Authors:
ELLAWAY C
BUCHHOLZ T
SMITH A
LEONARD H
CHRISTODOULOU J
Citation: C. Ellaway et al., RETT-SYNDROME - SIGNIFICANT CLINICAL OVERLAP WITH ANGELMAN-SYNDROME BUT NOT WITH METHYLATION STATUS, Journal of child neurology, 13(9), 1998, pp. 448-451
Authors:
MANOLI JM
POTVIN C
MUHLER M
WILD U
RESOFSZKI G
BUCHHOLZ T
PAAL Z
Citation: Jm. Manoli et al., EVOLUTION OF THE CATALYTIC ACTIVITY IN PT SULFATED ZIRCONIA CATALYSTS- STRUCTURE, COMPOSITION, AND CATALYTIC PROPERTIES OF THE CATALYST PRECURSOR AND THE CALCINED CATALYST, Journal of catalysis (Print), 178(1), 1998, pp. 338-351
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
Citation: T. Buchholz et al., METHYLATION ANALYSIS AT 3 DIFFERENT LOCI WITHIN THE IMPRINTED REGION OF CHROMOSOME 15Q11-13, American journal of medical genetics, 72(1), 1997, pp. 117-119
Authors:
SANDANAM T
BEANGE H
ROBSON L
WOOLNOUGH H
BUCHHOLZ T
SMITH A
Citation: T. Sandanam et al., MANIFESTATIONS IN INSTITUTIONALIZED ADULTS WITH ANGELMAN SYNDROME DUETO DELETION, American journal of medical genetics, 70(4), 1997, pp. 415-420
Citation: T. Buchholz et Bw. Schulze, ANISOTROPIC EDGE PSEUDODIFFERENTIAL-OPERATORS WITH DISCRETE ASYMPTOTICS, Mathematische Nachrichten, 184, 1997, pp. 73-125
Citation: A. Smith et al., DIAGNOSTIC TESTING FOR PRADER-WILLI AND ANGELMAN SYNDROMES - RESPONSE, American journal of human genetics, 61(1), 1997, pp. 241-244
Authors:
SCHUFFENHAUER S
BUCHHOLZ T
STENGELRUTKOWSKI S
BUITING K
SCHMIDT H
MEITINGER T
Citation: S. Schuffenhauer et al., A FAMILIAL DELETION IN THE PRADER-WILLI-SYNDROME REGION INCLUDING THEIMPRINTING CONTROL REGION, Human mutation, 8(3), 1996, pp. 288-292
Citation: R. Hunt et al., VERIFICATION OF THE PERFORMANCE OF A NEW LIQUID STABILIZED TUMOR-MARKER CONTROL, Clinical chemistry, 42(6), 1996, pp. 677-677
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