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Results: 1-25 | 26-50 | 51-55
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LOSS OF 18Q PREDICTS POOR SURVIVAL OF PATIENTS WITH SQUAMOUS-CELL CARCINOMA OF THE HEAD AND NECK
Authors: PEARLSTEIN RP BENNINGER MS CAREY TE ZARBO RJ TORRES FX RYBICKI BA VANDYKE DL
Citation: Rp. Pearlstein et al., LOSS OF 18Q PREDICTS POOR SURVIVAL OF PATIENTS WITH SQUAMOUS-CELL CARCINOMA OF THE HEAD AND NECK, Genes, chromosomes & cancer, 21(4), 1998, pp. 333-339
PATERNAL UNIPARENTAL DISOMY 13 INVOLVING ISOCHROMOSOMES
Authors: BEREND SA MCCASKILL C CZARNECKI P FELDMAN GL VANDYKE DL SHAFFER LG
Citation: Sa. Berend et al., PATERNAL UNIPARENTAL DISOMY 13 INVOLVING ISOCHROMOSOMES, Cytogenetics and cell genetics, 82(1-2), 1998, pp. 140-141
BILATERAL PETERS ANOMALY IN AN INFANT WITH 49,XXXXY SYNDROME
Authors: MONAGHAN KG DENNEHY PJ VANDYKE DL WEISS L
Citation: Kg. Monaghan et al., BILATERAL PETERS ANOMALY IN AN INFANT WITH 49,XXXXY SYNDROME, Journal of pediatric ophthalmology and strabismus, 35(2), 1998, pp. 112-113
PRADER-WILLI-LIKE-SYNDROME IN A PATIENT WITH AN XQ23Q25 DUPLICATION
Authors: MONAGHAN KG VANDYKE DL FELDMAN GL
Citation: Kg. Monaghan et al., PRADER-WILLI-LIKE-SYNDROME IN A PATIENT WITH AN XQ23Q25 DUPLICATION, American journal of medical genetics, 80(3), 1998, pp. 227-231
DUPLICATION 6Q21Q23 IN 2 UNRELATED PATIENTS
Authors: PRATT VM ROBERSON JR WEISS L VANDYKE DL
Citation: Vm. Pratt et al., DUPLICATION 6Q21Q23 IN 2 UNRELATED PATIENTS, American journal of medical genetics, 80(2), 1998, pp. 112-114
7 NEW CASES OF CAYLER CARDIOFACIAL SYNDROME WITH CHROMOSOME 22Q11.2 DELETION, INCLUDING A FAMILIAL CASE
Authors: BAWLE EV CONARD J VANDYKE DL CZARNECKI P DRISCOLL DA
Citation: Ev. Bawle et al., 7 NEW CASES OF CAYLER CARDIOFACIAL SYNDROME WITH CHROMOSOME 22Q11.2 DELETION, INCLUDING A FAMILIAL CASE, American journal of medical genetics, 79(5), 1998, pp. 406-410
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 MOTHER WITH VCFS AND UNILATERAL DYSPLASTIC KIDNEY AND HER FETUS WITH MULTICYSTIC DYSPLASTIC KIDNEYS - ADDITIONAL EVIDENCE TO SUPPORT THE ASSOCIATION OF RENAL MALFORMATIONS AND VCFS
Authors: CZARNECKI PM VANDYKE DL FELDMAN GL
Citation: Pm. Czarnecki et al., A MOTHER WITH VCFS AND UNILATERAL DYSPLASTIC KIDNEY AND HER FETUS WITH MULTICYSTIC DYSPLASTIC KIDNEYS - ADDITIONAL EVIDENCE TO SUPPORT THE ASSOCIATION OF RENAL MALFORMATIONS AND VCFS, Journal of Medical Genetics, 35(4), 1998, pp. 348-348
GENETIC-ANALYSIS OF PRIMARY AND SECONDARY HEAD AND NECK TUMORS
Authors: CAREY TE WORSHAM MJ VANDYKE DL FRANK CJ JUNG KY PHAN BA
Citation: Te. Carey et al., GENETIC-ANALYSIS OF PRIMARY AND SECONDARY HEAD AND NECK TUMORS, British Journal of Cancer, 77, 1998, pp. 111-111
THE SPREADING OF X-INACTIVATION INTO AUTOSOMAL MATERIAL OF AN X-AUTOSOME TRANSLOCATION - EVIDENCE FOR A DIFFERENCE BETWEEN AUTOSOMAL AND X-CHROMOSOMAL DNA
Authors: WHITE WM WILLARD HF VANDYKE DL WOLFF DJ
Citation: Wm. White et al., THE SPREADING OF X-INACTIVATION INTO AUTOSOMAL MATERIAL OF AN X-AUTOSOME TRANSLOCATION - EVIDENCE FOR A DIFFERENCE BETWEEN AUTOSOMAL AND X-CHROMOSOMAL DNA, American journal of human genetics, 63(1), 1998, pp. 20-28
CHARACTERIZATION OF NEO-CENTROMERES IN MARKER CHROMOSOMES LACKING DETECTABLE ALPHA-SATELLITE DNA
Authors: DEPINET TW ZACKOWSKI JL EARNSHAW WC KAFFE S SEKHON GS STALLARD R SULLIVAN BA VANCE GH VANDYKE DL WILLARD HF ZINN AB SCHWARTZ S
Citation: Tw. Depinet et al., CHARACTERIZATION OF NEO-CENTROMERES IN MARKER CHROMOSOMES LACKING DETECTABLE ALPHA-SATELLITE DNA, Human molecular genetics, 6(8), 1997, pp. 1195-1204
FREQUENT LOSS OF HETEROZYGOSITY ON CHROMOSOME ARM 18Q IN SQUAMOUS-CELL CARCINOMAS - IDENTIFICATION OF 2 REGIONS OF LOSS - 18Q11.1-Q12.3 AND18Q21.1-Q23
Authors: JONES JW RAVAL JR BEALS TF WORSHAM MJ VANDYKE DL ESCLAMADO RM WOLF GT BRADFORD CR MILLER T CAREY TE
Citation: Jw. Jones et al., FREQUENT LOSS OF HETEROZYGOSITY ON CHROMOSOME ARM 18Q IN SQUAMOUS-CELL CARCINOMAS - IDENTIFICATION OF 2 REGIONS OF LOSS - 18Q11.1-Q12.3 AND18Q21.1-Q23, Archives of otolaryngology, head & neck surgery, 123(6), 1997, pp. 610-614
DELETIONS IN XQ26.3-Q27.3 INCLUDING FMR1 RESULT IN A SEVERE PHENOTYPEIN A MALE AND VARIABLE PHENOTYPES IN FEMALES DEPENDING UPON THE X-INACTIVATION PATTERN
Authors: WOLFF DJ GUSTASHAW KM ZURCHER V KO L WHITE W WEISS L VANDYKE DL SCHWARTZ S WILLARD HF
Citation: Dj. Wolff et al., DELETIONS IN XQ26.3-Q27.3 INCLUDING FMR1 RESULT IN A SEVERE PHENOTYPEIN A MALE AND VARIABLE PHENOTYPES IN FEMALES DEPENDING UPON THE X-INACTIVATION PATTERN, Human genetics, 100(2), 1997, pp. 256-262
RARE TRISOMY MOSAICISM DIAGNOSED IN AMNIOCYTES, INVOLVING AN AUTOSOMEOTHER THAN CHROMOSOME-13, CHROMOSOME-18, CHROMOSOME-20, AND CHROMOSOME-21 - KARYOTYPE PHENOTYPE CORRELATIONS/
Authors: HSU LYF YU MT NEU RL VANDYKE DL BENN PA BRADSHAW CL SHAFFER LG HIGGINS RR KHODR GS MORTON CC WANG HS BROTHMAN AR CHADWICK D DISTECHE CM JENKINS LS KALOUSEK DK PANTZAR TJ WYATT P
Citation: Lyf. Hsu et al., RARE TRISOMY MOSAICISM DIAGNOSED IN AMNIOCYTES, INVOLVING AN AUTOSOMEOTHER THAN CHROMOSOME-13, CHROMOSOME-18, CHROMOSOME-20, AND CHROMOSOME-21 - KARYOTYPE PHENOTYPE CORRELATIONS/, Prenatal diagnosis, 17(3), 1997, pp. 201-242
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
THE CYTO2000 COLLABORATIVE STUDY OF AMNIOTIC-FLUID CELL MOSAICISM - APARADIGM FOR INVESTIGATING THE SCIENCE AND PRACTICE OF CYTOGENETICS
Authors: ING PS VANDYKE DL CAUDILL SP REIDY JA CHEN ATL
Citation: Ps. Ing et al., THE CYTO2000 COLLABORATIVE STUDY OF AMNIOTIC-FLUID CELL MOSAICISM - APARADIGM FOR INVESTIGATING THE SCIENCE AND PRACTICE OF CYTOGENETICS, American journal of human genetics, 61(4), 1997, pp. 268-268
MOSAICISM FOR A BALANCED STRUCTURAL CHROMOSOMAL REARRANGEMENT
Authors: HEIL M EBRAHIM SAD VANDYKE DL MICALE MA KURCZYNSKI TW YARON Y EVANS MI
Citation: M. Heil et al., MOSAICISM FOR A BALANCED STRUCTURAL CHROMOSOMAL REARRANGEMENT, American journal of human genetics, 61(4), 1997, pp. 722-722
DUPLICATION 6Q21Q23 SYNDROME
Authors: PRATT VM ROBERSON JR WEISS L VANDYKE DL
Citation: Vm. Pratt et al., DUPLICATION 6Q21Q23 SYNDROME, American journal of human genetics, 61(4), 1997, pp. 784-784
SATELLITED CHROMOSOME-10 DETECTED PRENATALLY IN FETUS AND MOSAIC IN APARENT
Authors: OMALLEY DP DIEHN T BULLARD B NETZLOFF ML VANDYKE DL FELDMAN GL LEDBETTER D LESE C PRECHT K STORTO P
Citation: Dp. Omalley et al., SATELLITED CHROMOSOME-10 DETECTED PRENATALLY IN FETUS AND MOSAIC IN APARENT, American journal of human genetics, 61(4), 1997, pp. 913-913
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
IDENTIFYING GENETIC CHANGES ASSOCIATED WITH TUMOR PROGRESSION IN SQUAMOUS-CELL CARCINOMA
Authors: CAREY TE FRANK CJ RAVAL JR JONES JW MCCLATCHEY KD BEALS TF WORSHAM MJ VANDYKE DL
Citation: Te. Carey et al., IDENTIFYING GENETIC CHANGES ASSOCIATED WITH TUMOR PROGRESSION IN SQUAMOUS-CELL CARCINOMA, Acta oto-laryngologica, 1997, pp. 229-232
2 REGIONS OF HOMOZYGOSITY ON CHROMOSOME 3P IN SQUAMOUS-CELL CARCINOMAOF THE HEAD AND NECK COMPARISON WITH CYTOGENETIC ANALYSIS
Authors: BUCHHAGEN DL WORSHAM MJ VANDYKE DL CAREY TE
Citation: Dl. Buchhagen et al., 2 REGIONS OF HOMOZYGOSITY ON CHROMOSOME 3P IN SQUAMOUS-CELL CARCINOMAOF THE HEAD AND NECK COMPARISON WITH CYTOGENETIC ANALYSIS, Head & neck, 18(6), 1996, pp. 529-537
COMPARISON OF FREQUENCY OF LOH FOR BRCA1 IN AFRICAN-AMERICAN AND EUROPEAN-AMERICAN WOMEN WITH STAGE-III AND STAGE-IV BREAST-CANCER
Authors: WORSHAM MJ WOLMAN SR JOHNSON CC RAJU U BLOUNT A ABRAMS J NATHANSON SD ZARBO RJ MERAVJER SD VANDYKE DL FELDMAN GL
Citation: Mj. Worsham et al., COMPARISON OF FREQUENCY OF LOH FOR BRCA1 IN AFRICAN-AMERICAN AND EUROPEAN-AMERICAN WOMEN WITH STAGE-III AND STAGE-IV BREAST-CANCER, The FASEB journal, 10(6), 1996, pp. 2407-2407
LOSS OF 18Q AND HOMOZYGOSITY FOR THE DCC LOCUS - POSSIBLE MARKERS FORCLINICALLY AGGRESSIVE SQUAMOUS-CELL CARCINOMA
Authors: KELKER W VANDYKE DL WORSHAM MJ CHRISTOPHERSON PL JAMES CD CONLON MR CAREY TE
Citation: W. Kelker et al., LOSS OF 18Q AND HOMOZYGOSITY FOR THE DCC LOCUS - POSSIBLE MARKERS FORCLINICALLY AGGRESSIVE SQUAMOUS-CELL CARCINOMA, Anticancer research, 16(4C), 1996, pp. 2365-2372
INCIDENCE AND SIGNIFICANCE OF CHROMOSOME MOSAICISM INVOLVING AN AUTOSOMAL STRUCTURAL ABNORMALITY DIAGNOSED PRENATALLY THROUGH AMNIOCENTESIS- A COLLABORATIVE STUDY
Authors: HSU LYF YU MT RICHKIND KE VANDYKE DL CRANDALL BF SAXE DF KHODR GS MENNUTI M STETTEN G MILLER WA PRIEST JH
Citation: Lyf. Hsu et al., INCIDENCE AND SIGNIFICANCE OF CHROMOSOME MOSAICISM INVOLVING AN AUTOSOMAL STRUCTURAL ABNORMALITY DIAGNOSED PRENATALLY THROUGH AMNIOCENTESIS- A COLLABORATIVE STUDY, Prenatal diagnosis, 16(1), 1996, pp. 1-28
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