF THE HEAD AND NECK REGION, Genes, chromosomes & cancer, 9(3), 1994, pp. 192-206
10P DUPLICATION CHARACTERIZED BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: WIKTOR A FELDMAN GL KRATKOCZKI P DITMARS DM VANDYKE DL
Citation: A. Wiktor et al., 10P DUPLICATION CHARACTERIZED BY FLUORESCENCE IN-SITU HYBRIDIZATION, American journal of medical genetics, 52(3), 1994, pp. 315-318
DETECTION OF 46,XX MALE BY Y-SPECIFIC WHOLE CHROMOSOME PAINT PROBE
Authors: JALAL SM LAW ME DEWALD GW SEKHON GS VANDYKE DL
Citation: Sm. Jalal et al., DETECTION OF 46,XX MALE BY Y-SPECIFIC WHOLE CHROMOSOME PAINT PROBE, American journal of medical genetics, 52(2), 1994, pp. 239-241
MOLECULAR CHARACTERIZATION OF DE-NOVO SECONDARY TRISOMY-13
Authors: SHAFFER LG MCCASKILL C HAN JY CHOO KHA CUTILLO DM DONNENFELD AE WEISS L VANDYKE DL
Citation: Lg. Shaffer et al., MOLECULAR CHARACTERIZATION OF DE-NOVO SECONDARY TRISOMY-13, American journal of human genetics, 55(5), 1994, pp. 968-974
CLONAL CYTOGENETIC EVOLUTION IN A SQUAMOUS-CELL CARCINOMA OF THE SKINFROM A XERODERMA-PIGMENTOSUM PATIENT
Authors: WORSHAM MJ CAREY TE BENNINGER MS GASSER KM KELKER W ZARBO RJ VANDYKE DL
Citation: Mj. Worsham et al., CLONAL CYTOGENETIC EVOLUTION IN A SQUAMOUS-CELL CARCINOMA OF THE SKINFROM A XERODERMA-PIGMENTOSUM PATIENT, Genes, chromosomes & cancer, 7(3), 1993, pp. 158-164
CHROMOSOMAL BIOMARKERS IN THE CLONAL EVOLUTION OF HEAD AND NECK SQUAMOUS NEOPLASIA
Authors: CAREY TE WORSHAM MJ VANDYKE DL
Citation: Te. Carey et al., CHROMOSOMAL BIOMARKERS IN THE CLONAL EVOLUTION OF HEAD AND NECK SQUAMOUS NEOPLASIA, Journal of cellular biochemistry, 1993, pp. 213-222
NONRANDOM CHROMOSOME-ABERRATIONS AND CLONAL POPULATIONS IN HEAD AND NECK-CANCER
Authors: CAREY TE VANDYKE DL WORSHAM MJ
Citation: Te. Carey et al., NONRANDOM CHROMOSOME-ABERRATIONS AND CLONAL POPULATIONS IN HEAD AND NECK-CANCER, Anticancer research, 13(6B), 1993, pp. 2561-2567
INVERTED DUPLICATION OF CHROMOSOME-5P14P15.3 CONFIRMED WITH IN-SITU HYBRIDIZATION
Authors: ZENGERHAIN JL VANDYKE DL WIKTOR A WALKER H FELDMAN GL
Citation: Jl. Zengerhain et al., INVERTED DUPLICATION OF CHROMOSOME-5P14P15.3 CONFIRMED WITH IN-SITU HYBRIDIZATION, American journal of medical genetics, 47(8), 1993, pp. 1198-1201
INVERTED DUPLICATION OF 8P - 10 NEW PATIENTS AND REVIEW OF THE LITERATURE
Authors: FELDMAN GL WEISS L PHELAN MC SCHROER RJ VANDYKE DL
Citation: Gl. Feldman et al., INVERTED DUPLICATION OF 8P - 10 NEW PATIENTS AND REVIEW OF THE LITERATURE, American journal of medical genetics, 47(4), 1993, pp. 482-486
X-INACTIVATION PATTERN IN AN ULLRICH-TURNER SYNDROME PATIENT WITH A SMALL RING-X AND NORMAL INTELLIGENCE
Authors: ZENGERHAIN JL WIKTOR A GOLDMAN J VANDYKE DL WEISS L
Citation: Jl. Zengerhain et al., X-INACTIVATION PATTERN IN AN ULLRICH-TURNER SYNDROME PATIENT WITH A SMALL RING-X AND NORMAL INTELLIGENCE, American journal of medical genetics, 47(4), 1993, pp. 490-493
INTERSTITIAL DELETION OF CHROMOSOME-10, DEL(10) (Q11.2Q22.1) IN A BOYWITH DEVELOPMENTAL DELAY AND MULTIPLE CONGENITAL-ANOMALIES
Authors: ZENGERHAIN JL ROBERSON J VANDYKE DL WEISS L
Citation: Jl. Zengerhain et al., INTERSTITIAL DELETION OF CHROMOSOME-10, DEL(10) (Q11.2Q22.1) IN A BOYWITH DEVELOPMENTAL DELAY AND MULTIPLE CONGENITAL-ANOMALIES, American journal of medical genetics, 46(4), 1993, pp. 438-440
DEFICIENT TRANSCRIPTION OF XIST FROM TINY RING X-CHROMOSOMES IN FEMALES WITH SEVERE PHENOTYPES
Authors: MIGEON BR LUO SY STASIOWSKI BA JANI M AXELMAN J VANDYKE DL WEISS L JACOBS PA YANGFENG TL WILEY JE
Citation: Br. Migeon et al., DEFICIENT TRANSCRIPTION OF XIST FROM TINY RING X-CHROMOSOMES IN FEMALES WITH SEVERE PHENOTYPES, Proceedings of the National Academy of Sciences of the United Statesof America, 90(24), 1993, pp. 12025-12029
Risultati: 1-25 | 26-50 | 51-55