98 Publications (Page 4 of 4)
2001
Improvements in cytogenetic slide preparation: Controlled chromosome spreading, chemical aging and gradual denaturingHenegariu, Octavian⋅Heerema, Nyla A⋅Lowe Wright, Lisa⋅Bray‐Ward, Patricia⋅Ward, David C and Vance, Gail HCytometry, vol. 43, (no. 2), pp. 109, 1 February 2001.
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Validation of Scales to Measure Benefits of and Barriers to Colorectal Cancer ScreeningRawl, Susan M⋅Rawl, Susan⋅Champion, Victoria L⋅Champion, Victoria⋅Menon, Usha⋅Menon, Usha⋅Loehrer, Patrick J⋅Loehrer, Patrick J⋅Vance, Gail H⋅Vance, Gail H⋅Skinner, Celette S and Skinner, Celette SuggJournal of Psychosocial Oncology, vol. 19, (no. 3-4), pp. 63, 12/3/2001.
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Detection of Monosomy 7 in Bone Marrow by Fluorescence In Situ HybridizationThurston, Virginia C⋅Ceperich, Tina M⋅Vance, Gail H and Heerema, Nyla ACancer Genetics and Cytogenetics, vol. 109, (no. 2), pp. 160, 1999-03-00.
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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 C⋅Ceperich, T M⋅Vance, Gail H and Heerema, N ACancer genetics and cytogenetics, vol. 109, (no. 2), pp. 154-60, 1999/Mar.
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Detection of Mosaicism in amniotic fluid cultures: A CYT02000 collaborative studyIng, Paul S⋅Van Dyke, Daniel L⋅Caudill, Samuel P⋅Reidy, John A⋅Bice, Gillian⋅Bieber, Frederick R⋅Buchanan, Phillip D⋅Carroll, Andrew J⋅Cheung, Sau W⋅Dewald, Gordon⋅Donahue, Roger P⋅Gardner, H Allen⋅Higgins, James⋅Hsu, Lillian Ye⋅Jamehdor, Mehdi⋅Keitges, Elisabeth A⋅Laundon, Caroline H⋅Luthardt, Frederick W⋅Mascarello, James⋅May, Kristin M⋅Meck, Jeanne M⋅Morton, Cynthia⋅Patil, Shiva⋅Peakman, David⋅Pettenati, Mark J⋅Rao, Nagesh⋅Sanger, Warren G⋅Saxe, Deborah F⋅Schwartz, Stuart⋅Sekhon, Gurbax S⋅Vance, Gail H⋅Wyandt, Herman E⋅Yu, Cheng W⋅Zenger-Hain, Julie and L. Chen, Andrew TGenetics in Medicine, vol. 1, (no. 3), pp. 97, 1999-04-00.
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Detection of mosaicism in amniotic fluid cultures: a CYTO2000 collaborative study.Ing, P S⋅Van Dyke, Daniel L⋅Caudill, S P⋅Reidy, J A⋅Bice, G⋅Bieber, Frederick R⋅Buchanan, P D⋅Carroll, A J⋅Cheung, Steven W⋅Dewald, Gordon W⋅Donahue, R P⋅Gardner, H A⋅Higgins, J⋅Hsu, L Y⋅Jamehdor, M⋅Keitges, E A⋅Laundon, C H⋅Luthardt, F W⋅Mascarello, J⋅May, K M⋅Meck, J M⋅Morton, Cynthia C⋅Patil, S⋅Peakman, D⋅Pettenati, M J⋅Rao, N⋅Sanger, W G⋅Saxe, D F⋅Schwartz, S⋅Sekhon, G S⋅Vance, Gail H⋅Wyandt, H E⋅Yu, Cheng W⋅Zenger-Hain, J and Chen, A TGenetics in medicine : official journal of the American College of Medical Genetics, vol. 1, (no. 3), pp. 94-7, 1999 Mar-Apr.
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1998
A multicenter investigation with interphase fluorescence in situ hybridization using X‐ and Y‐chromosome probesDewald, Gordon W⋅Dewald, Gordon⋅Stallard, Richard⋅Stallard, R⋅Al Saadi, A⋅Saadi, A. Al⋅Arnold, Susan⋅Arnold, S⋅Bader, Patricia I⋅Bader, P I⋅Blough, R⋅Blough, Ruthann⋅Chen, K⋅Chen, Kathy⋅Elejalde, B. Rafael⋅Elejalde, B R⋅Harris, Catherine J⋅Harris, C J⋅Higgins, R R⋅Higgins, Rodney R⋅Hoeltge, G A⋅Hoeltge, Gerald A⋅Hsu, Wei‐Tong⋅Hsu, W T⋅Kubic, Virginia⋅Kubic, V⋅McCorquodale, D. James⋅McCorquodale, D J⋅Micale, Mark A⋅Micale, M A⋅Moore, J W⋅Moore, J.W⋅Phillips, R M⋅Phillips, Rosalie M⋅Scheib-Wixted, S⋅Scheib‐Wixted, Susan⋅Schwartz, S⋅Schwartz, Stuart⋅Siembieda, Steven⋅Siembieda, S⋅Strole, Kathy⋅Strole, K⋅VanTuinen, Peter⋅VanTuinen, P⋅Vance, G H⋅Vance, Gail H⋅Wiktor, A⋅Wiktor, Ann⋅Zinsmeister, A⋅Wise, Laura⋅Yung, Jar‐Fee⋅Zenger‐Hain, Julie and Zinsmeister, AlanAmerican Journal of Medical Genetics, vol. 76, (no. 4), pp. 326, 1 April 1998.
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Characterization of Multiple 12p Rearrangements in Testicular Germ Cell Tumor Cell Line 833K and Its Subclone 64CP by Chromosome MicrodissectionBlough, Ruthann I⋅Vance, Gail H⋅Henegariu, Octavian⋅Smolarek, Teresa A⋅Sledge, George W and Heerema, Nyla ACancer Genetics and Cytogenetics, vol. 106, (no. 1), pp. 29, 1998.
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Cytogenetics: a short review and update.Vance, Gail HCancer Investigation, vol. 16, (no. 1), pp. 40-4, 1998.
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Molecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7q.Vance, Gail H⋅Nickerson, C⋅Sarnat, L⋅Zhang, A⋅Henegariu, O⋅Morichon-Delvallez, N⋅Butler, Merlin G and Palmer, C GAmerican journal of medical genetics, vol. 76, (no. 1), pp. 51-7, 1998/Feb/26.
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Partners with reciprocal translocations: genetic counseling for the ‘double translocation’Cook, L⋅Cook, Lola⋅Hartsfield, James K⋅Hartsfield, James K⋅Vance, G H and Vance, Gail HClinical Genetics, vol. 53, (no. 5), pp. 407, May 1998.
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Triple-color FISH analysis of 12p amplification in testicular germ-cell tumors using 12p band-specific painting probesHenegariu, O⋅Vance, Gail H⋅Heiber, Devan⋅Pera, Martin and Heerema, Nyla AJournal of Molecular Medicine, vol. 76, (no. 9), pp. 655, 19980700.
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Variable phenotype of familial adenomatous polyposis in pedigrees with 3' mutation in the APC gene.Brensinger, J D⋅Laken, S J⋅Luce, M C⋅Powell, Steven M⋅Vance, Gail H⋅Ahnen, D J⋅Petersen, G M⋅Hamilton, Stanley R and Giardiello, Francis MGut, vol. 43, (no. 4), pp. 548-52, 1998/Oct.
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1997
A case with mosaic di-, tetra-, and octacentric ring Y chromosomes.Henegariu, O⋅Pescovitz, O H⋅Vance, Gail H⋅Verbrugge, J and Heerema, N AAmerican journal of medical genetics, vol. 71, (no. 4), pp. 426-9, 1997/Sep/5.
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An apparently acentric marker chromosome originating from 9p with a functional centromere without detectable alpha and beta satellite sequences.Vance, Gail H⋅Curtis, C A⋅Heerema, N A⋅Schwartz, S and Palmer, C GAmerican journal of medical genetics, vol. 71, (no. 4), pp. 436-42, 1997/Sep/5.
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Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNADepinet, TW⋅Zackowski, JL⋅Earnshaw, William C⋅Kaffe, S.⋅Sekhon, GS⋅Stallard, R.⋅Sullivan, Beth A⋅Vance, Gail H⋅Van Dyke, Daniel L⋅Willard, Huntington F⋅Zinn, AB and Schwartz, S.Human Molecular Genetics, vol. 6, (no. 8), pp. 1195-1204, 1997.
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Mild "duplication 6q syndrome": a case with partial trisomy (6)(q23.3q25.3).Henegariu, O⋅Heerema, N A and Vance, Gail HAmerican journal of medical genetics, vol. 68, (no. 4), pp. 450-4, 1997/Feb/11.
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Urorectal septum malformation sequence: Report of thirteen additional cases and review of the literatureWheeler, Patricia G⋅Wheeler, Patricia G⋅Weaver, David D⋅Weaver, David D⋅Obeime, Mercy O⋅Obeime, Mercy O⋅Vance, Gail H⋅Vance, Gail H⋅Bull, Marilyn J⋅Bull, Marilyn J⋅Escobar, Luis F and Escobar, Luis FAmerican Journal of Medical Genetics, vol. 73, (no. 4), pp. 462, 31 December 1997.
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1996
Dicentric (9;20)(p11;q11) identified by fluorescence in situ hybridization in four pediatric acute lymphoblastic leukemia patientsHeerema, Nyla A⋅Maben, Kathleen D⋅Bernstein, Jonathan⋅Breitfeld, Philip P⋅Neiman, Richard S and Vance, Gail HCancer Genetics and Cytogenetics, vol. 92, (no. 2), pp. 115, 1996.
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1995
Cytogenetic and molecular analysis of a ring (21) in a patient with partial trisomy 21 and megakaryocytic leukemiaPalmer, CG⋅Blouin, J-L⋅Bull, MJ⋅Breitfeld, P.⋅Vance, Gail H⋅Van Meter, T.⋅Weaver, David D⋅Heerema, NA⋅Colbern, SG⋅Korenberg, J. R⋅Antonarakis, SE and Chen, X.American Journal of Medical Genetics Part A, vol. 57, (no. 4), pp. 527-536, 1995.
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Testing for BRCA1 in Hereditary Breast CancerVance, Gail HJAMA, vol. 273, (no. 11), pp. 846, 1995-03-15.
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1993
Cytogenetic findings of a child with transcobalamin II deficiencyVance, Gail H⋅Moncino, Mark and Heerema, Nyla AAmerican Journal of Medical Genetics, vol. 46, (no. 6), pp. 619, 1 July 1993.
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