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Results: 1-19 |
Results: 19
OXIDATIVE DNA-DAMAGE AND CYTOGENETIC EFFECTS IN-FLIGHT ENGINEERS EXPOSED TO COSMIC-RADIATION
Authors: ZWINGMANN IH WELLE IJ VANHERWIJNEN M ENGELEN JJM SCHILDERMAN PAEL SMID T KLEINJANS JCS
Citation: Ih. Zwingmann et al., OXIDATIVE DNA-DAMAGE AND CYTOGENETIC EFFECTS IN-FLIGHT ENGINEERS EXPOSED TO COSMIC-RADIATION, Environmental and molecular mutagenesis, 32(2), 1998, pp. 121-129
CHARACTERIZATION OF A DE-NOVO UNBALANCED TRANSLOCATION T(14Q18Q) USING MICRODISSECTION AND FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: ENGELEN JJM LOOTS WJG ALBRECHTS JCM PLOMP AS VANDERMEER SB VLES JSH HAMERS GJH GERAEDTS JPM
Citation: Jjm. Engelen et al., CHARACTERIZATION OF A DE-NOVO UNBALANCED TRANSLOCATION T(14Q18Q) USING MICRODISSECTION AND FLUORESCENCE IN-SITU HYBRIDIZATION, American journal of medical genetics, 75(4), 1998, pp. 409-413
2 CASES OF PARTIAL TRISOMY 8P AND PARTIAL MONOSOMY 21Q IN A FAMILY WITH A RECIPROCAL TRANSLOCATION (8-21)(P21.1-Q22.3)
Authors: PLOMP AS ENGELEN JJM ALBRECHTS JCM DEDIESMULDERS CEM HAMERS AJH
Citation: As. Plomp et al., 2 CASES OF PARTIAL TRISOMY 8P AND PARTIAL MONOSOMY 21Q IN A FAMILY WITH A RECIPROCAL TRANSLOCATION (8-21)(P21.1-Q22.3), Journal of Medical Genetics, 35(7), 1998, pp. 604-608
A SIMPLE AND EFFICIENT METHOD FOR MICRODISSECTION AND MICROFISH
Authors: ENGELEN JJM ALBRECHTS JCM HAMERS GJH GERAEDTS JPM
Citation: Jjm. Engelen et al., A SIMPLE AND EFFICIENT METHOD FOR MICRODISSECTION AND MICROFISH, Journal of Medical Genetics, 35(4), 1998, pp. 265-268
ASSIGNMENT OF THE HUMAN GENE FOR SMOOTHELIN (SMTN) TO CHROMOSOME 22Q12 BY FLUORESCENCE IN-SITU HYBRIDIZATION AND RADIATION HYBRID MAPPING
Authors: ENGELEN JJM ESTERLING LE ALBRECHTS JCM DETERAWADLEIGH SD VANEYS GJJM
Citation: Jjm. Engelen et al., ASSIGNMENT OF THE HUMAN GENE FOR SMOOTHELIN (SMTN) TO CHROMOSOME 22Q12 BY FLUORESCENCE IN-SITU HYBRIDIZATION AND RADIATION HYBRID MAPPING, Genomics, 43(2), 1997, pp. 245-247
SEVERE FEEDING PROBLEMS AND CONGENITAL LARYNGOSTENOSIS IN A PATIENT WITH 3Q23 DELETION
Authors: CHANDLER KE DEDIESMULDERS CEM ENGELEN JJM SCHRANDER JJP
Citation: Ke. Chandler et al., SEVERE FEEDING PROBLEMS AND CONGENITAL LARYNGOSTENOSIS IN A PATIENT WITH 3Q23 DELETION, European journal of pediatrics, 156(8), 1997, pp. 636-638
IDENTIFICATION OF A MARKER CHROMOSOME IN A CASE OF NON-HODGKIN-LYMPHOMA BY MICRO-FISH
Authors: STEVENSKROEF MJPL ALBRECHTS JCM DIRKS R LONEUS W BOT F ENGELEN JJM HAMERS AJH
Citation: Mjpl. Stevenskroef et al., IDENTIFICATION OF A MARKER CHROMOSOME IN A CASE OF NON-HODGKIN-LYMPHOMA BY MICRO-FISH, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 48-48
APPLICATION OF MICRO-FISH TO DELINEATE DELETIONS
Authors: ENGELEN JJM ALBRECHTS JCM LOOTS WJG HOLLANDERSCROMBACH BHTM HAMERS AJH GERAEDTS JPM
Citation: Jjm. Engelen et al., APPLICATION OF MICRO-FISH TO DELINEATE DELETIONS, Cytogenetics and cell genetics, 75(2-3), 1996, pp. 167-171
11Q DUPLICATION IN A PATIENT WITH PITT-ROGERS-DANKS PHENOTYPE
Authors: DEDIESMULDERS CEM ENGELEN JJM
Citation: Cem. Dediesmulders et Jjm. Engelen, 11Q DUPLICATION IN A PATIENT WITH PITT-ROGERS-DANKS PHENOTYPE, American journal of medical genetics, 66(1), 1996, pp. 116-117
DISCLOSURE OF 5 BREAKPOINTS IN A COMPLEX CHROMOSOME REARRANGEMENT BY MICRODISSECTION AND FISH
Authors: ENGELEN JJM LOOTS WJG ALBRECHTS JCM MOTOH PCC FRYNS JP HAMERS AJH GERAEDTS JPM
Citation: Jjm. Engelen et al., DISCLOSURE OF 5 BREAKPOINTS IN A COMPLEX CHROMOSOME REARRANGEMENT BY MICRODISSECTION AND FISH, Journal of Medical Genetics, 33(7), 1996, pp. 562-566
DELETION OF THE LONG ARM OF CHROMOSOME-6 - 2 NEW PATIENTS AND LITERATURE-REVIEW
Authors: EVERS LJM SCHRANDERSTUMPEL CTRM ENGELEN JJM HOORNTJE TM PULLESHEINTZBERGER CFM SCHRANDER JJP ALBRECHTS JCM PETERS J FRYNS JP
Citation: Ljm. Evers et al., DELETION OF THE LONG ARM OF CHROMOSOME-6 - 2 NEW PATIENTS AND LITERATURE-REVIEW, Clinical genetics, 50(3), 1996, pp. 138-144
MARKER CHROMOSOME IDENTIFICATION BY MICRO-FISH (VOL 49, PG 242, 1996)
Authors: ENGELEN JJM LOOTS WJG MOTOH PCC MOOG U HAMERS GJH
Citation: Jjm. Engelen et al., MARKER CHROMOSOME IDENTIFICATION BY MICRO-FISH (VOL 49, PG 242, 1996), Clinical genetics, 49(6), 1996, pp. 333-334
MARKER CHROMOSOME IDENTIFICATION BY MICRO-FISH
Authors: ENGELEN JJM LOOTS WJG MOTOH PCC MOOG U HAMERS GJH GERAEDTS JPM
Citation: Jjm. Engelen et al., MARKER CHROMOSOME IDENTIFICATION BY MICRO-FISH, Clinical genetics, 49(5), 1996, pp. 242-248
INVERSION DUPLICATION OF THE SHORT ARM OF CHROMOSOME-8 - CLINICAL-DATA ON 7 PATIENTS AND REVIEW OF THE LITERATURE
Authors: DEDIESMULDERS CEM ENGELEN JJM SCHRANDERSTUMPEL TRM GOVAERTS LCP DEVRIES B VLES JSH WAGEMANS A SCHIJNSFLEUREN S GILLESSENKAESBACH G FRYNS JP
Citation: Cem. Dediesmulders et al., INVERSION DUPLICATION OF THE SHORT ARM OF CHROMOSOME-8 - CLINICAL-DATA ON 7 PATIENTS AND REVIEW OF THE LITERATURE, American journal of medical genetics, 59(3), 1995, pp. 369-374
FAMILIAL PARTIAL TRISOMY-8P WITHOUT DYSMORPHIC FEATURES AND ONLY MILDMENTAL-RETARDATION
Authors: ENGELEN JJM DEDIESMULDERS CEM SIJSTERMANS JMJ MEERS LEC ALBRECHTS JCM HAMERS AJH
Citation: Jjm. Engelen et al., FAMILIAL PARTIAL TRISOMY-8P WITHOUT DYSMORPHIC FEATURES AND ONLY MILDMENTAL-RETARDATION, Journal of Medical Genetics, 32(10), 1995, pp. 792-795
A DELETION OF 1.6 KB PROXIMAL TO THE CGG REPEAT OF THE FMR1 GENE CAUSES THE CLINICAL PHENOTYPE OF THE FRAGILE X SYNDROME
Authors: MEIJER H DEGRAAFF E MERCKX DML JONGBLOED RJE DEDIESMULDERS CEM ENGELEN JJM FRYNS JP CURFS PMG OOSTRA BA
Citation: H. Meijer et al., A DELETION OF 1.6 KB PROXIMAL TO THE CGG REPEAT OF THE FMR1 GENE CAUSES THE CLINICAL PHENOTYPE OF THE FRAGILE X SYNDROME, Human molecular genetics, 3(4), 1994, pp. 615-620
MOSAIC TETRASOMY 8P IN 2 PATIENTS - CLINICAL-DATA AND REVIEW OF THE LITERATURE
Authors: SCHRANDERSTUMPEL CTRM GOVAERTS CP ENGELEN JJM VANDERBLIJPHILIPSEN M BORGHGRAEF M LOOTS WJG PETERS JJM RIJNVOS WPM SMEETS DFCM FRYNS JP
Citation: Ctrm. Schranderstumpel et al., MOSAIC TETRASOMY 8P IN 2 PATIENTS - CLINICAL-DATA AND REVIEW OF THE LITERATURE, American journal of medical genetics, 50(4), 1994, pp. 377-380
PARTIAL TRISOMY OF THE SHORT ARM OF CHROMOSOME-18 DUE TO INVERSION DUPLICATION AND DIRECT DUPLICATION
Authors: MOOG U ENGELEN JJM DEDIESMULDERS CEM ALBRECHTS JCM LONEUS WH HAAGEN AAM RAVEN EJM HAMERS AJH
Citation: U. Moog et al., PARTIAL TRISOMY OF THE SHORT ARM OF CHROMOSOME-18 DUE TO INVERSION DUPLICATION AND DIRECT DUPLICATION, Clinical genetics, 46(6), 1994, pp. 423-429
PARTIAL TRISOMY AND MONOSOMY 8P DUE TO INVERSION DUPLICATION
Authors: ENGELEN JJM DEDIESMULDERS CEM FRYNS JP HOOVERS JMN ALBRECHTS JCM LOOTS WJG JACOBS ME HAMERS AJH
Citation: Jjm. Engelen et al., PARTIAL TRISOMY AND MONOSOMY 8P DUE TO INVERSION DUPLICATION, Clinical genetics, 45(4), 1994, pp. 203-207
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