| Screening for minute deletions in patients with suspected cri-du-chat syndrome and apparently normal karyotype |
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| Cytogenetic investigation of meiotic chromosomes of male mice after chronic caffeine treatment |
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| Famili�re 2/C-Translokation: 46,XY t (2p-; Cp+) und 46,XX Cp+ |
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| Double chromosomal aberration |
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| Studies on the population genetics of the ceruloplasmin polymorphism |
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| Population genetic studies on pseudocholinesterase polymorphism in Germany, ?zechoslovakia, Finland and among Laps |
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|
✓ |
|
Germany, Czechoslovakia, Finland, Laps |
| Isoamylases in blood donors |
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| Zur Ultrastruktur der Chromosomen des Menschen |
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| Effect of LSD-25 on mitotic and meiotic chromosomes of mice and monkeys |
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| Cytogenetische, immunologische und cytologische Familienuntersuchungen bei Bloom-Syndrom |
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| Zur Gen-Lokalisierung der Glucose-6-Phosphat-Dehydrogenase bei V�geln |
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| Kreatin-Phosphokinase-Aktivit�t im Serum bei Konduktorinnen der progressive Muskeldystrophie vom Typ Duchenne |
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|
|
| The incidence of some inherited EEG variants in normal Japanese and German males |
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|
✓ |
|
Japanese; German |
| A search for dominant mutations in F1 progeny of male mice treated with trenimone (triethyleneiminobenzoquinone-1,4) |
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| A case of translocation D-, t(lp+) |
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| Die bedeutung der Assoziation satellitentragender Chromosomen |
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| Spontaneous fragility of an abnormally wide secondary constriction region in a human chromosome No. 9 |
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| Quantitative Untersuchungen �ber Chromosomenmutationen bei menschlichen Leukocyten durch Cyclophosphamid nach Aktivierung an Leberschnitten |
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| Genetische Untersuchungen bei angeborener organischer subvalvul�rer Aortenstenose |
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| Heterologe Reaktionen von S�ugetierseren mit monospezifischen Antihumanseren |
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| Pseudocholinesterases and human red cell acid phosphatases in Koreans |
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| Zur formalen Genetik von Isoenzymen, dargestellt am Beispiel der 6-PGD (EC: 1.1.1.44) |
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| Strukturanomalie (inv (p-q+)?) eines Chromosoms der Gruppe C+X bei einem jungen mit multiplen dysplasien und dissoziationen der psychischen entwicklung |
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| The genetic aspect of the familial amyloidotic polyneuropathy |
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| Phenotypical variants of pseudocholinesterase in myeloma patients |
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| Cytologische Untersuchungen an einem menschlichen Abortus mit vorwiegend tetraploiden Zellen in vitro |
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| Chromosomenaberrationen durch Myleran in menschlichen Leukocyten in vitro |
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| Does caffeine induce dominant lethal mutations in mice? |
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| Adenosine deaminase polymorphism (EC: 3.5.4.4): Formal genetics and linkage relations |
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|
|
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| Albumin cayemite: A Negro plasma albumin variant |
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|
✓ |
|
Negro |
| Polyploidization in the fish family Cyprinidae, order Cypriniformes |
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|
|
| Blood cell pyruvate kinase activity in translocation Down's syndrome |
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| Argininbelastungstest bei Huntingtonscher Chorea |
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|
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| Ring chromosome 18 (46,XX,18r) |
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|
|
|
| Phosphoglucomutase (EC 2.7.5.1.) and adenylate kinase (EC 2.7.4.3.) typings in Koreans and Irish |
|
|
|
|
|
|
✓ |
|
Koreans and Irish |
| Zur Frage der Verteilung des Rh(D)-Faktors bei erstgeborenen und nachgeborenen Kindern |
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|
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|
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| Further family studies on the genetic control of ?2-glycoprotein I concentration in human serum |
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|
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| Studies on the Xh antigen in human serum |
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|
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| ABO blood groups, leprosy, and serum proteins |
|
|
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|
|
|
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| Population genetics of adenosine deaminase (EC: 3.5.4.4): Gene frequencies in Southwestern Germany |
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|
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|
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|
|
| Zur Populationsgenetik der sauren Phosphatase der Erythrocyten (EC: 3.1.3.1): Ph�notypen- und Allelh�ufigkeiten in der ?SSR |
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|
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| Vergleichende Enzymuntersuchungen im Serum, in Erythrocyten und in Leukocyten von schwachsinnigen Anstaltspatienten |
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|
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| Heterologe Reaktionen von S�ugetierseren mit monospezifischen Antihumanseren Ein Beitrag zur Evolution der Serumproteine |
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|
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|
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|
|
|
| Extra Y chromosomes and epilepsy |
|
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|
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| Famili�res Mosaik mit G-ring |
|
|
|
|
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|
|
| Spontane und chloramphenicolinduzierte Chromosomenmutationen und biochemische Befunde bei zwei F�llen mit Glutathionreduktasemangel (NAD(P)H: Glutathione oxidoreductase, E.C. 1.6.4.2.) |
|
|
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|
|
|
|
|
|
| Chromosomal peculiarities and ?in vitro? examinations in Fanconi's anaemia |
|
|
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|
|
|
|
|
|
| Induction of chromosomal breakage in cultured human leucocytes by luteoskyrin |
|
|
|
|
|
|
|
|
|
| A system for automated chromosome analysis |
|
|
|
|
|
|
|
|
|
| Das XO/XY-Geschlechtschromosomenmosaik |
|
|
|
|
|
|
|
|
|
| Phenotypic variations of haptoglobin Johnson types |
|
|
|
|
|
|
|
|
|
| Lack of association and linkage between ?-thalassemia and some serum protein systems (Gm, Inv, Hp, Gc, and Ag) |
|
|
|
|
|
|
|
|
|
| Polyploidization in the fish family Cyprinidae, order Cypriniformes |
|
|
|
|
|
|
|
|
|
| Isoenzymes and population genetics of sorbit dehydrogenase (EC: 1.1.1.14) in swine (sus scrofa) |
|
|
|
|
|
|
|
|
|
| Zur formalen Genetik der Adenylatkinasen (EC: 2.7.4.3) Hinweis auf Kopplung der loci f�r AK und ABO |
|
|
|
|
|
|
|
|
|
| Relative positions of homologous chromosomes or groups in male and female metaphase figures |
|
|
|
|
|
|
|
|
|
| The genetic load of a human population due to cytostatic agents |
|
|
|
|
|
|
|
|
|
| Die wirkung von Trypaflavin allein und in Kombination mit sichtbarem Licht auf die Chromosomen von HeLa-Zellen und menschliche Leukocyten |
|
|
|
|
|
|
|
|
|
| Tryptophanbelastungstest bei Huntingtonscher Chorea |
|
|
|
|
|
|
|
|
|
| Immunological investigations on the evolution of fibrinogen and plasminogen |
|
|
|
|
|
|
|
|
|
| Biochemical characterization of the ?-chain variant haptoglobin Marburg |
|
|
|
|
|
|
|
|
|
| Partial deletion of the long arm of chromosome 18 |
|
|
|
|
|
|
|
|
|
| Darstellung und Charakterisierung eines Lipoproteins mit Antigenwirksamkeit im Lp-System |
|
|
|
|
|
|
|
|
|
| Untersuchungen �ber die Anordnung der menschlichen Metaphasechromsomen |
|
|
|
|
|
|
|
|
|
| Incidence of glucose-6-phosphate dehydrogenase deficiency in three gujarati populations |
|
|
|
|
|
|
|
|
|
| Beobachtungen zum Mosaizismus beim Cri-du-chat-Syndrom |
|
|
|
|
|
|
|
|
|
| The zygosity in the human HL-A transplantation system |
|
|
|
|
|
|
|
|
|
| Studies on isozymes of sorbitol dehydrogenase in some vertebrate species |
|
|
|
|
|
|
|
|
|
| Mise en �vidence d'un m�canisme g�n�tique contr�lant la synth�se de certaines sous-classes des ?G dans des hypogammaglobulinemies dites acquises |
|
|
|
|
|
|
|
|
|
| Beurteilung des diagnostischen Wertes der finger- und Handleistenmerkmale von Mongoloiden unter Anwendung einer Diskriminanzanalyse |
|
|
|
|
|
|
✓ |
|
Mongoloiden |
| Biostatistische Familienuntersuchungen zur Hautleistenvariabilit�t des Menschen |
|
|
|
|
|
|
|
|
|
| Deletion und Translokation heterochromatischer Chromosomenabschnitte bei Microtus agrestis |
|
|
|
|
|
|
|
|
|
| Verteilung strahleninduzierter Br�che auf den Geschlechtschromosomen von Microtus agrestis |
|
|
|
|
|
|
|
|
|
| Zur Frage der Verteilung der ABO-Blutgruppen bei an Scharlach erkrankten Kindern |
|
|
|
|
|
|
|
|
|
| Gene frequencies of adenylatekinase polymorphism in the Roman population |
|
|
|
|
|
|
|
|
|
| Isozymmuster der Phosphoglucomutase der menschlichen Thrombocyten (Thr.-PGM1) |
|
|
|
|
|
|
|
|
|
| Point mutations and human hemoglobin variants |
|
|
|
|
|
|
|
|
|
| The occurrence of antigenic determinants of human blood proteins in mammalian plasmas |
|
|
|
|
|
|
|
|
|
| Untersuchungen von Proteinpolymorphismen an einer Familie mit geh�uften Chromosomenaberrationen |
|
|
|
|
|
|
|
|
|
| Satellitenassoziationen bei autosomalen und gonosomalen Chromosomenanomalien und bei Hypothyreosen |
|
|
|
|
|
|
|
|
|
| Beitrag zur Genetik der Erythrocyten-Phosphoglucomutase |
|
|
|
|
|
|
|
|
|
| Zur formalen Genetik der Phosphoglucomutasen (EC: 2.7.5.1); Untersuchung von 366 Familien |
|
|
|
|
|
|
|
|
|
| Zur formalen Genetik der 6-Phosphogluconatdehydrogenasen (EC: 1.1.1.44); Untersuchung von 220 Familien |
|
|
|
|
|
|
|
|
|
| The HL-A transplantation system |
|
|
|
|
|
|
|
|
|
| Mewing cry in a child with the partial deletion of the short arm of chromosome No. 4 |
|
|
|
|
|
|
|
|
|
| Seasonal variation in non-disjunction of sex-chromosomes |
|
|
|
|
|
|
|
|
|