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Results: 76-91/91
A MICROSATELLITE-BASED MULTIPOINT INDEX MAP OF HUMAN-CHROMOSOME-22
Authors: BUETOW KH DUGGAN D YANG BS LUDWIGSEN S PUCK J PORTER J BUDARF M SPIELMAN R EMANUEL BS
Citation: Kh. Buetow et al., A MICROSATELLITE-BASED MULTIPOINT INDEX MAP OF HUMAN-CHROMOSOME-22, Genomics, 18(2), 1993, pp. 329-339
A PANEL OF SEQUENCE-TAGGED SITES FOR CHROMOSOME BAND-11Q23
Authors: TUNNACLIFFE A PERRY H RADICE P BUDARF ML EMANUEL BS
Citation: A. Tunnacliffe et al., A PANEL OF SEQUENCE-TAGGED SITES FOR CHROMOSOME BAND-11Q23, Genomics, 17(3), 1993, pp. 744-747
PHYSICAL MAPPING STUDIES OF THE T(2,13) TRANSLOCATION BREAKPOINT IN ALVEOLAR RHABDOMYOSARCOMA
Authors: BARR FG EMANUEL BS
Citation: Fg. Barr et Bs. Emanuel, PHYSICAL MAPPING STUDIES OF THE T(2,13) TRANSLOCATION BREAKPOINT IN ALVEOLAR RHABDOMYOSARCOMA, Cytogenetics and cell genetics, 64(2), 1993, pp. 87-87
REPORT OF THE 3RD INTERNATIONAL WORKSHOP ON HUMAN CHROMOSOME-22 MAPPING
Authors: EMANUEL BS BUETOW K NUSSBAUM R SCAMBLER P LIPINSKI M OVERTON GC
Citation: Bs. Emanuel et al., REPORT OF THE 3RD INTERNATIONAL WORKSHOP ON HUMAN CHROMOSOME-22 MAPPING, Cytogenetics and cell genetics, 63(4), 1993, pp. 206-211
FLUORESCENCE IN-SITU HYBRIDIZATION STUDY USING PROBES FROM DIGEORGE-SYNDROME CRITICAL REGION ON PATIENTS WITH SUSPECTED SUBMICROSCOPIC DELETION ON CHROMOSOME-22
Authors: SELLINGER BT TATSUMURA YO GOLDMUNTZ E DRISCOLL DA EMANUEL BS BUDARF ML
Citation: Bt. Sellinger et al., FLUORESCENCE IN-SITU HYBRIDIZATION STUDY USING PROBES FROM DIGEORGE-SYNDROME CRITICAL REGION ON PATIENTS WITH SUSPECTED SUBMICROSCOPIC DELETION ON CHROMOSOME-22, Cytogenetics and cell genetics, 63(4), 1993, pp. 252-253
DIGEORGE ANOMALY WITH RENAL AGENESIS IN INFANTS OF MOTHERS WITH DIABETES
Authors: WILSON TA BLETHEN SL VALLONE A ALENICK DS NOLAN P KATZ A AMORILLO TP GOLDMUNTZ E EMANUEL BS DRISCOLL DA
Citation: Ta. Wilson et al., DIGEORGE ANOMALY WITH RENAL AGENESIS IN INFANTS OF MOTHERS WITH DIABETES, American journal of medical genetics, 47(7), 1993, pp. 1078-1082
MICRODELETIONS OF CHROMOSOMAL REGION 22Q11 IN PATIENTS WITH CONGENITAL CONOTRUNCAL CARDIAC DEFECTS
Authors: GOLDMUNTZ E DRISCOLL D BUDARF ML ZACKAI EH MCDONALDMCGINN DM BIEGEL JA EMANUEL BS
Citation: E. Goldmuntz et al., MICRODELETIONS OF CHROMOSOMAL REGION 22Q11 IN PATIENTS WITH CONGENITAL CONOTRUNCAL CARDIAC DEFECTS, Journal of Medical Genetics, 30(10), 1993, pp. 807-812
PREVALENCE OF 22Q11 MICRODELETIONS IN DIGEORGE AND VELOCARDIOFACIAL SYNDROMES - IMPLICATIONS FOR GENETIC-COUNSELING AND PRENATAL-DIAGNOSIS
Authors: DRISCOLL DA SALVIN J SELLINGER B BUDARF ML MCDONALDMCGINN DM ZACKAI EH EMANUEL BS
Citation: Da. Driscoll et al., PREVALENCE OF 22Q11 MICRODELETIONS IN DIGEORGE AND VELOCARDIOFACIAL SYNDROMES - IMPLICATIONS FOR GENETIC-COUNSELING AND PRENATAL-DIAGNOSIS, Journal of Medical Genetics, 30(10), 1993, pp. 813-817
THE MURINE HOMOLOG OF A UNIQUE GENE IN THE DIGEORGE CRITICAL REGION OF CHROMOSOME-22Q11 IS EXPRESSED DURING PHARYNGEAL ARCH DEVELOPMENT IN THE MOUSE EMBRYO
Authors: BALDWIN HS SHEN HM MICKANIN CS BUDARF M DRISCOLL D EMANUEL BS BUCK CA
Citation: Hs. Baldwin et al., THE MURINE HOMOLOG OF A UNIQUE GENE IN THE DIGEORGE CRITICAL REGION OF CHROMOSOME-22Q11 IS EXPRESSED DURING PHARYNGEAL ARCH DEVELOPMENT IN THE MOUSE EMBRYO, Circulation, 88(4), 1993, pp. 129-129
DIAGNOSIS OF CHROMOSOME-22 MICRODELETIONS IN PATIENTS WITH CONOTRUNCAL DEFECTS
Authors: GOLDMUNTZ E DRISCOLL D EMANUEL BS
Citation: E. Goldmuntz et al., DIAGNOSIS OF CHROMOSOME-22 MICRODELETIONS IN PATIENTS WITH CONOTRUNCAL DEFECTS, Circulation, 88(4), 1993, pp. 289-289
ISOLATION OF POLY-TG MARKERS IN THE DIGEORGE CRITICAL REGION (DGCR)
Authors: GORMAN CN BUETOW KH DUGAN D BUDARF ML EMANUEL BS DRISCOLL DA
Citation: Cn. Gorman et al., ISOLATION OF POLY-TG MARKERS IN THE DIGEORGE CRITICAL REGION (DGCR), American journal of human genetics, 53(3), 1993, pp. 184-184
CLINICAL AND CYTOGENETIC VARIABILITY IN TRISOMY-8 MOSAICISM
Authors: MCDONALDMCGINN DM GRACE K SPINNER NB EMANUEL BS ZACKAI EH
Citation: Dm. Mcdonaldmcginn et al., CLINICAL AND CYTOGENETIC VARIABILITY IN TRISOMY-8 MOSAICISM, American journal of human genetics, 53(3), 1993, pp. 222-222
REGION-SPECIFIC COSMID LIBRARY FROM THE FLOW-SORTED MARKER CHROMOSOMES OF CAT EYE SYNDROME
Authors: MINOSHIMA S KUDOH J WANG Y SHI J SAKAI K EMANUEL BS SHIMIZU N
Citation: S. Minoshima et al., REGION-SPECIFIC COSMID LIBRARY FROM THE FLOW-SORTED MARKER CHROMOSOMES OF CAT EYE SYNDROME, American journal of human genetics, 53(3), 1993, pp. 1330-1330
TOWARDS A YEAST ARTIFICIAL CHROMOSOME CONTIG OF HUMAN CHROMOSOME-22
Authors: NIEUWENHUIJSEN BW BUDARI ML CAMPBELL K COLLINS J DESJARDINS P VALMIKI VH WILLIAMS SR NUSSBAUM RL SEARIS DB OVERTON GC EMANUEL BS FISCHBECK KH
Citation: Bw. Nieuwenhuijsen et al., TOWARDS A YEAST ARTIFICIAL CHROMOSOME CONTIG OF HUMAN CHROMOSOME-22, American journal of human genetics, 53(3), 1993, pp. 1339-1339
PRENATAL-DIAGNOSIS OF CAT EYE SYNDROME BY FLUORESCENCE IN-SITU HYBRIDIZATION (FISH)
Authors: DRISCOLL DA SELLINGER B BUDARF ML EMANUEL BS MILLER RC DONNENFELD AE REESER SL
Citation: Da. Driscoll et al., PRENATAL-DIAGNOSIS OF CAT EYE SYNDROME BY FLUORESCENCE IN-SITU HYBRIDIZATION (FISH), American journal of human genetics, 53(3), 1993, pp. 1401-1401
VELO-CARDIO-FACIAL SYNDROME - INTRAFAMILIAL VARIABILITY OF THE PHENOTYPE
Authors: MCLEAN SD SAAL HM SPINNER NB EMANUEL BS DRISCOLL DA
Citation: Sd. Mclean et al., VELO-CARDIO-FACIAL SYNDROME - INTRAFAMILIAL VARIABILITY OF THE PHENOTYPE, American journal of diseases of children [1960], 147(11), 1993, pp. 1212-1216
Risultati: 1-25 | 26-50 | 51-75 | 76-91 |