| On the Y fluorescence in human male fibroblasts |
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| Comments on the determination of isoenzyme polymorphism (ADA, AK, 6-PGD, PGM) by cellulose acetate electrophoresis |
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| Association between C′3 phenotypes and various diseases |
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| Sialic acid in erythrocytes of patients with amaurotic idiocy and Huntington's chorea |
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| Neues zur Genetik und Klassifikation der Muskeldystrophien |
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| Phenylbutazone, chloramphenicol and mammalian chromosomes |
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| Polymorphism of mitochondrial glutamic oxalo-acetic transaminase in a German population |
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| Age-related variation in the number of secondary associations between acrocentric chromosomes in normal females and patients with Turner's syndrome |
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| Follow-up of a family group suffering from ichthyosis hystrix type Curth-Macklin |
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| Population genetics of red cell galactose-1-phosphate-uridyl-transferase (EC: 2.7.7.12) |
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| A new rapid migrating variant in the Gc-system: Gc Wien |
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| Family studies on the third component of complement (C3), 6h1-antitrypsin polymorphism (locus E1 and E2) in the area of Marburg (Germany) |
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| Simplified methods for the measurement and electrophoretic demonstration of hypoxanthine-guanine phosphoribosyl transferase |
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| Observations in human spermatozoa by fluorescent “Acranil” staining |
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| Beobachtungen einer Familie mit Galaktos�mie und ?Duarte-Variante? |
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| The correspondence between quinacrine banding patterns and sites of secondary constrictions in human chromosomes |
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| Contribution to the genetics of serum ?-lipoprotein in man |
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| Adenosine deaminase (ADA) polymorphism in Northern England |
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| Incidence of cardiac malformations in Greenlandic Eskimos |
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✓ |
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Greenlandic Eskimos |
| Dominant inheritance of absence of the breast |
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| Giemsa banding in the D1 trisomy syndrome |
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| Partial monosomies 18 |
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| A newborn with the cat-eye syndrome |
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| Identification of two Robertsonian translocations with a Giemsa banding technique |
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| Ultrastructural distinction of autosomal dominant ichthyosis vulgaris and X-linked recessive ichthyosis |
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| Trisomy 14 in spontaneous abortus |
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| The phosphoglucomutase (PGM1)-groups in the Swiss population |
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| ?Relatedness? between antibodies ?Implications on immunogenetic systems |
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| Serogenetic investigations on malignant melanomas with reference to the incidence of AB0 system, Rh system, Gm, Inv, Hp and Gc systems |
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| Geometric fitness coefficients and inbreeding |
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| Identification of individual chromosomes in the human karyotype by their banding pattern after proteolytic digestion |
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| GPT, 6-PGD, PGM and AK phenotyping inone starch gel |
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| A further case of basal cell nevus syndrome and structural chromosome abnormalities |
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| Autosomal dominante Vererbung von Gaumenspalte und Synechien zwischen Gaumen und Mundboden oder Zunge |
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| A simple banding technique for identification of human metaphase chromosomes |
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| Further studies on the AB0-typing of ancient bones |
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| Chromosomenanalysen nach Ultraschalleinwirkung |
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| Evidence of the absence of Y fluorescent material in XX men |
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| Identification of G-group chromosomes involved in a G/G tandem-translocation by the Giemsa-band technique |
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| The biological significance of the histocompatibility antigens |
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| Geographic and ethnic distribution of some red cell enzymes |
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| Horizontal polyacrylamide electrophoresis for the determination of serum protein (haptoglobin) and red cell enzyme polymorphisms |
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| Some notes on the geographical distribution of the human red cell acid phosphatase phenotypes |
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| New data on the association between PTC and thyroid diseases |
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| Untersuchung �ber die H�ufigkeiten angeborener Stoffwechselanomalien in Ost- und West-�sterreich |
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| Cat-eye syndrome, a partial trisomy 22 |
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| Chromosome analysis of a primary carcinoma of the Fallopian tube |
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| Polymorphismus der erythrocyt�ren NADH-Diaphorase in der westdeutschen Bev�lkerung |
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✓ |
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westdeutschen Bevölkerung |
| 1st der von F. Lenz beschriebene typus der Farbensinnst�rung wirklich eine neue Variet�t des Farbensinns? |
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| Syndrome de Lesch-Nyhan |
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| Partielle Trisomie des kurzen Arms von Chromosom 4 mit Translokation 4p-,18q+ beim Vater |
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| Meine Antwort auf W. Jaegers brief an die herausgeber |
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| Inherited high serum levels of a functionally deficient complement esterase inhibitor associated with Hereditary Angioedema |
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| Further studies on the distribution of some serum protein and enzyme groups in South India |
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| Red cell enzyme polymorphisms in Bulgaria |
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| A marker chromosome number 14 with double satellite observed in two generations: An unbalanced chromosome constitution associated with normal phenotype |
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| Gene activation during early development of mammals |
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| Untersuchungen zum C?3-Polymorphismus (? 1c-Globulin) |
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| Familial translocation t(3q+;8q?) studied by banding with Giemsa staining |
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| Chromosomenuntersuchungen bei akuter virushepatitis |
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| Neuer Typ einer recessiv X-chromosomal vererbten Muskeldystrophie: Scapulo-humero-distale Muskeldystrophie mit fr�hzeitigen Kontrakturen und Herzrhythmusst�rungen |
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| Hereditary angioedema |
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| Dicentric and monocentric Robertsonian translocations in man |
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| Genetic studies on southeastern Bantu of Mozambique |
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| Studies on the Australia antigen |
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| Studies on the Australia antigen |
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| Simple smear method for the sampling and culturing of embryonal and fetal tissues |
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| Paternal transmission of a B/D translocation, t(4p-; 14p+ or 15p+), resulting in a partial 4p trisomy |
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| Identification and location of the Y-body in interphase by quinacrine and Giemsa |
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| Monosomy 21 in spontaneous abortus |
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| Chromosomenuntersuchungen bei behandlung mit Anticonvulsiva |
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| Nucleoli and chromosomes: Their relationships during the meiotic prophase of the human fetal oocyte |
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| Contribution to the AK and 6-PGD polymorphism in prague |
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| A modified method of culturing human amniotic fluid cells for prenatal detection of genetic disorders |
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| Defective decarboxylase in branched chain ketoacid oxidase multienzyme complex in classic type of maple syrup urine disease |
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| Gonadendysgenesie mit ungew�hnlicher Strukturanomalie eines X-Chromosoms (45,X/46,XXq+) |
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| C 11/D 13-translocation in four generations |
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| The lymphocyte as a dosimeter: Comparison of somatic chromosome aberrations in 522 newborn infants and 602 mothers |
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| New families, onw with two recombinants for estimation of recombination between the Deutan and protan loci |
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| Hp, Gc, Cp, Tf, Bg and Pi phenotypes in leprosy patients and healthy controls from West Bengal (India) |
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| Constitutive heterochromatin patterns of G-group chromosomes in Down's syndrome |
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| Polymorphism of erythrocyte phosphoglucomutase, adenylate kinase and adenosine deaminase in northern Thailand |
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| 4th Annual Meeting of the ?Gesellschaft f�r Genetik? |
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| Parent-child relationship and sex differences in skin tanning potential in man |
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| Ring-chromosom 18 |
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| XXXY Klinefelter-Syndrom |
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| Effect of different serologic transformations of T5 universes |
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| A propos de la dysplasie des cr�tes �pidermiques |
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| Quinacrine fluorescence patterns in somatic chromosomes of a t(15q15q) carrier |
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| �ber rudiment�re Polydaktylie bei Bantu-Negern |
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✓ |
|
Bantu-Negern |
| Gleichzeitige Auftrennung von AK- und ADA-Isoenzymen auf einer Folie |
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| Glucose-6-phosphate dehydrogenase deficiency and colour-vision studies in Indian Muslims |
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| Different chromosome variants of Klinefelter's syndrome and plasma testosterone |
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| A phenotypic male with karyotype 45,X/45,X,ace+(?Yq-) |
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| Phenotype frequencies for four serum proteins in Afghanistan: Two ?new? albumin variants |
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| A rapid banding technique for routine use in human and comparative cytogenetics |
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| Lactate dehydrogenase isoenzymes in oocytes and unfertilized eggs of mammals |
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| 46,XY/47,XY, 18+ Mosaicism with a 23-year survival |
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| Genetic linkage relationships of the ADA and 6-PGD loci in ?Humangenetik? |
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| Alpha1-antitrypsin levels and electrophoretic patterns of several deficient phenotypes |
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| Beitrag zum Bloom-Syndrom |
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| Short arm deletion of chromosome 14 |
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| Ein klassisches Bogenmuster auf der Palma des Menschen, ein vermutlich einmaliges Vorkommen |
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| Erfahrungen mit einer bisher verkannten Variet�t des Farbensinns und Folgen f�r Theorie und Praxis |
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| Unusual findings by fluorescence microscopy of a t(13q14q) |
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| Further observations on a previously reported case of 4p-syndrome |
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| On the population genetics of the ceruloplasmin polymorphism |
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| The rare ?silent? allele PO or PV (PVienna) of human red cell acid phosphatase, typed in a second family |
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| Famili�rer Minderwuchs mit unproportioniert hohen Wirbeln |
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| Histologische Analysen von triploiden Spontanaborten |
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| C trisomy in bone marrow cells in a case of pre-leukaemic acute myelogenous leukaemia |
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| Localization of the deleted segment in the cri-du-chat syndrome |
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| A case of the 18p?Syndrome |
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| Bloom's syndrome |
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| Lipoproteins in LCAT-deficiency |
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| Chromosome studies in patients with ulcerative colitis |
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| Mit einem alkylierenden Agens (Zitostop) in vitro induzierbare Mutationen bei Malignomen und bei Syndromen, die zur Malignit�t disponieren |
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| Measurement of human ribosomal DNA in relation to a possible deficiency |
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| Homozygous duplication on long arm of chromosome pair no. 1 |
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| Zur frage der unterschiedlichen Verteilung der ABO-Blutgruppen bei erst-und nachgeborenen Kindern |
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| Red blood cell NADH diaphorase in Italian populations |
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✓ |
|
Italian populations |
| Zum Polymorphismus der Glutamat-Pyruvat-Transaminase (GPT) menschlicher Erythrocyten in Westdeutschland |
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| Gene frequencies of soluble glutamic-pyruvic-transaminase in a northern German population (Hamburg) |
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| Contribution to the genetics of serum ?-lipoprotein in man |
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