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Human Genetics - 1971
95 articles | Last updated: 2025-12-03 14:12:56
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Partial XYY syndrome
Etude d'une observation de chromosome du groupe 13?15 en anneau (46,XY,15r)
Zur transspezifischen Variabilit�t der Glucose-6-Phosphatdehydrogenase (E.C.: 1.1.1.49) der Primaten
Evidence for linkage between the locus for the AB0-system and the locus for phosphoglucoseisomerase (PGI)
Zur transspezifischen Variabilit�t der 6-Phosphogluconatdehydrogenase (E.C.: 1.1.1.44) der Primaten
Zur transspezifischen Variabilit�t der NAD-Malatdehydrogenase (E.C.: 1.1.1.37) der Primaten
Erythrocytenenzyme der Primaten
On the non-random involvement of D-group chromosomes in centric fusion translocations in man
Alpha1-antitrypsin: Physiology, genetics and pathology
Possible linkage between uncoiler chromosome Un 1 and mylase polymorphism Amy 2 loci
Studies of enzymes connected with erythrocyte glutathione metabolism in a rural tropical population
Dysplasie des cr�tes �pidermiques, � h�r�dit� dominante autosomique
Ein sehr seltener Ph�notyp im Isoenzymsystem der Adenylatkinase des Menschen: AK 3-2
Die Wirkung von L-Cystein auf die Aberrationsausl�sung in menschlichen Chromosomen durch chemische Mutagene
69, XYY sporadic triploidy in an adult
Vergr��erte sekund�re Einschn�rung des Chromosoms C9 bei Mutter und Kind
Hereditary congenital coxa vara with dominant inheritance?
Heterogeneity of Chondrodysplasia punctata
Father and son with karyotype 47,XY,?Yq-
Cytological and cytogenetical studies on brain tumors
Cytogenetic investigation of spontaneous abortions
Presumed disturbance of a nucleolus organizer in man: Chromosome 13qs and monosomy 15 mosaicism
Erythrocytenenzyme der Primaten
Evaluation of a heterozygote test for maple syrup urine disease in leucocytes and cultured fibroblasts
Biochemische, histologische und klinische Befunde bei einer vierj�hrigen Konduktorin der gutartigen X-chromosomalen Muskeldystrophie (Typ Becker)
Ulcero-mutilating acropathy, hereditary sensory neuropathy and signs of friedreich heredo-ataxia in two brothers
Genetic and constitutional influences on serum-uric-acid in a tropical rural population
Zur transspezifischen Variabilit�t der NADH-Diaphorase der Primaten
AB0 blood groups, inv serum groups, and serum proteins in leprosy patients from West Bengal (India)
Untersuchungen zur armverh�ltnisbestimmung am sp�treplizierenden X-Chromosom des Menschen
Zur spezifischen Wirkung von Phenylbutazon auf die Mitose menschlicher Lymphocyten in vitro
Population study of erythrocyte glutathione reductase activity
Kurze mitteilungen
Inv phenotypes and quantitative gamma globulin determinations in leprosy patients and control populations from India and Thailand
Problematischer Mutter-Kind-Ausschlu� mit PGM1
Hp 2?2 like phenotypes in mammals
Fluorescence staining method for the morphological and structural study of human chromosomes
Polyploidisierung in der Fischfamilie Cyprinidae, Ordnung Cypriniformes
Eine humane serumalbuminvariante (Doppelalbumin�mie)
In vitro alteration of association patterns of human acrocentric chromosomes
Zur populationsgenetik der phosphoglucoseisomerase (EC: 5.3.1.9)
PGM 1 8 in two German families
45,XO Turner's syndrome, Wilm's tumor and imperforate anus
Incidence of abnormal haemoglobins in different ethnic groups of Indians
Induced chromosome aberrations in early embryogenesis of mice
Haemagglutination-inhibiting variola antibodies in blood serum of former smallpox patients, their healthy siblings, and unvaccinated controls from other areas
Down's syndrome
G�n�tique du syndrome d'Alport
Cytological and cytogenetical studies on brain tumors
A strongly fluorescing abnormal chromosome in a malformed child
Human chromosomes and fluorescence
Chemical mutagenesis the Chinese hamster bone marrow as an in vivo test system
Chemical mutagenesis the Chinese hamster bone marrow as an in vivo test system
Pr�natale Chromosomenanalyse mit Mosaikbefund 46,XX/92,XXXX
A balanced 13/18 translocation [46,XY,t(13q-; 18q+)] in the father of an infant with multiple anomalies
On intrauterine selection by AB0-incompatibility with special reference to maternal age
Two further males with female karyotypes
Unterschiedliche fluorescenz der beiden homologen chromosomen Nr. 3 beim menschen
Identification of G group anomalies in Down's syndrome by quinacrine dihydrochloride fluorescence staining
Chromosomenuntersuchungen bei Kindern von Imuran�-behandelten Eltern
Y-body in hair roots
Untersuchungen zur genetik des merkmals ?Fingerbehaarung?
Investigations on the geographical variability of the human transferrins
Population study of erythrocyte glutathione reductase activity
Studies on haptoglobin and transferrin types in Khatris and Aroras of Punjab, India
Double satellites: Autoradiographic study of a chromosomal marker observed in two generations
The identification of the chromosomes of the F group by quantitative methods, with an appendix on the relative DNA measurements of human chromosomes
Methodological investigations on the AB0-Typing of ancient bones
New biochemical and immunological data on quantitative and qualitative variability of human pseudocholinesterase
Adenylate kinase and malate dehydrogenase in four Malaysian racial groups
Transspecific variability of D-fructose-1,6-diphosphate-1-phosphohydrolase (E.C.: 3.1.3.11) in Primates
Stature and weight in boys with the XYY syndrome
Genetics and linkage analysis of adenosine deaminase
Indophenol oxydase variability
Population genetics of soluble glutamic-pyruvic transaminase (EC:2.6.1.2): Gene frequencies in Southwestern Germany
A simplified method of demonstrating Giemsa-Band pattern in human chromosomes
Adenosine deaminase polymorphism in sardinia
Studie zur intrachromosomalen Bruchverteilung bei menschlichen Leukocyten
Variations in karyotypes of normal premature babies, new-born babies and infants
Genetic and linkage analysis on 6-PGD
Phosphoglucomutase (PGM) and 6-phosphogluconate dehydrogenase (PGD) isozymes in human sperm cells
Waardenburg's syndrome in two siblings and their parents
Transspecific variability of phosphohexose isomerase (E. C.: 5. 3. 1. 9) in primates
Dicentric chromosome due to an unusual fusion
XXXXY syndrome in a phenotypic male infant with associated cardiac abnormalities
Pseudocholinesterase polymorphism among Lapp populations in Finland
Synchronous activation of the alleles coding for the S-form of the NADP-dependent malate dehydrogenase during mouse embryogenesis
The adnylate kinase (AK)-groups in the Swiss population
Beitrag zur Populationsgenetik der Adenosindesaminase
Analytical review: The pathogenesis of diabetes mellitus and its relationship to biological aging
Duplication deficiency syndrome in familial translocation (2q-; 5p+)
Adenylate kinase polymorphism in populations in Finland (Swedes, Finns, Lapps), in Maris, and in Greenland Eskimos
✓
Swedes, Finns, Lapps, Maris, Greenland Eskimos
Ring G-Chromosom
Weitere Untersuchungen des Hautleistensystems bei Thyreoiditis lymphomatosa Hashimoto
Fluorescence pattern of a dicentric Y