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Results:
1-11
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Results: 11
Authors:
TOENNIES H
MULLER D
HUMMEL S
HERRMANN H
SPERLING K
NEITZEL H
Citation: H. Toennies et al., CHROMOSOME ANALYSIS OF A 262 YEARS PRESERVED FETUS WITH MULTIPLE CONGENITAL-MALFORMATIONS - FIRST APPLICATION OF COMPARATIVE GENOMIC HYBRIDIZATION TO ANCIENT DNA, European journal of human genetics, 6, 1998, pp. 2055-2055
Authors:
NEITZEL H
KALSCHEUER V
HENSCHEL S
DIGWEED M
SPERLING K
Citation: H. Neitzel et al., BETA-HETEROCHROMATIN IN MAMMALS - EVIDENCE FROM STUDIES IN MICROTUS-AGRESTIS BASED ON THE EXTENSIVE ACCUMULATION OF L1 AND NON-L1 RETROPOSONS IN THE HETEROCHROMATIN, Cytogenetics and cell genetics, 80(1-4), 1998, pp. 165-172
Authors:
YANG F
OBRIEN PCM
WIENBERG J
NEITZEL H
LIN CC
FERGUSONSMITH MA
Citation: F. Yang et al., CHROMOSOMAL EVOLUTION OF THE CHINESE MUNTJAC (MUNTIACUS-REEVESI), Chromosoma, 106(1), 1997, pp. 37-43
Authors:
SCHUSTER H
WIENKER TF
BAHRING S
BILGINTURAN N
TOKA HR
NEITZEL H
JESCHKE E
TOKA O
GILBERT D
LOWE A
OTT J
HALLER H
LUFT FC
Citation: H. Schuster et al., SEVERE AUTOSOMAL-DOMINANT HYPERTENSION AND BRACHYDACTYLY IN A UNIQUE TURKISH KINDRED MAPS TO HUMAN-CHROMOSOME-12, Nature genetics, 13(1), 1996, pp. 98-100
Authors:
SANDER T
HILDMANN T
JANZ D
WIENKER TF
BIANCHI A
BAUER G
SAILER U
SCARAMELLI A
NEITZEL H
SCHMITZ B
BAILEY MES
BECKMANNAGETTA G
JOHNSON KJ
DARLISON MG
Citation: T. Sander et al., EXCLUSION OF LINKAGE BETWEEN IDIOPATHIC GENERALIZED EPILEPSIES AND THE GABA(A) RECEPTOR ALPHA-1 AND GAMMA-2 SUBUNIT GENE-CLUSTER ON CHROMOSOME-5, Epilepsy research, 23(3), 1996, pp. 235-244
Authors:
KALSCHEUER V
SINGH AP
NANDA I
SPERLING K
NEITZEL H
Citation: V. Kalscheuer et al., EVOLUTION OF THE GONOSOMAL HETEROCHROMATIN OF MICROTUS-AGRESTIS - RAPID AMPLIFICATION OF A LARGE, MULTIMERIC, REPEAT UNIT CONTAINING A 3.0-KB (GATA)(11)-POSITIVE, MIDDLE REPETITIVE ELEMENT, Cytogenetics and cell genetics, 73(3), 1996, pp. 171-178
Authors:
SANDER T
HILDMANN T
WIENKER TF
RAMEL C
BECKMANNAGETTA G
BIANCHI A
SAILER U
BEREK K
BAUER G
NEITZEL H
SCHMITZ B
DURNER M
JOHNSON KJ
JANZ D
Citation: T. Sander et al., COMMON SUBTYPES OF IDIOPATHIC GENERALIZED EPILEPSIES - LACK OF LINKAGE TO D20S19 CLOSE TO CANDIDATE LOCI (EBN1, EEGV1) ON CHROMOSOME-20, American journal of medical genetics, 67(1), 1996, pp. 31-39
Authors:
SANDER T
HILDMANN T
JANZ D
WIENKER TF
NEITZEL H
BIANCHI A
BAUER G
SAILER U
BEREK K
SCHMITZ B
BECKMANNAGETTA G
Citation: T. Sander et al., THE PHENOTYPIC SPECTRUM RELATED TO THE HUMAN EPILEPSY SUSCEPTIBILITY GENE EJM1, Annals of neurology, 38(2), 1995, pp. 210-217
Authors:
SANDER T
JANZ D
RAMEL C
ROSS CA
PASCHEN W
HILDMANN T
WIENKER TF
BIANCHI A
BAUER G
SAILER U
BEREK K
NEITZEL H
VOLZ A
ZIEGLER A
SCHMITZ B
BECKMANNAGETTA G
Citation: T. Sander et al., REFINEMENT OF MAP POSITION OF THE HUMAN GLUR6 KAINATE RECEPTOR GENE (GRIK2) AND LACK OF ASSOCIATION AND LINKAGE WITH IDIOPATHIC GENERALIZEDEPILEPSIES, Neurology, 45(9), 1995, pp. 1713-1720
Authors:
VONBAEYER H
NEITZEL H
NUNDEL M
RIEDEL E
SCHULTIS HK
Citation: H. Vonbaeyer et al., COVALENT COUPLING OF NUCLEOSIDES TO LOW-DENSITY-LIPOPROTEIN (LDL) GENERATES MACROPHAGE SPECIFIC (DRUG)-CARRIERS, International journal of clinical pharmacology, therapy and toxicology, 31(8), 1993, pp. 382-386
Authors:
NEITZEL H
Citation: H. Neitzel, THE ENTRANCES OF ATHENA AND APOLLO IN THE 'EUMENIDEN' OF AESCHYLUS (397-414 AND 566-584), Hermes, 121(2), 1993, pp. 139-158
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