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Humangenetik

Humangenetik is a scientific journal, published since 1964 in English, French and German. The journal's country of origin is Germany and its primary focus area is genetics.
Details
Abbr. Humangenetik
Start 1964
End 1975
Frequency Irregular
p-ISSN 0018-7348
Country Germany
Languages English
French
German
Specialty Genetics
Recent Articles
1.
DNA replication patterns of human C group chromosomes from fibroblasts and amniotic fluid cells revealed by a Giemsa staining technique
Epplen J, Vogel W
Humangenetik . 1975 Dec; 30(4):337-9. PMID: 1240862
No abstract available.
2.
Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas
Zankl H, Weiss A, Zang K
Humangenetik . 1975 Dec; 30(4):343-8. PMID: 1218864
The recently detected reciprocal translocations in chronic myeloic leucemia (CML) and Burkitt's lymphoma (BL) made it necessary to clarify if meningiomas really show the described monosomy 22 or also a...
3.
Climate associated variations in the human serum albumin level
Walter H, Schobel B
Humangenetik . 1975 Dec; 30(4):331-5. PMID: 1218863
Quantitative determinations of the human serum albumin level showed significantly higher values in tropical (Negroes 46.98 mg/ml, Indians 54.30 mg/ml) than in non-tropical populations (Germans 44.41 mg/ml). These observations are...
4.
A technique for in situ karyotyping of primary amniotic fluid cell cultures
Schmid W
Humangenetik . 1975 Dec; 30(4):325-30. PMID: 1218862
A time proven technique is described for growing amniotic fluid cell cultures on cover glasses in Leighton tubes and for processing the mitotic cells in situ. Karyotyping the clones in...
5.
Sister chromatid exchanges and chromatid interchanges in bloom's syndrome
SCHROEDER T
Humangenetik . 1975 Dec; 30(4):317-23. PMID: 1218861
A comparison is made between the incidences of sister chromatid exchanges (SCE) per chromosome and group of chromosomes and breakage, visible at metaphase like open gaps, breaks, and breaks involved...
6.
Trisomy 9p due to paternal translocation, t(9;13) (q13;q12)
Schinzel A, Hayashi K, Schmid W
Humangenetik . 1975 Dec; 30(4):307-16. PMID: 1218860
A 16-year-old girl with trisomy 9p is described. She had a short stature, severe mental retardation and the following abnormal clinical findings: peculiar face with hypertelorism, downward slanting palpebral fissures,...
7.
The Bf locus in the HLA region of chromosome 6: linkage and association studies
Olaisen B, Teisberg P, Gedde-Dahl T, Thorsby E
Humangenetik . 1975 Dec; 30(4):291-6. PMID: 1218859
Bf allele frequencies in a material of 172 unrelated Norwegians are given. Bf/HLA linkage relations in 49 informative matings with 178 children, and Bf/HLA association data of a material of...
8.
A subtelocentric chromosome 9 in a dysplastic 18-year-old boy with dissociated mental development
Hansmann I, KEUTEL J
Humangenetik . 1975 Dec; 30(4):287-9. PMID: 1218858
A subtelocentric C-group chromosome was identified as inv(9) (p24q12) in an 18-year-old young man who shows few dysplastic signs and who suffers from dissociated mental development. Pericentric inversions producing an...
9.
Frequency of inborn errors of metabolism, especially PKU, in some representative newborn screening centers around the world: a collaborative study
Humangenetik . 1975 Dec; 30(4):273-86. PMID: 1218857
No abstract available.
10.
Contribution to the genetics of serum beta-lipoproteins in man. VIII. Linkage of the Ag h/i locus with the Ag x/y, Ag a1/d, Ag c/g, and Ag t/z loci
Morganti G, Beolchini P, Butler R, Vierucci A
Humangenetik . 1975 Dec; 30(4):341-2. PMID: 176106
No abstract available.