AAAAAA

   
Results: 1-9 |
Results: 9
CRANIAL BASE IN PATIENTS WITH CRI-DU-CHAT SYNDROME
Authors: KJAER I NIEBUHR E
Citation: I. Kjaer et E. Niebuhr, CRANIAL BASE IN PATIENTS WITH CRI-DU-CHAT SYNDROME, Journal of dental research, 77, 1998, pp. 2066-2066
MOLECULAR CYTOGENETIC ANALYSIS OF A NONTUMORIGENIC HUMAN BREAST EPITHELIAL-CELL LINE THAT EVENTUALLY TURNS TUMORIGENIC - VALIDATION OF AN ANALYTICAL APPROACH COMBINING KARYOTYPING, COMPARATIVE GENOMIC HYBRIDIZATION, CHROMOSOME PAINTING, AND SINGLE-LOCUS FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: NIELSEN KV NIEBUHR E EJLERTSEN B HOLSTEBROE S MADSEN MW BRIAND P MOURIDSEN HT BOLUND L
Citation: Kv. Nielsen et al., MOLECULAR CYTOGENETIC ANALYSIS OF A NONTUMORIGENIC HUMAN BREAST EPITHELIAL-CELL LINE THAT EVENTUALLY TURNS TUMORIGENIC - VALIDATION OF AN ANALYTICAL APPROACH COMBINING KARYOTYPING, COMPARATIVE GENOMIC HYBRIDIZATION, CHROMOSOME PAINTING, AND SINGLE-LOCUS FLUORESCENCE IN-SITU HYBRIDIZATION, Genes, chromosomes & cancer, 20(1), 1997, pp. 30-37
CAG REPEAT EXPANSION IN AUTOSOMAL-DOMINANT PURE SPASTIC PARAPLEGIA LINKED TO CHROMOSOME 2P21-P24
Authors: NIELSEN JE KOEFOED P ABELL K HASHOLT L EIBERG H FENGER K NIEBUHR E SORENSEN SA
Citation: Je. Nielsen et al., CAG REPEAT EXPANSION IN AUTOSOMAL-DOMINANT PURE SPASTIC PARAPLEGIA LINKED TO CHROMOSOME 2P21-P24, Human molecular genetics, 6(11), 1997, pp. 1811-1816
EXTREME VARIANT OF THE SHORT ARM OF CHROMOSOME-15
Authors: FRIEDRICH U CAPRANI M NIEBUHR E THERKELSEN AJ JORGENSEN AL
Citation: U. Friedrich et al., EXTREME VARIANT OF THE SHORT ARM OF CHROMOSOME-15, Human genetics, 97(6), 1996, pp. 710-713
A 5P-SYNDROME PATIENT WITH 2 DIFFERENT DE-NOVO DELETIONS
Authors: YANG H NIEBUHR A ZHANG X LIU G HUANG S LO W NIEBUHR E
Citation: H. Yang et al., A 5P-SYNDROME PATIENT WITH 2 DIFFERENT DE-NOVO DELETIONS, American journal of human genetics, 57(4), 1995, pp. 738-738
MOLECULAR DEFINITION OF DELETIONS OF DIFFERENT SEGMENTS OF DISTAL 5P THAT RESULT IN DISTINCT PHENOTYPIC FEATURES
Authors: CHURCH DM BENGTSSON U NIELSEN KV WASMUTH JJ NIEBUHR E
Citation: Dm. Church et al., MOLECULAR DEFINITION OF DELETIONS OF DIFFERENT SEGMENTS OF DISTAL 5P THAT RESULT IN DISTINCT PHENOTYPIC FEATURES, American journal of human genetics, 56(5), 1995, pp. 1162-1172
FAMILIAL ADENOMATOUS POLYPOSIS (FAP) - FREQUENCY, PENETRANCE, AND MUTATION-RATE
Authors: BISGAARD ML FENGER K BULOW S NIEBUHR E MOHR J
Citation: Ml. Bisgaard et al., FAMILIAL ADENOMATOUS POLYPOSIS (FAP) - FREQUENCY, PENETRANCE, AND MUTATION-RATE, Human mutation, 3(2), 1994, pp. 121-125
AN EPIDEMIOLOGIC-STUDY OF HIRSCHSPRUNGS-DISEASE AND ADDITIONAL ANOMALIES
Authors: RUSSELL MB RUSSELL CA NIEBUHR E
Citation: Mb. Russell et al., AN EPIDEMIOLOGIC-STUDY OF HIRSCHSPRUNGS-DISEASE AND ADDITIONAL ANOMALIES, Acta paediatrica, 83(1), 1994, pp. 68-71
FAMILIAL OCCURRENCE OF HIRSCHSPRUNGS-DISEASE
Authors: RUSSELL MB RUSSELL CA FENGER K NIEBUHR E
Citation: Mb. Russell et al., FAMILIAL OCCURRENCE OF HIRSCHSPRUNGS-DISEASE, Clinical genetics, 45(5), 1994, pp. 231-235
Risultati: 1-9 |