A multicenter investigation with interphase fluorescence in situ hybridization using X- and Y-chromosome probes

American Journal of Medical Genetics

Volumn 76, Issue 4, 1998, Pages 318-326

  Dewald, Gordon ^a   Stallard, Richard ^b   Saadi, A A I ^c   Arnold, Susan ^d   Bader, Patricia I ^e   Blough, Ruthann ^f   Chen, Kathy ^g   Rafael Elejalde B ^h   Harris, Catherine J ⁱ   Higgins, Rodney R ^j   Hoeltge, Gerald A ^k   Hsu, Wei Tong ^l   Kubic, Virginia ^m   James McCorquodale, D ⁿ   Micale, Mark A ^a   Moore, J W ^e   Phillips, Rosalie M ^e   Scheib Wixted, Susan ^c   Schwartz, Stuart ^e   Siembieda, Steven ^e   Strole, Kathy ^c   Vantuinen, Peter ^e   Vance, Gail H ^c   Wiktor, Ann ^a   Wise, Laura ^a   Yung, Jar Fee ^c   Zenger Hain, Julie ^e   Zinsmeister, Alan ^a   more..

^a MAYO CLINIC   (United States)

^b UNIVERSITY OF WISCONSIN MADISON   (United States)

^c WILLIAM BEAUMONT HOSPITAL   (United States)

^d AKRON CHILDREN'S HOSPITAL   (United States)

^e Parkview Hospital   (United States)

^f CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

^g ADVOCATE LUTHERAN GENERAL HOSPITAL   (United States)

^h Medical Genetics Institute   (United States)

ⁱ Wisconsin   (United States)

^j Jr Hospital of Cook County   (United States)

^k Allina Hospitals & Clinics   (United States)

^l LERNER RESEARCH INSTITUTE   (United States)

^m RUSH UNIVERSITY MEDICAL CENTER   (United States)

ⁿ HENNEPIN COUNTY MEDICAL CENTER   (United States)

more..

Author keywords

Analytical sensitivity; Chimerism; Clone; Interphase fluorescence in situ hybridization; Mosaicism; Quality assurance; Workload; X and Y chromosome probes

Indexed keywords

LEUKOAGGLUTININ;

ARTICLE; CHIMERA; CHROMOSOME ANALYSIS; CHROMOSOME MOSAICISM; DIAGNOSTIC VALUE; DNA PROBE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN EXPERIMENT; INTERPHASE; MALE; METAPHASE CHROMOSOME; NORMAL HUMAN; PRIORITY JOURNAL; X CHROMOSOME; Y CHROMOSOME;

CYTOGENETICS; DNA PROBES; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INTERPHASE; LABORATORIES; LYMPHOCYTE ACTIVATION; LYMPHOCYTES; MALE; METAPHASE; PHYTOHEMAGGLUTININS; QUALITY CONTROL; REPRODUCIBILITY OF RESULTS; SENSITIVITY AND SPECIFICITY; WORKLOAD; X CHROMOSOME; Y CHROMOSOME;

PHASEOLUS VULGARIS;

EID: 18344403136     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980401)76:4<318::AID-AJMG7>3.0.CO;2-L     Document Type: Article

References (14)

1. American College of Medical Genetics (1996): "Standards and Guidelines: Clinical Genetic Laboratories, Supplement 1." Bethesda, MD: The American College of Medical Genetics Laboratory Practice Committee.
2. Bryant E, Patil SR, Theil K, Seelig S, Hsu P (1995): Reproducibility of Spectrum CEP X/Y dual color probe kit for enumeration of XX and XY cells in opposite-sex bone marrow transplant patients: A multicenter clinical validation study. Am J Hum Genet 57(A109):607.
3. Dewald GW, Schad CR, Christensen ER, Tiède AL, Zinsmeister AR, Spurbeck JL, Thibodeau S, Jalal JM (1993a): The application of fluorescent in situ hybridization to detect Mbcr/abl fusion in variant Ph chromosomes in CML and ALL. Cancer Genet Cytogenet 71:7-14.
4. Dewald GW, Schad CR, Christensen ER, Lav ME, Zinsmeister AR, Stalboerger PG, Jalal SM, Ash RC, Jenkins RB (1993b): Fluorescent in situ hybridization with X and Y chromosome probes for cytogenetic study on bone marrow cells after opposite sex transplantation. Bone Marrow Transplant 12:149-154.
5. Dewald GW, Stallard R, Bader PI, Chen K, Zenger-Hain J, Harris CJ, Higgins R, Hirsch 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, Van Tuninen P, Wiktor A, Yung JF (1996): Toward quality assurance for metaphase FISH: A multicenter experience. Am J Med Genet 65:1-8.
6. Dewald GW, Brothman AR, Butler MG, Cooley LD, Patil SR, Saikevych IA, Schneider NR (1997): Pilot studies for proficiency testing using fluorescence in situ hybridization with chromosome-specific DNA probes. Arch Pathol Lab Med 121:359-367.
7. ISCN (1995): "An International System for Human Cytogenetic Nomenclature." Mitelman F (ed): Basel: S. Karger.
8. Jenkins RB, Le Beau MM, Kraker WS, Borell TJ, Stalboerger PG, Davis EM, Penland L (1992): Fluorescence in situ hybridization: A sensitive method for trisomy 8 detection in bone marrow specimens. Blood 79: 3307-3315.
9. Koska R (1997): CEP 8, CEP 12 and CEP X/Y DNA probe kits first FDA cleared products utilizing FISH technology. Vysions 2:6-7.
10. Lu PY, Hammitt DG, Zinsmeister AR, Dewald GW (1994): Dual color fluorescence in situ hybridization to investigate aneuploidy in sperm from 33 normal males and a man with a t(2;4;8Xq23;q27;p21). Fertil Steril 62:394-396.
11. Patil SR, Bryant E, Theil K, Seelig S, Hsu P (1995): Accuracy of spectrum CEP X/Y dual color probe kit for detection of XX and XY cells in opposite-sex bone marrow transplant patients: A multicenter clinical validation study. Am J Hum Genet 57(A74):397.
12. Schad CR, Dewald GW (1995): Building a new clinical test for fluorescence in situ hybridization. Appl Cytogenet 21:1-4.
13. Spurbeck JL, Zinsmeister AR, Meyer KJ, Jalal SM (1996): The dynamics of chromosome spreading. Am J Med Genet 61:387-393.
14. Trask B (1991): Fluorescence in situ hybridization: Applications in cytogenetics and gene mapping. Technical Focus 7:149-154.