98 Publications (Page 4 of 4)
2001
Improvements in cytogenetic slide preparation: Controlled chromosome spreading, chemical aging and gradual denaturing
Henegariu, OctavianHeerema, Nyla ALowe Wright, LisaBray‐Ward, PatriciaWard, David C and Vance, Gail H
Cytometry, vol. 43, (no. 2), pp. 109, 1 February 2001. | Journal Article
 
Validation of Scales to Measure Benefits of and Barriers to Colorectal Cancer Screening
Rawl, Susan MRawl, SusanChampion, Victoria LChampion, VictoriaMenon, UshaMenon, UshaLoehrer, Patrick JLoehrer, Patrick JVance, Gail HVance, Gail HSkinner, Celette S and Skinner, Celette Sugg
Journal of Psychosocial Oncology, vol. 19, (no. 3-4), pp. 63, 12/3/2001. | Journal Article
1999
De novo 10q22 interstitial deletion.
Cook, LWeaver, David DHartsfield, James K and Vance, Gail H
Journal of medical genetics, vol. 36, (no. 1), pp. 71-2, 1999/Jan. | Journal Article
 
Detection of Monosomy 7 in Bone Marrow by Fluorescence In Situ Hybridization
Thurston, Virginia CCeperich, Tina MVance, Gail H and Heerema, Nyla A
Cancer Genetics and Cytogenetics, vol. 109, (no. 2), pp. 160, 1999-03-00. | Journal Article
 
Detection of monosomy 7 in bone marrow by fluorescence in situ hybridization. A study of Fanconi anemia patients and review of the literature.
Thurston, Virginia CCeperich, T MVance, Gail H and Heerema, N A
Cancer genetics and cytogenetics, vol. 109, (no. 2), pp. 154-60, 1999/Mar. | Journal Article
 
Detection of Mosaicism in amniotic fluid cultures: A CYT02000 collaborative study
Ing, Paul SVan Dyke, Daniel LCaudill, Samuel PReidy, John ABice, GillianBieber, Frederick RBuchanan, Phillip DCarroll, Andrew JCheung, Sau WDewald, GordonDonahue, Roger PGardner, H AllenHiggins, JamesHsu, Lillian YeJamehdor, MehdiKeitges, Elisabeth ALaundon, Caroline HLuthardt, Frederick WMascarello, JamesMay, Kristin MMeck, Jeanne MMorton, CynthiaPatil, ShivaPeakman, DavidPettenati, Mark JRao, NageshSanger, Warren GSaxe, Deborah FSchwartz, StuartSekhon, Gurbax SVance, Gail HWyandt, Herman EYu, Cheng WZenger-Hain, Julie and L. Chen, Andrew T
Genetics in Medicine, vol. 1, (no. 3), pp. 97, 1999-04-00. | Journal Article
 
Detection of mosaicism in amniotic fluid cultures: a CYTO2000 collaborative study.
Ing, P SVan Dyke, Daniel LCaudill, S PReidy, J ABice, GBieber, Frederick RBuchanan, P DCarroll, A JCheung, Steven WDewald, Gordon WDonahue, R PGardner, H AHiggins, JHsu, L YJamehdor, MKeitges, E ALaundon, C HLuthardt, F WMascarello, JMay, K MMeck, J MMorton, Cynthia CPatil, SPeakman, DPettenati, M JRao, NSanger, W GSaxe, D FSchwartz, SSekhon, G SVance, Gail HWyandt, H EYu, Cheng WZenger-Hain, J and Chen, A T
Genetics in medicine : official journal of the American College of Medical Genetics, vol. 1, (no. 3), pp. 94-7, 1999 Mar-Apr. | Journal Article
1998
A multicenter investigation with interphase fluorescence in situ hybridization using X‐ and Y‐chromosome probes
Dewald, Gordon WDewald, GordonStallard, RichardStallard, RAl Saadi, ASaadi, A. AlArnold, SusanArnold, SBader, Patricia IBader, P IBlough, RBlough, RuthannChen, KChen, KathyElejalde, B. RafaelElejalde, B RHarris, Catherine JHarris, C JHiggins, R RHiggins, Rodney RHoeltge, G AHoeltge, Gerald AHsu, Wei‐TongHsu, W TKubic, VirginiaKubic, VMcCorquodale, D. JamesMcCorquodale, D JMicale, Mark AMicale, M AMoore, J WMoore, J.WPhillips, R MPhillips, Rosalie MScheib-Wixted, SScheib‐Wixted, SusanSchwartz, SSchwartz, StuartSiembieda, StevenSiembieda, SStrole, KathyStrole, KVanTuinen, PeterVanTuinen, PVance, G HVance, Gail HWiktor, AWiktor, AnnZinsmeister, AWise, LauraYung, Jar‐FeeZenger‐Hain, Julie and Zinsmeister, Alan
American Journal of Medical Genetics, vol. 76, (no. 4), pp. 326, 1 April 1998. | Journal Article
 
Characterization of Multiple 12p Rearrangements in Testicular Germ Cell Tumor Cell Line 833K and Its Subclone 64CP by Chromosome Microdissection
Blough, Ruthann IVance, Gail HHenegariu, OctavianSmolarek, Teresa ASledge, George W and Heerema, Nyla A
Cancer Genetics and Cytogenetics, vol. 106, (no. 1), pp. 29, 1998. | Journal Article
 
Cytogenetics: a short review and update.
Vance, Gail H
Cancer Investigation, vol. 16, (no. 1), pp. 40-4, 1998. | Journal Article
 
Molecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7q.
Vance, Gail HNickerson, CSarnat, LZhang, AHenegariu, OMorichon-Delvallez, NButler, Merlin G and Palmer, C G
American journal of medical genetics, vol. 76, (no. 1), pp. 51-7, 1998/Feb/26. | Journal Article
 
Partners with reciprocal translocations: genetic counseling for the ‘double translocation’
Cook, LCook, LolaHartsfield, James KHartsfield, James KVance, G H and Vance, Gail H
Clinical Genetics, vol. 53, (no. 5), pp. 407, May 1998. | Journal Article
 
Triple-color FISH analysis of 12p amplification in testicular germ-cell tumors using 12p band-specific painting probes
Henegariu, OVance, Gail HHeiber, DevanPera, Martin and Heerema, Nyla A
Journal of Molecular Medicine, vol. 76, (no. 9), pp. 655, 19980700. | Journal Article
 
Variable phenotype of familial adenomatous polyposis in pedigrees with 3' mutation in the APC gene.
Brensinger, J DLaken, S JLuce, M CPowell, Steven MVance, Gail HAhnen, D JPetersen, G MHamilton, Stanley R and Giardiello, Francis M
Gut, vol. 43, (no. 4), pp. 548-52, 1998/Oct. | Journal Article
1997
A case with mosaic di-, tetra-, and octacentric ring Y chromosomes.
Henegariu, OPescovitz, O HVance, Gail HVerbrugge, J and Heerema, N A
American journal of medical genetics, vol. 71, (no. 4), pp. 426-9, 1997/Sep/5. | Journal Article
 
An apparently acentric marker chromosome originating from 9p with a functional centromere without detectable alpha and beta satellite sequences.
Vance, Gail HCurtis, C AHeerema, N ASchwartz, S and Palmer, C G
American journal of medical genetics, vol. 71, (no. 4), pp. 436-42, 1997/Sep/5. | Journal Article
 
Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA
Depinet, TWZackowski, JLEarnshaw, William CKaffe, S.Sekhon, GSStallard, R.Sullivan, Beth AVance, Gail HVan Dyke, Daniel LWillard, Huntington FZinn, AB and Schwartz, S.
Human Molecular Genetics, vol. 6, (no. 8), pp. 1195-1204, 1997. | Journal Article
 
Mild "duplication 6q syndrome": a case with partial trisomy (6)(q23.3q25.3).
Henegariu, OHeerema, N A and Vance, Gail H
American journal of medical genetics, vol. 68, (no. 4), pp. 450-4, 1997/Feb/11. | Journal Article
 
Urorectal septum malformation sequence: Report of thirteen additional cases and review of the literature
Wheeler, Patricia GWheeler, Patricia GWeaver, David DWeaver, David DObeime, Mercy OObeime, Mercy OVance, Gail HVance, Gail HBull, Marilyn JBull, Marilyn JEscobar, Luis F and Escobar, Luis F
American Journal of Medical Genetics, vol. 73, (no. 4), pp. 462, 31 December 1997. | Journal Article
1996
Dicentric (9;20)(p11;q11) identified by fluorescence in situ hybridization in four pediatric acute lymphoblastic leukemia patients
Heerema, Nyla AMaben, Kathleen DBernstein, JonathanBreitfeld, Philip PNeiman, Richard S and Vance, Gail H
Cancer Genetics and Cytogenetics, vol. 92, (no. 2), pp. 115, 1996. | Journal Article
1995
Cytogenetic and molecular analysis of a ring (21) in a patient with partial trisomy 21 and megakaryocytic leukemia
Palmer, CGBlouin, J-LBull, MJBreitfeld, P.Vance, Gail HVan Meter, T.Weaver, David DHeerema, NAColbern, SGKorenberg, J. RAntonarakis, SE and Chen, X.
American Journal of Medical Genetics Part A, vol. 57, (no. 4), pp. 527-536, 1995. | Journal Article
 
Testing for BRCA1 in Hereditary Breast Cancer
Vance, Gail H
JAMA, vol. 273, (no. 11), pp. 846, 1995-03-15. | Journal Article
1993
Cytogenetic findings of a child with transcobalamin II deficiency
Vance, Gail HMoncino, Mark and Heerema, Nyla A
American Journal of Medical Genetics, vol. 46, (no. 6), pp. 619, 1 July 1993. | Journal Article