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Results: 1-13 |
Results: 13
SEQUENTIAL G-BANDING AND FLUORESCENT IN-SITU HYBRIDIZATION ON PERIPHERAL-BLOOD, BONE-MARROW, AND AMNIOTIC-FLUID SAMPLES
Authors: WIKTOR A PUSKORIUS R ZUBRICKAS K VANDYKE DL
Citation: A. Wiktor et al., SEQUENTIAL G-BANDING AND FLUORESCENT IN-SITU HYBRIDIZATION ON PERIPHERAL-BLOOD, BONE-MARROW, AND AMNIOTIC-FLUID SAMPLES, American journal of medical genetics, 79(1), 1998, pp. 38-41
A MULTICENTER INVESTIGATION WITH INTERPHASE FLUORESCENCE IN-SITU HYBRIDIZATION USING X-CHROMOSOME AND Y-CHROMOSOME PROBES
Authors: DEWALD G STALLARD R ALSAADI A ARNOLD S BADER PI BLOUGH R CHEN K ELEJALDE BR HARRIS CJ HIGGINS RR HOELTGE GA HSU WT KUBIC V MCCORQUODALE DJ MICALE MA MOORE JW PHILLIPS RM SCHEIBWIXTED S SCHWARTZ S SIEMBIEDA S STROLE K VANTUINEN P VANCE GH WIKTOR A WISE L YUNG JF ZENGERHAIN J ZINSMEISTER A
Citation: G. Dewald et al., A MULTICENTER INVESTIGATION WITH INTERPHASE FLUORESCENCE IN-SITU HYBRIDIZATION USING X-CHROMOSOME AND Y-CHROMOSOME PROBES, American journal of medical genetics, 76(4), 1998, pp. 318-326
CYTOGENETIC AND CLINICAL FINDINGS IN A PATIENT WITH A DELETION OF 16Q23.1 - FIRST REPORT OF BILATERAL CATARACTS AND A 16Q DELETION
Authors: MONAGHAN KG VANDYKE DL WIKTOR A FELDMAN GL
Citation: Kg. Monaghan et al., CYTOGENETIC AND CLINICAL FINDINGS IN A PATIENT WITH A DELETION OF 16Q23.1 - FIRST REPORT OF BILATERAL CATARACTS AND A 16Q DELETION, American journal of medical genetics, 73(2), 1997, pp. 180-183
IMMUNOPHENOTYPING, CYTOGENETICS AND MOLECULAR ANALYSES AS TOOLS FOR REFINING CLL PHENOTYPES
Authors: SHURAFA M VANDYKE D BARNABAS N MAEDA K HAWLEY R CLARK D WIKTOR A GASSER K WORSHAM M
Citation: M. Shurafa et al., IMMUNOPHENOTYPING, CYTOGENETICS AND MOLECULAR ANALYSES AS TOOLS FOR REFINING CLL PHENOTYPES, Blood, 90(10), 1997, pp. 3735-3735
DIAGNOSTIC TESTING - A COST-ANALYSIS FOR PRADER-WILLI AND ANGELMAN SYNDROMES
Authors: MONAGHAN KG VANDYKE DL FELDMAN G WIKTOR A WEISS L
Citation: Kg. Monaghan et al., DIAGNOSTIC TESTING - A COST-ANALYSIS FOR PRADER-WILLI AND ANGELMAN SYNDROMES, American journal of human genetics, 60(1), 1997, pp. 244-247
TOWARD QUALITY ASSURANCE FOR METAPHASE FISH - A MULTICENTER EXPERIENCE
Authors: DEWALD G STALLARD R BADER PI CHEN K ZENGERHAIN J HARRIS CJ HIGGINS R HIRSCH B HSU WT JOHNSON E KUBIC V KURCZYNSKI TW MALONE JM MCCORQUODALE DJ MEILINGER K MEISNER LF MOORE JW SCHWARTZ S SIEMBIEDA S STORTO PD VANCE G VANTUINEN P WIKTOR A YUNG JF
Citation: G. Dewald et al., TOWARD QUALITY ASSURANCE FOR METAPHASE FISH - A MULTICENTER EXPERIENCE, American journal of medical genetics, 64(4), 1996, pp. 539-545
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
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
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
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
FLUORESCENT IN-SITU HYBRIDIZATION TO CHARACTERIZE UNBALANCED CHROMOSOME REARRANGEMENTS - 10P DUPLICATION
Authors: WIKTOR A FELDMAN GL VANDYKE DL
Citation: A. Wiktor et al., FLUORESCENT IN-SITU HYBRIDIZATION TO CHARACTERIZE UNBALANCED CHROMOSOME REARRANGEMENTS - 10P DUPLICATION, American journal of human genetics, 53(3), 1993, pp. 626-626
TWINS WITH A DE-NOVO 46,X,DER(X)T(X Y)(P22.3 Q11.2) AND NORMAL PHENOTYPE - IN-SITU AND MOLECULAR-X STUDIES
Authors: ZENGERHAIN J WIKTOR A VATS S BALLABIO A GRILLO A VANDYKE DL WEISS L
Citation: J. Zengerhain et al., TWINS WITH A DE-NOVO 46,X,DER(X)T(X Y)(P22.3 Q11.2) AND NORMAL PHENOTYPE - IN-SITU AND MOLECULAR-X STUDIES, American journal of human genetics, 53(3), 1993, pp. 631-631
APPLICATION OF FISH FOR RAPID ANEUPLOIDY SCREENING OF CVS
Authors: VATS S WIKTOR A ZENGERHAIN JL VANDYKE DL WEISS L
Citation: S. Vats et al., APPLICATION OF FISH FOR RAPID ANEUPLOIDY SCREENING OF CVS, American journal of human genetics, 53(3), 1993, pp. 1469-1469
Risultati: 1-13 |