Announcements (Deutsch)
In:
Human Genetics
;
61
, 3
; 279-279
;
1982
-
ISSN:
- Aufsatz (Zeitschrift) / Elektronische Ressource
-
Titel:Announcements
-
Erschienen in:Human Genetics ; 61, 3 ; 279-279
-
Verlag:
- Neue Suche nach: Springer Berlin Heidelberg
- Neue Suche nach: Springer
-
Erscheinungsort:Berlin
-
Erscheinungsdatum:1982
-
ISSN:
-
ZDBID:
-
DOI:
-
Medientyp:Aufsatz (Zeitschrift)
-
Format:Elektronische Ressource
-
Sprache:Deutsch
- Neue Suche nach: 44.48
- Weitere Informationen zu Basisklassifikation
-
Schlagwörter:
-
Klassifikation:
BKL: 44.48 Medizinische Genetik -
Datenquelle:
Inhaltsverzeichnis – Band 61, Ausgabe 3
Zeige alle Jahrgänge und Ausgaben
Die Inhaltsverzeichnisse werden automatisch erzeugt und basieren auf den im Index des TIB-Portals verfügbaren Einzelnachweisen der enthaltenen Beiträge. Die Anzeige der Inhaltsverzeichnisse kann daher unvollständig oder lückenhaft sein.
- 181
-
Homozygous Robertsonian translocations in a fetus with 44 chromosomesRockman-Greenberg, C. / Ray, M. / Evans, J. A. / Canning, N. / Hamerton, J. L. et al. | 1982
- 185
-
Diphenoloxidases in various forms of myopathy which are transmitted by different genetic mechanismsDemos, Jean J. / Tuil, David G. / Katz, Pierre C. et al. | 1982
- 190
-
Nondisjunction and chromosome breakage in mouse oocytes after various X-ray dosesHansmann, I. / Jenderny, J. / Probeck, H. D. et al. | 1982
- 193
-
Population genetical aspects of primary congenital glaucoma. I. Incidence, prevalence, gene frequency, and age of onsetGenčík, A. / Genčíkova, A. / Ferák, V. et al. | 1982
- 198
-
Population genetic aspects of primary congenital glaucoma. II. Fitness, parental consanguinity, founder effectFerák, V. / Genčík, A. / Genčíkova, A. et al. | 1982
- 201
-
Similar chromosomal abnormalities in several retinoblastomasKusnetsova, Lundmila E. / Prigogina, Elena L. / Pogosianz, Helen E. / Belkina, Bella M. et al. | 1982
- 205
-
Detection of carriers for duchenne muscular dystrophy. Quality control of creatine kinase assayPlauchu, H. / Junien, C. / Maire, I. / Said, R. / Gozlan, R. / Lalouel, J. M. et al. | 1982
- 210
-
Polymorphism of the haptoglobin peptides by isoelectric focusing electrophoresis and isoelectric point determinationsShibata, K. / Constans, J. / Viau, M. / Matsumoto, H. et al. | 1982
- 215
-
Prenatal diagnosis and outcome of pregnancy in 2036 women investigated by amniocentesisSquire, Jeremy A. / Nauth, Lesley / Ridler, Michael A. C. / Sutton, Simon / Timberlake, Carol et al. | 1982
- 223
-
Analysis of the breakpoints in translocation (15;17) Observed in 4 patients with acute promyelocytic leukemiaHagemeijer, A. / Löwenberg, B. / Abels, J. et al. | 1982
- 228
-
Cytogenetic toxicity of antitumor platinum compounds in Fanconi's anemiaPoll, Everdina H. A. / Arwert, Fré / Joenje, Hans / Eriksson, Aldur W. et al. | 1982
- 231
-
Somatic cell hybridization studies on the genetic regulation and allelic mutations in metachromatic leukodystrophyChang, Patricia L. / Rosa, Nadia E. / Davidson, Ronald G. et al. | 1982
- 236
-
The DNA tumor virus SV 40 induces gene mutations in human cells. Reversion of HPRT deficiencyLübbe, Lieselotte / Strauss, Michael / Scherneck, Siegfried / Geissler, Erhard et al. | 1982
- 242
-
Isoelectric focusing of human red cell phosphoglucomutase ($ PGM_{1} $). Phenotype distribution in the population of Tuscany and two hereditary variantsBargagna, M. / Abbagnale, L. et al. | 1982
- 246
-
Interphase flow-cytogenetics: Correlation of DNA fluorescence to aneuploidy in human fibroblast culturesRabinovitch, P. S. / Martin, G. M. / Hoehn, H. et al. | 1982
- 250
-
The mode of inheritance of ovalocytosis/elliptocytosis in Malaysian Orang Asli familiesFix, Alan G. / Baer, Adela S. / Lie-Injo, L. E. et al. | 1982
- 254
-
The expression of fragile X chromosomes in members of the same family at different times of examinationEberle, Gertrud / Zankl, Merve / Zankl, Heinrich et al. | 1982
- 256
-
A red cell pyruvate kinase mutant with normal L-type PK in the liverEtiemble, Jeanne / Picat, Christiane / Boivin, Pierre et al. | 1982
- 259
-
Lack of effect of vitamin C on the incidence of chromosome anomalies induced by influenza virus in germ cells of micePichan, Kalpagam / Polasa, Hanumanlu et al. | 1982
- 262
-
Transmission of fragile (X)(q27) from normal male(s)Fryns, J. P. / Van Den Berghe, H. et al. | 1982
- 264
-
Deletion of 13q in two patients with retinoblastoma, one probably due to 13q- mosaicism in the motherMichalová, Kyra / Klouček, František / Musilová, Jana et al. | 1982
- 267
-
Dentition of a 48,XYY,+21 maleTownsend, Grant et al. | 1982
- 269
-
Lethal, neonatal, short-limbed platyspondylic dwarfism. A further variant?Winter, R. M. / Thompson, E. M. et al. | 1982
- 273
-
A variant of the fra(X) syndromeBühler, Erica M. / Hadziselimovic, Faruk / Pira, Ulla et al. | 1982
- 277
-
A new case of satellited Yq chromosomeMartín, M. J. / Rodriguez, T. / Abrisqueta, J. A. et al. | 1982
- 277
-
Interstitial deletion 46,XY,del(1)(q23q25)Martin, A. O. / Simpson, J. Leigh et al. | 1982
- 279
-
Announcements| 1982