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Results: 1-23 |
Results: 23
LOCALIZATION OF A FANCONI-ANEMIA GENE TO CHROMOSOME 9P
Authors: SAAR K SCHINDLER D WEGNER RD REIS A WIENKER TF HOEHN H JOENJE H SPERLING K DIGWEED M
Citation: K. Saar et al., LOCALIZATION OF A FANCONI-ANEMIA GENE TO CHROMOSOME 9P, European journal of human genetics, 6(5), 1998, pp. 501-508
MUTATION ANALYSIS IN THE ATM GENE OF 67 ATAXIA-TELANGIECTASIA (A-T) PATIENTS IN GERMANY
Authors: SCHINDLER D BAUMER A BERNTHALER U SENNEFELDER H BROHM M WEBER BHF SANDOVAL N PLATZER M ROSENTHAL A SHILOH Y WEGNER RD SPERLING K DOERK T BENDIX R SKAWRAN B STUHRMANNSPANGENBERG M
Citation: D. Schindler et al., MUTATION ANALYSIS IN THE ATM GENE OF 67 ATAXIA-TELANGIECTASIA (A-T) PATIENTS IN GERMANY, European journal of human genetics, 6, 1998, pp. 4237-4237
CHARACTERIZATION OF CELL-CYCLE CHECKPOINT RESPONSES AFTER IONIZING-RADIATION IN NIJMEGEN BREAKAGE SYNDROME CELLS
Authors: YAMAZAKI V WEGNER RD KIRCHGESSNER CU
Citation: V. Yamazaki et al., CHARACTERIZATION OF CELL-CYCLE CHECKPOINT RESPONSES AFTER IONIZING-RADIATION IN NIJMEGEN BREAKAGE SYNDROME CELLS, Cancer research, 58(11), 1998, pp. 2316-2322
PRENATAL-DIAGNOSIS IN GERMANY
Authors: WEGNER RD BECKER R
Citation: Rd. Wegner et R. Becker, PRENATAL-DIAGNOSIS IN GERMANY, European journal of human genetics, 5, 1997, pp. 32-38
LINKAGE STUDIES EXCLUDE THE AT-V GENE(S) FROM THE TRANSLOCATION BREAKPOINTS IN AN AT-V PATIENT
Authors: CHRZANOWSKA K STUMM M BIALECKA M SAAR K BERNATOWSKAMATUSZKIEWICZ E MICHALKIEWICZ J BARSZCZ S REIS A WEGNER RD
Citation: K. Chrzanowska et al., LINKAGE STUDIES EXCLUDE THE AT-V GENE(S) FROM THE TRANSLOCATION BREAKPOINTS IN AN AT-V PATIENT, Clinical genetics, 51(5), 1997, pp. 309-313
NONCOMPLEMENTATION OF RADIATION-INDUCED CHROMOSOME-ABERRATIONS IN ATAXIA-TELANGIECTASIA ATAXIA-TELANGIECTASIA-VARIANT HETERODIKARYONS/
Authors: STUMM M SPERLING K WEGNER RD
Citation: M. Stumm et al., NONCOMPLEMENTATION OF RADIATION-INDUCED CHROMOSOME-ABERRATIONS IN ATAXIA-TELANGIECTASIA ATAXIA-TELANGIECTASIA-VARIANT HETERODIKARYONS/, American journal of human genetics, 60(5), 1997, pp. 1246-1251
THE GENE FOR THE ATAXIA-TELANGIECTASIA VARIANT, NIJMEGEN BREAKAGE SYNDROME, MAPS TO A 1-CM INTERVAL ON CHROMOSOME 8Q21
Authors: SAAR K CHRZANOWSKA KH STUMM M JUNG M NURNBERG G WIENKER TF SEEMANOVA E WEGNER RD REIS A SPERLING K
Citation: K. Saar et al., THE GENE FOR THE ATAXIA-TELANGIECTASIA VARIANT, NIJMEGEN BREAKAGE SYNDROME, MAPS TO A 1-CM INTERVAL ON CHROMOSOME 8Q21, American journal of human genetics, 60(3), 1997, pp. 605-610
LOCALIZATION OF THE GENE DEFECT FOR THE NEVOID BASAL-CELL CARCINOMA SYNDROME (GORLIN-GOLTZ SYNDROME) AND OTHER CYTOLOGICAL INVESTIGATIONS IN ONE FAMILY
Authors: LINSS G GEBEL E REIS A WEGNER RD PRUTZ D
Citation: G. Linss et al., LOCALIZATION OF THE GENE DEFECT FOR THE NEVOID BASAL-CELL CARCINOMA SYNDROME (GORLIN-GOLTZ SYNDROME) AND OTHER CYTOLOGICAL INVESTIGATIONS IN ONE FAMILY, EJD. European journal of dermatology, 6(4), 1996, pp. 262-263
PREDOMINANCE OF NULL MUTATIONS IN ATAXIA-TELANGIECTASIA
Authors: GILAD S KHOSRAVI R SHKEDY D UZIEL T ZIV Y SAVITSKY K ROTMAN G SMITH S CHESSA L JORGENSEN TJ HARNIK R FRYDMAN M SANAL O PORTNOI S GOLDWICZ Z JASPERS NGJ GATTI RA LENOIR G LAVIN MF TATSUMI K WEGNER RD SHILOH Y BARSHIRA A
Citation: S. Gilad et al., PREDOMINANCE OF NULL MUTATIONS IN ATAXIA-TELANGIECTASIA, Human molecular genetics, 5(4), 1996, pp. 433-439
PARTIAL TRISOMY MONOSOMY 6Q IN FETAL CELLS AND CVS LONG-TERM CULTURE NOT PRESENT IN CVS SHORT-TERM CULTURE/
Authors: WEGNER RD SCHROCK E OBLADEN M BECKER R STUMM M SPERLING K
Citation: Rd. Wegner et al., PARTIAL TRISOMY MONOSOMY 6Q IN FETAL CELLS AND CVS LONG-TERM CULTURE NOT PRESENT IN CVS SHORT-TERM CULTURE/, Prenatal diagnosis, 16(8), 1996, pp. 741-748
FANCONI-ANEMIA COMPLEMENTATION GROUP-E - CLINICAL AND CYTOGENETIC DATA OF THE FIRST PATIENT
Authors: WEGNER RD HENRICHS I JOENJE H SCHROEDERKURTH T
Citation: Rd. Wegner et al., FANCONI-ANEMIA COMPLEMENTATION GROUP-E - CLINICAL AND CYTOGENETIC DATA OF THE FIRST PATIENT, Clinical genetics, 50(6), 1996, pp. 479-482
DNA, FISH AND COMPLEMENTATION STUDIES IN ICF SYNDROME - DNA HYPOMETHYLATION OF REPETITIVE AND SINGLE-COPY LOCI AND EVIDENCE FOR A TRANS-ACTING FACTOR
Authors: SCHUFFENHAUER S BARTSCH O STUMM M BUCHHOLZ T PETROPOULOU T KRAFT S BELOHRADSKY B HINKEL GK MEITINGER T WEGNER RD
Citation: S. Schuffenhauer et al., DNA, FISH AND COMPLEMENTATION STUDIES IN ICF SYNDROME - DNA HYPOMETHYLATION OF REPETITIVE AND SINGLE-COPY LOCI AND EVIDENCE FOR A TRANS-ACTING FACTOR, Human genetics, 96(5), 1995, pp. 562-571
CLASSIFICATION OF FANCONI-ANEMIA PATIENTS BY COMPLEMENTATION ANALYSIS- EVIDENCE FOR A 5TH GENETIC SUBTYPE
Authors: JOENJE H TENFOE JRL OOSTRA AB VANBERKEL CGN ROOIMANS MA SCHROEDERKURTH T WEGNER RD GILLE JJP BUCHWALD M ARWERT F
Citation: H. Joenje et al., CLASSIFICATION OF FANCONI-ANEMIA PATIENTS BY COMPLEMENTATION ANALYSIS- EVIDENCE FOR A 5TH GENETIC SUBTYPE, Blood, 86(6), 1995, pp. 2156-2160
THE ATAXIA-TELANGIECTASIA-VARIANT GENE-1 AND GENE-2 ARE DISTINCT FROMTHE ATAXIA-TELANGIECTASIA GENE ON CHROMOSOME-11Q23.1
Authors: STUMM M GATTI RA REIS A UDAR N CHRZANOWSKA K SEEMANOVA E SPERLING K WEGNER RD
Citation: M. Stumm et al., THE ATAXIA-TELANGIECTASIA-VARIANT GENE-1 AND GENE-2 ARE DISTINCT FROMTHE ATAXIA-TELANGIECTASIA GENE ON CHROMOSOME-11Q23.1, American journal of human genetics, 57(4), 1995, pp. 960-962
FALLOUT FROM CHERNOBYL - AUTHORS STAND BY STUDY THAT CHERNOBYL INCREASED TRISOMY-21 IN BERLIN
Authors: SPERLING K PELZ J WEGNER RD DORRIES A GRUTERS A MIKKELSEN M
Citation: K. Sperling et al., FALLOUT FROM CHERNOBYL - AUTHORS STAND BY STUDY THAT CHERNOBYL INCREASED TRISOMY-21 IN BERLIN, BMJ. British medical journal, 309(6964), 1994, pp. 1299-1299
SIGNIFICANT INCREASE IN TRISOMY-21 IN BERLIN 9 MONTHS AFTER THE CHERNOBYL REACTOR ACCIDENT - TEMPORAL CORRELATION OR CAUSAL RELATION
Authors: SPERLING K PELZ J WEGNER RD DORRIES A GRUTERS A MIKKELSEN M
Citation: K. Sperling et al., SIGNIFICANT INCREASE IN TRISOMY-21 IN BERLIN 9 MONTHS AFTER THE CHERNOBYL REACTOR ACCIDENT - TEMPORAL CORRELATION OR CAUSAL RELATION, BMJ. British medical journal, 309(6948), 1994, pp. 158-162
GENETIC HAPLOTYPING OF ATAXIA-TELANGIECTASIA FAMILIES LOCALIZES THE MAJOR GENE TO AN SIMILAR-TO-850 KB REGION ON CHROMOSOME 11Q23.1
Authors: GATTI RA LANGE E ROTMAN G CHEN X UHRHAMMER N LIANG T CHIPLUNKAR S YANG L UDAR N DANDEKAR S SHEIKHAVANDI S WANG Z YANG HM POLIKOW J ELASHOFF M TELETAR M SANAL O CHESSA L MCCONVILLE C TAYLOR M PORRAS O BORRESEN AL WEGNER RD CURRY C GERKEN S LANGE K CONCANNON P SHILOH Y
Citation: Ra. Gatti et al., GENETIC HAPLOTYPING OF ATAXIA-TELANGIECTASIA FAMILIES LOCALIZES THE MAJOR GENE TO AN SIMILAR-TO-850 KB REGION ON CHROMOSOME 11Q23.1, International journal of radiation biology, 66(6), 1994, pp. 57-62
ULERYTHEMA-OPHRYOGENES AND KERATOSIS PILARIS IN A CHILD WITH MONOSOMY18P
Authors: ZOUBOULIS CC STRATAKIS CA RINCK G WEGNER RD GOLLNICK H ORFANOS CE
Citation: Cc. Zouboulis et al., ULERYTHEMA-OPHRYOGENES AND KERATOSIS PILARIS IN A CHILD WITH MONOSOMY18P, Pediatric dermatology, 11(2), 1994, pp. 172-175
PRIMARY INFERTILITY DUE TO MIXED GONADAL- DYSGENESIS - REPORT OF 2 CASES AND REVIEW OF THE LITERATURE
Authors: WEGNER HEH FERSZT A WEGNER RD DIECKMANN KP
Citation: Heh. Wegner et al., PRIMARY INFERTILITY DUE TO MIXED GONADAL- DYSGENESIS - REPORT OF 2 CASES AND REVIEW OF THE LITERATURE, Der Urologe, 33(4), 1994, pp. 342-346
LOW-GRADE NON-HODGKINS-LYMPHOMA AFTER HIGH-GRADE NON-HODGKINS-LYMPHOMA IN A CHILD WITH ATAXIA TELEANGIECTASIA
Authors: OVERBERGSCHMIDT US WEGNER RD BAUMGARTEN E GUNTHER A EBELL W STEIN H VOGEL M HENZE G
Citation: Us. Overbergschmidt et al., LOW-GRADE NON-HODGKINS-LYMPHOMA AFTER HIGH-GRADE NON-HODGKINS-LYMPHOMA IN A CHILD WITH ATAXIA TELEANGIECTASIA, Cancer, 73(5), 1994, pp. 1522-1525
PARTIAL TRISOMY 1Q, AN UNCOMMON CHROMOSOMAL ABERRATION IN ERYTHROLEUKEMIA
Authors: BAUMGARTEN E WEGNER RD FENGLER R KOCH H HENZE G
Citation: E. Baumgarten et al., PARTIAL TRISOMY 1Q, AN UNCOMMON CHROMOSOMAL ABERRATION IN ERYTHROLEUKEMIA, Leukemia & lymphoma, 10(3), 1993, pp. 237-240
CHROMOSOMAL BREAKAGE, ENDOMITOSIS, ENDOREDUPLICATION, AND HYPERSENSITIVITY TOWARD RADIOMIMETRIC AND ALKYLATING-AGENTS - A POSSIBLE NEW AUTOSOMAL RECESSIVE MUTATION IN A GIRL WITH CRANIOSYNOSTOSIS AND MICROCEPHALY
Authors: TOMMERUP N MORTENSEN E NIELSEN MH WEGNER RD SCHINDLER D MIKKELSEN M
Citation: N. Tommerup et al., CHROMOSOMAL BREAKAGE, ENDOMITOSIS, ENDOREDUPLICATION, AND HYPERSENSITIVITY TOWARD RADIOMIMETRIC AND ALKYLATING-AGENTS - A POSSIBLE NEW AUTOSOMAL RECESSIVE MUTATION IN A GIRL WITH CRANIOSYNOSTOSIS AND MICROCEPHALY, Human genetics, 92(4), 1993, pp. 339-346
MIXED GONADAL-DYSGENESIS ASSOCIATED WITH UNILATERAL CAVERNOSAL FIBROSIS AND PRESENTING AS A CYSTIC LOWER ABDOMINAL-MASS
Authors: WEGNER HEH KLAN R WEGNER RD KNISPEL HH FERSZT A DIECKMANN KP
Citation: Heh. Wegner et al., MIXED GONADAL-DYSGENESIS ASSOCIATED WITH UNILATERAL CAVERNOSAL FIBROSIS AND PRESENTING AS A CYSTIC LOWER ABDOMINAL-MASS, European urology, 24(3), 1993, pp. 428-430
Risultati: 1-23 |