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Results: 1-25/28
Authors:
SCHNEIDER BF
LOVELL MA
GOLDEN WL
Citation: Bf. Schneider et al., CYTOGENETIC ABNORMALITIES IN PRIMARY BRONCHOPULMONARY LEIOMYOSARCOMA OF CHILDHOOD, Cancer genetics and cytogenetics, 105(2), 1998, pp. 145-151
Authors:
KELLY TE
FRANKO JB
ROGOL A
GOLDEN WL
Citation: Te. Kelly et al., DISCORDANT PHENOTYPES AND 45,X 46,X,IDIC(Y), Journal of Medical Genetics, 35(10), 1998, pp. 862-864
Authors:
VIDAEUS CM
VONKAPHERR C
GOLDEN WL
EDDY RL
SHOWS TB
HERR JC
Citation: Cm. Vidaeus et al., HUMAN FERTILIN-BETA - IDENTIFICATION, CHARACTERIZATION, AND CHROMOSOMAL MAPPING OF AN ADAM GENE FAMILY MEMBER, Molecular reproduction and development, 46(3), 1997, pp. 363-369
Authors:
IEZZONI JC
VONKAPHERR C
GOLDEN WL
GAFFEY MJ
Citation: Jc. Iezzoni et al., GONADOBLASTOMAS IN 45,X 46,XY MOSAICISM - ANALYSIS OF Y-CHROMOSOME DISTRIBUTION BY FLUORESCENCE IN-SITU HYBRIDIZATION/, American journal of clinical pathology, 108(2), 1997, pp. 197-201
Authors:
GOLDEN WL
LOVELL MA
SUDDUTH KW
SCHNEIDER BF
Citation: Wl. Golden et al., CYTOGENETIC ABNORMALITIES IN A PRIMARY BRONCHOPULMONARY LEIOMYOSARCOMA OF CHILDHOOD, Cytogenetics and cell genetics, 74(4), 1996, pp. 308-308
Authors:
FRYBURG JS
LIN KY
GOLDEN WL
Citation: Js. Fryburg et al., CHROMOSOME 22Q11.2 DELETION IN A BOY WITH OPITZ (G BBB) SYNDROME/, American journal of medical genetics, 62(3), 1996, pp. 274-275
Authors:
SHASHI V
GOLDEN WL
VONKAPHERR C
WILSON WG
Citation: V. Shashi et al., CONSTELLATION OF CONGENITAL-ABNORMALITIES IN AN INFANT - A NEW SYNDROME OR TISSUE-SPECIFIC MOSAICISM FOR TRISOMY-18, American journal of medical genetics, 62(1), 1996, pp. 38-41
Authors:
SHASHI V
GOLDEN WL
ALLINSON PS
BLANTON SH
VONKAPHERR C
KELLY TE
Citation: V. Shashi et al., MOLECULAR ANALYSIS OF RECOMBINATION IN A FAMILY WITH DUCHENNE MUSCULAR-DYSTROPHY AND A LARGE PERICENTRIC X-CHROMOSOME INVERSION, American journal of human genetics, 58(6), 1996, pp. 1231-1238
Authors:
VONKAPHERR C
MISCHEN B
WILSON WG
GOLDEN WL
Citation: C. Vonkapherr et al., MOSAICISM FOR A MARKER FORMED BY UNEQUAL CROSSING-OVER BETWEEN HOMOLOGOUS 13S, RESULTING IN A SUPERNUMERARY DEL(13)(Q14-]QTER), Cytogenetics and cell genetics, 71(4), 1995, pp. 395-395
Authors:
SCHNEIDER BF
VANDENBERG SR
SUDDUTH KW
VONKAPHERR C
SHASHI V
GOLDEN WL
Citation: Bf. Schneider et al., STRUCTURAL ABNORMALITIES OF CHROMOSOME-14 IN MENINGIOMAS - EVIDENCE FOR A PROGRESSION GENE, Cytogenetics and cell genetics, 69(1-2), 1995, pp. 124-124
Authors:
SCHNEIDER BF
SHASHI V
VONKAPHERR C
GOLDEN WL
Citation: Bf. Schneider et al., LOSS OF CHROMOSOME-22 AND CHROMOSOME-14 IN THE MALIGNANT PROGRESSION OF MENINGIOMAS - A COMPARATIVE-STUDY OF FLUORESCENCE IN-SITU HYBRIDIZATION (FISH) AND STANDARD CYTOGENETIC ANALYSIS, Cancer genetics and cytogenetics, 85(2), 1995, pp. 101-104
Authors:
LEZZONI JC
VONKAPHERR C
GOLDEN WL
GAFFEY MJ
Citation: Jc. Lezzoni et al., Y-CHROMOSOME DISTRIBUTION IN BILATERAL GONADOBLASTOMAS (GB) IN A PATIENT WITH A 45,X 46,XY MOSAICISM - ANALYSIS WITH FLUORESCENCE IN-SITU HYBRIDIZATION (FISH)/, Laboratory investigation, 72(1), 1995, pp. 91-91
Authors:
SCHNATTERLY PT
FRYBURG J
GOLDEN WL
KELLY TE
Citation: Pt. Schnatterly et al., A BALANCED CHROMOSOME-TRANSLOCATION (1-13)(Q42-Q22) RESULTING IN 3 LIVE-BORN CHILDREN WITH 3 DIFFERENT UNBALANCED CHROMOSOME COMPLEMENTS - BOTH ADJACENT 1 MEIOTIC SEGREGATIONS AND 3 1 TERTIARY TRISOMY/, American journal of human genetics, 57(4), 1995, pp. 704-704
Authors:
MCKINNEY CD
GOLDEN WL
GEMMA NW
SWERDLOW SH
WILLIAMS ME
Citation: Cd. Mckinney et al., RARA AND PML GENE REARRANGEMENTS IN ACUTE PROMYELOCYTIC LEUKEMIA WITHCOMPLEX TRANSLOCATIONS AND ATYPICAL FEATURES, Genes, chromosomes & cancer, 9(1), 1994, pp. 49-56
Authors:
SHASHI V
LOVELL MA
VONKAPHERR C
WALDRON P
GOLDEN WL
Citation: V. Shashi et al., MALIGNANT RHABDOID TUMOR OF THE KIDNEY - INVOLVEMENT OF CHROMOSOME-22, Genes, chromosomes & cancer, 10(1), 1994, pp. 49-54
Authors:
GAYLINN BD
VONKAPHERR C
GOLDEN WL
THORNER MO
Citation: Bd. Gaylinn et al., ASSIGNMENT OF THE HUMAN GROWTH HORMONE-RELEASING HORMONE-RECEPTOR GENE (GHRHR) TO 7P14 BY IN-SITU HYBRIDIZATION, Genomics, 19(1), 1994, pp. 193-195
Authors:
SHASHI V
GOLDEN WL
FRYBURG JS
Citation: V. Shashi et al., CHOANAL ATRESIA IN A PATIENT WITH THE DELETION (9P) SYNDROME, American journal of medical genetics, 49(1), 1994, pp. 88-90
Authors:
SHASHI V
GOLDEN WL
VONKAPHERR C
ANDERSEN WA
GAFFEY MJ
Citation: V. Shashi et al., INTERPHASE FLUORESCENCE IN-SITU HYBRIDIZATION FOR TRISOMY-12 ON ARCHIVAL OVARIAN SEX CORD-STROMAL TUMORS, Gynecologic oncology, 55(3), 1994, pp. 349-354
Authors:
SHASHI V
ALLINSON PS
GOLDEN WL
KELLY TE
Citation: V. Shashi et al., DECREASED RECOMBINATION IN OOGENESIS IN A FAMILY WITH A LARGE PERICENTRIC X-CHROMOSOME INVERSION, Pediatric research, 35(4), 1994, pp. 10000154-10000154
Authors:
MCCLELLAN MW
GOLDEN WL
WILSON WG
Citation: Mw. Mcclellan et al., MARFAN AND CRI DU CHAT SYNDROMES IN AN 18-MONTH-OLD CHILD - EVIDENCE OF PHENOTYPE INTERACTION, Clinical genetics, 46(4), 1994, pp. 319-321
Authors:
GOLDEN WL
VONKAPHERR C
KURTH B
WRIGHT RM
FLICKINGER CJ
EDDY R
SHOWS T
HERR JC
Citation: Wl. Golden et al., REFINEMENT OF THE LOCALIZATION OF THE GENE FOR HUMAN INTRAACROSOMAL PROTEIN SP-10 (ACRV1) TO THE JUNCTION OF BANDS Q23 -] Q24 OF CHROMOSOME-11 BY NONISOTOPIC IN-SITU HYBRIDIZATION, Genomics, 18(2), 1993, pp. 446-449
Authors:
SHASHI V
LOVELL MA
GOLDEN WL
Citation: V. Shashi et al., MALIGNANT RHABDOID TUMOR OF THE KIDNEY - INVOLVEMENT OF CHROMOSOME-22, Cytogenetics and cell genetics, 63(4), 1993, pp. 257-257
Authors:
DONEY MK
HOUSEAL TW
SOUKUP SW
RUTTER JL
GUSELLA JF
SCHNEIDER BF
GOLDEN WL
MENON AG
Citation: Mk. Doney et al., IDENTIFICATION OF A PUTATIVE TUMOR-SUPPRESSOR LOCUS IN 14Q24-32 THAT IS INVOLVED IN FORMATION AND PROGRESSION OF MENINGIOMAS, American journal of human genetics, 53(3), 1993, pp. 293-293
Authors:
GOLDEN WL
SHASHI V
VONKAPHERR C
SUDDUTH KW
SCHNEIDER BF
Citation: Wl. Golden et al., COMPARATIVE FLUORESCENT IN-SITU HYBRIDIZATION AND STANDARD CYTOGENETIC ANALYSIS IN MENINGIOMAS, American journal of human genetics, 53(3), 1993, pp. 302-302
Authors:
SHASHI V
GOLDEN WL
VONKAPHERR C
GAFFEY MJ
Citation: V. Shashi et al., INTERPHASE CYTOGENETIC ANALYSIS FOR TRISOMY-12 IN OVARIAN SEX CORD-STROMAL TUMORS, American journal of human genetics, 53(3), 1993, pp. 364-364