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Results: 1-20 |
Results: 20
MOLECULAR CYTOGENETIC EVIDENCE FOR A COMMON BREAKPOINT IN THE LARGESTINVERTED DUPLICATIONS OF CHROMOSOME-15
Authors: WANDSTRAT AE LEANACOX J JENKINS L SCHWARTZ S
Citation: Ae. Wandstrat et al., MOLECULAR CYTOGENETIC EVIDENCE FOR A COMMON BREAKPOINT IN THE LARGESTINVERTED DUPLICATIONS OF CHROMOSOME-15, American journal of human genetics, 62(4), 1998, pp. 925-936
CONSTRUCTION AND SCREENING OF A COSMID LIBRARY GENERATED FROM A SOMATIC-CELL HYBRID BEARING HUMAN-CHROMOSOME-15
Authors: MCDANIEL LD ZHANG BQ KUBICZEK E RITTER M HUANG J BERARD C LEANACOX J SCHWARTZ S SCHULTZ RA
Citation: Ld. Mcdaniel et al., CONSTRUCTION AND SCREENING OF A COSMID LIBRARY GENERATED FROM A SOMATIC-CELL HYBRID BEARING HUMAN-CHROMOSOME-15, Genomics, 40(1), 1997, pp. 63-72
WHATS IN A NAME - THE 22Q11.2 DELETION - REPLY
Authors: WULFSBERG EA LEANACOX J NERI G
Citation: Ea. Wulfsberg et al., WHATS IN A NAME - THE 22Q11.2 DELETION - REPLY, American journal of medical genetics, 72(2), 1997, pp. 248-249
SEX-CHROMOSOME MARKERS - CHARACTERIZATION USING FLUORESCENCE IN-SITU HYBRIDIZATION AND REVIEW OF THE LITERATURE
Authors: SCHWARTZ S DEPINET TW LEANACOX J ISADA NB KARSON EM PARK VM PASZTOR LM SHEPPARD LC STALLARD R WOLFF DJ ZINN AB ZURCHER VL ZACKOWSKI JL
Citation: S. Schwartz et al., SEX-CHROMOSOME MARKERS - CHARACTERIZATION USING FLUORESCENCE IN-SITU HYBRIDIZATION AND REVIEW OF THE LITERATURE, American journal of medical genetics, 71(1), 1997, pp. 1-7
CHROMOSOME-7Q DUPLICATIONS - MOLECULAR CYTOGENETIC ANALYSIS AND CORRELATION WITH PHENOTYPE IN 2 CASES
Authors: STROVEL JW LEANACOX J STAMBERG J
Citation: Jw. Strovel et al., CHROMOSOME-7Q DUPLICATIONS - MOLECULAR CYTOGENETIC ANALYSIS AND CORRELATION WITH PHENOTYPE IN 2 CASES, Cytogenetics and cell genetics, 74(4), 1996, pp. 311-312
FAMILIAL DIGEORGE VELOCARDIOFACIAL SYNDROME WITH DELETIONS OF CHROMOSOME AREA 22Q11.2 - REPORT OF 5 FAMILIES WITH A REVIEW OF THE LITERATURE/
Authors: LEANACOX J PANGKANON S EANET KR CURTIN MS WULFSBERG EA
Citation: J. Leanacox et al., FAMILIAL DIGEORGE VELOCARDIOFACIAL SYNDROME WITH DELETIONS OF CHROMOSOME AREA 22Q11.2 - REPORT OF 5 FAMILIES WITH A REVIEW OF THE LITERATURE/, American journal of medical genetics, 65(4), 1996, pp. 309-316
WHATS IN A NAME - CHROMOSOME 22Q ABNORMALITIES AND THE DIGEORGE, VELOCARDIOFACIAL, AND CONOTRUNCAL ANOMALIES FACE SYNDROMES
Authors: WULFSBERG EA LEANACOX J NERI G
Citation: Ea. Wulfsberg et al., WHATS IN A NAME - CHROMOSOME 22Q ABNORMALITIES AND THE DIGEORGE, VELOCARDIOFACIAL, AND CONOTRUNCAL ANOMALIES FACE SYNDROMES, American journal of medical genetics, 65(4), 1996, pp. 317-319
EVIDENCE FOR STRUCTURAL HETEROGENEITY FROM MOLECULAR CYTOGENETIC ANALYSIS OF DICENTRIC ROBERTSONIAN TRANSLOCATIONS
Authors: SULLIVAN BA JENKINS LS KARSON EM LEANACOX J SCHWARTZ S
Citation: Ba. Sullivan et al., EVIDENCE FOR STRUCTURAL HETEROGENEITY FROM MOLECULAR CYTOGENETIC ANALYSIS OF DICENTRIC ROBERTSONIAN TRANSLOCATIONS, American journal of human genetics, 59(1), 1996, pp. 167-175
APPLICATION OF FISH TO COMPLEX CHROMOSOMAL REARRANGEMENTS ASSOCIATED WITH CHRONIC MYELOGENOUS LEUKEMIA
Authors: SULLIVAN BA SCHIFFER CA PATIL SR HULSEBERG D LEANACOX J SCHWARTZ S
Citation: Ba. Sullivan et al., APPLICATION OF FISH TO COMPLEX CHROMOSOMAL REARRANGEMENTS ASSOCIATED WITH CHRONIC MYELOGENOUS LEUKEMIA, Cancer genetics and cytogenetics, 82(2), 1995, pp. 93-99
IDENTIFICATION, DELINEATION AND PARENTAL ORIGIN OF UNBALANCED DE-NOVOREARRANGEMENTS WITH HIGH-RESOLUTION CHROMOSOMES, FISH AND MICROSATELLITE MARKERS - EXPERIENCE WITH 65 CASES
Authors: SCHWARTZ S BECKER LA CONROY JM DEPINET TW LEANACOX J MYERS EL WOLFF D
Citation: S. Schwartz et al., IDENTIFICATION, DELINEATION AND PARENTAL ORIGIN OF UNBALANCED DE-NOVOREARRANGEMENTS WITH HIGH-RESOLUTION CHROMOSOMES, FISH AND MICROSATELLITE MARKERS - EXPERIENCE WITH 65 CASES, American journal of human genetics, 57(4), 1995, pp. 82-82
MOLECULAR CHARACTERIZATION OF INVERTED DUPLICATIONS OF CHROMOSOME-15 - INSIGHT INTO MECHANISM OF FORMATION
Authors: WANDSTRAT AE LEANACOX J SCHWARTZ S
Citation: Ae. Wandstrat et al., MOLECULAR CHARACTERIZATION OF INVERTED DUPLICATIONS OF CHROMOSOME-15 - INSIGHT INTO MECHANISM OF FORMATION, American journal of human genetics, 57(4), 1995, pp. 168-168
PHENOTYPIC VARIABILITY ASSOCIATED WITH DEL(22)(Q11.2) - A REPORT OF 5FAMILIAL CASES
Authors: LEANACOX J PANGKANON S SUPOVITZ KR CURTIN MS WULFSBERG EA
Citation: J. Leanacox et al., PHENOTYPIC VARIABILITY ASSOCIATED WITH DEL(22)(Q11.2) - A REPORT OF 5FAMILIAL CASES, American journal of human genetics, 57(4), 1995, pp. 523-523
MOLECULAR CYTOGENETIC ANALYSIS OF INV DUP(15) CHROMOSOMES, USING PROBES SPECIFIC FAR THE PRADER-WILLI ANGELMAN SYNDROME REGION - CLINICAL IMPLICATIONS/
Authors: LEANACOX J JENKINS L PALMER CG PLATTNER R SHEPPARD L FLEJTER WL ZACKOWSKI J TSIEN F SCHWARTZ S
Citation: J. Leanacox et al., MOLECULAR CYTOGENETIC ANALYSIS OF INV DUP(15) CHROMOSOMES, USING PROBES SPECIFIC FAR THE PRADER-WILLI ANGELMAN SYNDROME REGION - CLINICAL IMPLICATIONS/, American journal of human genetics, 54(5), 1994, pp. 748-756
MOLECULAR CYTOGENETIC ANALYSIS OF INV DUP(15) CHROMOSOMES
Authors: LEANACOX J JENKINS L PALMER C PLATTNER R SHEPPARD L FLEJTER W ZACKOWSKI J SHAPIRA E SCHWARTZ S
Citation: J. Leanacox et al., MOLECULAR CYTOGENETIC ANALYSIS OF INV DUP(15) CHROMOSOMES, Cytogenetics and cell genetics, 63(4), 1993, pp. 255-255
FLUORESCENT IN-SITU HYBRIDIZATION (FISH) - A NEW APPLICATION IN THE DELINEATION OF TRUE VS PSEUDOMOSAICISM IN PRENATAL-DIAGNOSIS
Authors: SCHWARTZ S LEANACOX J
Citation: S. Schwartz et J. Leanacox, FLUORESCENT IN-SITU HYBRIDIZATION (FISH) - A NEW APPLICATION IN THE DELINEATION OF TRUE VS PSEUDOMOSAICISM IN PRENATAL-DIAGNOSIS, Prenatal diagnosis, 13(8), 1993, pp. 661-670
CYTOGENETIC STUDIES OF PRIMARY CULTURES OF ESOPHAGEAL SQUAMOUS-CELL CARCINOMA
Authors: ROSENBLUMVOS LS MELTZER SJ LEANACOX J SCHWARTZ S
Citation: Ls. Rosenblumvos et al., CYTOGENETIC STUDIES OF PRIMARY CULTURES OF ESOPHAGEAL SQUAMOUS-CELL CARCINOMA, Cancer genetics and cytogenetics, 70(2), 1993, pp. 127-131
CLARIFICATION OF SUBTLE RECIPROCAL REARRANGEMENTS USING FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: SULLIVAN BA LEANACOX J SCHWARTZ S
Citation: Ba. Sullivan et al., CLARIFICATION OF SUBTLE RECIPROCAL REARRANGEMENTS USING FLUORESCENCE IN-SITU HYBRIDIZATION, American journal of medical genetics, 47(2), 1993, pp. 223-230
ANALYSIS OF STRUCTURAL AND CLINICAL HETEROGENEITY OF INV DUP(15) CHROMOSOMES USING MOLECULAR CYTOGENETIC TECHNIQUES
Authors: LEANACOX J SCHWARTZ S
Citation: J. Leanacox et S. Schwartz, ANALYSIS OF STRUCTURAL AND CLINICAL HETEROGENEITY OF INV DUP(15) CHROMOSOMES USING MOLECULAR CYTOGENETIC TECHNIQUES, American journal of human genetics, 53(3), 1993, pp. 124-124
IDENTIFICATION OF SUPERNUMERARY AUTOSOMAL CHROMOSOMES AND UNBALANCED DE-NOVO REARRANGEMENTS WITH FISH - EXPERIENCE WITH 78 CASES
Authors: SCHWARTZ S LEANACOX J DEPINET TW POWERS V WILLARD HF SULLIVAN BA
Citation: S. Schwartz et al., IDENTIFICATION OF SUPERNUMERARY AUTOSOMAL CHROMOSOMES AND UNBALANCED DE-NOVO REARRANGEMENTS WITH FISH - EXPERIENCE WITH 78 CASES, American journal of human genetics, 53(3), 1993, pp. 257-257
CHARACTERIZATION OF DENOVO DUPLICATIONS IN 8 PATIENTS BY USING FLUORESCENCE INSITU HYBRIDIZATION WITH CHROMOSOME-SPECIFIC DNA LIBRARIES
Authors: LEANACOX J LEVIN S SURANA R WULFSBERG E KEENE CL RAFFEL LJ SULLIVAN B SCHWARTZ S
Citation: J. Leanacox et al., CHARACTERIZATION OF DENOVO DUPLICATIONS IN 8 PATIENTS BY USING FLUORESCENCE INSITU HYBRIDIZATION WITH CHROMOSOME-SPECIFIC DNA LIBRARIES, American journal of human genetics, 52(6), 1993, pp. 1067-1073
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