Authors:
BUITING K
DITTRICH B
GROSS S
LICH C
FARBER C
BUCHHOLZ T
SMITH E
REIS A
BURGER J
NOTHEN MM
BARTHWITTE U
JANSSEN B
ABELIOVICH D
LERER I
VANDENOUWELAND AMW
HALLEY DJJ
SCHRANDERSTUMPEL C
SMEETS H
MEINECKE P
MALCOLM S
GARDNER A
LALANDE M
NICHOLLS RD
FRIEND K
SCHULZE A
MATTHIJS G
KOKKONEN H
HILBERT P
VANMALDERGEM L
GLOVER G
CARBONELL P
WILLEMS P
GILLESSENKAESBACH G
HORSTHEMKE B
Citation: K. Buiting et al., SPORADIC IMPRINTING DEFECTS IN PRADER-WILLI-SYNDROME AND ANGELMAN-SYNDROME - IMPLICATIONS FOR IMPRINT-SWITCH MODELS, GENETIC-COUNSELING, AND PRENATAL-DIAGNOSIS, American journal of human genetics, 63(1), 1998, pp. 170-180
Authors:
ZESCHNIGK M
SCHMITZ B
DITTRICH B
BUITING K
HORSTHEMKE B
DOERFLER W
Citation: M. Zeschnigk et al., IMPRINTED SEGMENTS IN THE HUMAN GENOME - DIFFERENT DNA METHYLATION PATTERNS IN THE PRADER-WILLI ANGELMAN SYNDROME REGION AS DETERMINED BY THE GENOMIC SEQUENCING METHOD/, Human molecular genetics, 6(3), 1997, pp. 387-395
Authors:
CHAUBON MA
DITTRICH B
ESCUDIE J
RAMDANE H
RANAIVONJATOVO H
SATGE J
Citation: Ma. Chaubon et al., NEW (2,4,6-TRIISOPROPYLPHENYL) HYDROHALOGERMANES, HALOHALOGERMANES AND HYDROHALOGERMANES, Synthesis and reactivity in inorganic and metal-organic chemistry, 27(4), 1997, pp. 519-533
Authors:
BURGER J
BUITING K
DITTRICH B
GROSS S
LICH C
SPERLING K
HORSTHEMKE B
REIS A
Citation: J. Burger et al., DIFFERENT MECHANISMS AND RECURRENCE RISKS OF IMPRINTING DEFECTS IN ANGELMAN-SYNDROME, American journal of human genetics, 61(1), 1997, pp. 88-93
Authors:
DITTRICH B
BUITING K
KORN B
RICKARD S
BUXTON J
SAITOH S
NICHOLLS RD
POUSTKA A
WINTERPACHT A
ZABEL B
HORSTHEMKE B
Citation: B. Dittrich et al., IMPRINT SWITCHING ON HUMAN-CHROMOSOME-15 MAY INVOLVE ALTERNATIVE TRANSCRIPTS OF THE SNRPN GENE, Nature genetics, 14(2), 1996, pp. 163-170
Citation: B. Dittrich et al., PW71 METHYLATION TEST FOR PRADER-WILLI AND ANGELMAN SYNDROMES, American journal of medical genetics, 61(2), 1996, pp. 196-197
Authors:
BUITING K
SAITOH S
GROSS S
DITTRICH B
SCHWARTZ S
NICHOLLS RD
HORSTHEMKE B
Citation: K. Buiting et al., INHERITED MICRODELETIONS IN THE ANGELMAN AND PRADER-WILLI SYNDROMES DEFINE AN IMPRINTING CENTER ON HUMAN-CHROMOSOME-15, Nature genetics, 9(4), 1995, pp. 395-400
Authors:
HORSTHEMKE B
DITTRICH B
KORN B
POUSTKA A
BUITING K
Citation: B. Horsthemke et al., A TRANSCRIPT FROM THE PUTATIVE IMPRINTING CENTER IN THE PRADER-WILLI ANGELMAN SYNDROME REGION, American journal of human genetics, 57(4), 1995, pp. 145-145
Authors:
BUITING K
DITTRICH B
ROBINSON WP
GUITART M
ABELIOVICH D
LERER I
HORSTHEMKE B
Citation: K. Buiting et al., DETECTION OF ABERRANT DNA METHYLATION IN UNIQUE PRADER-WILLI-SYNDROMEPATIENTS AND ITS DIAGNOSTIC IMPLICATIONS, Human molecular genetics, 3(6), 1994, pp. 893-895
Authors:
BUITING K
DITTRICH B
ROBINSON WP
GUITART M
ABELIOVICH D
LERER I
HORSTHEMKE B
Citation: K. Buiting et al., DETECTION OF ABERRANT DNA METHYLATION IN UNIQUE PRADER-WILLI-SYNDROMEPATIENTS AND ITS DIAGNOSTIC IMPLICATIONS (VOL 3, PG 893, 1994), Human molecular genetics, 3(11), 1994, pp. 2092-2092
Authors:
DITTRICH B
BUITING K
GROSS S
HORSTHEMKE B
Citation: B. Dittrich et al., AN INSERTION DELETION POLYMORPHISM AT THE D15S63 LOCUS IN THE CRITICAL PRADER-WILLI-SYNDROME REGION IN 15Q11-13/, Human genetics, 94(5), 1994, pp. 583-584
Citation: B. Horsthemke et al., MOLECULAR CHARACTERIZATION OF THE PRADER-WILLI-SYNDROME CHROMOSOME REGION AND DETECTION OF PARENT-OF-ORIGIN SPECIFIC DNA METHYLATION, Cytogenetics and cell genetics, 67(1), 1994, pp. 16-17
Authors:
VOLLACK KU
DITTRICH B
FERRER A
BORONAT A
BACH TJ
Citation: Ku. Vollack et al., 2 RADISH GENES FOR 3-HYDROXY-3-METHYLGLUTARYL-COA REDUCTASE ISOZYMES COMPLEMENT MEVALONATE AUXOTROPHY IN A YEAST MUTANT AND YIELD MEMBRANE-BOUND ACTIVE ENZYME, Journal of plant physiology, 143(4-5), 1994, pp. 479-487
Authors:
REIS A
DITTRICH B
GREGER V
BUITING K
LALANDE M
GILLESSENKAESBACH G
ANVRET M
HORSTHEMKE B
Citation: A. Reis et al., IMPRINTING MUTATIONS SUGGESTED BY ABNORMAL DNA METHYLATION PATTERNS IN FAMILIAL ANGELMAN AND PRADER-WILLI SYNDROMES, American journal of human genetics, 54(5), 1994, pp. 741-747
Authors:
DITTRICH B
GROSS S
BUITING K
HORSTHEMKE B
Citation: B. Dittrich et al., AN NCII RFLP AT THE D15S63 LOCUS IN THE CRITICAL PRADER-WILLI-SYNDROME REGION IN 15Q11-13, Human molecular genetics, 2(9), 1993, pp. 1509-1509
Authors:
BUITING K
DITTRICH B
GROSS S
GREGER V
LALANDE M
ROBINSON W
MUTIRANGURA A
LEDBETTER D
HORSTHEMKE B
Citation: K. Buiting et al., MOLECULAR DEFINITION OF THE PRADER-WILLI-SYNDROME CHROMOSOME REGION AND ORIENTATION OF THE SNRPN GENE, Human molecular genetics, 2(12), 1993, pp. 1991-1994
Authors:
DITTRICH B
BUITING K
GROSS S
HORSTHEMKE B
Citation: B. Dittrich et al., CHARACTERIZATION OF A METHYLATION IMPRINT IN THE PRADER-WILLI-SYNDROME CHROMOSOME REGION, Human molecular genetics, 2(12), 1993, pp. 1995-1999
Authors:
BODEMANN R
LANGE HJ
LEYA I
MICHEL R
SCHIEKEL T
ROSEL R
HERPERS U
HOFMANN HJ
DITTRICH B
SUTER M
WOLFLI W
HOLMQVIST B
CONDE H
MALMBORG P
Citation: R. Bodemann et al., PRODUCTION OF RESIDUAL NUCLEI BY PROTON-INDUCED REACTIONS ON C, N, O,MG, AL AND SI, Nuclear instruments & methods in physics research. Section B, Beam interactions with materials and atoms, 82(1), 1993, pp. 9-31
Authors:
DITTRICH B
BUITING K
GILLESSENKAESBACH G
HORSTHEMKE B
Citation: B. Dittrich et al., PARENT-OF-ORIGIN SPECIFIC DNA METHYLATION AND IMPRINTING MUTATIONS INTHE PRADER-WILLI-SYNDROME, American journal of human genetics, 53(3), 1993, pp. 1151-1151