Hummel K - Search Results

1

Plasminogen hemizygosity. Detection of a silent allele in 7 members of a family by determination of plasminogen phenotypes, antigenic levels, and functional activity.

Skoda U, Goldmann SF, Händler C, Hummel K, Lechler E, Lübcke I, Mauff G, Meyer-Börnecke D, Pesch S, Pulverer G. Skoda U, et al. Among authors: hummel k. Vox Sang. 1988;54(4):210-4. doi: 10.1111/j.1423-0410.1988.tb03907.x. Vox Sang. 1988. PMID: 3388818

2

Proposal for the nomenclature of human plasminogen (PLG) polymorphism.

Skoda U, Bertrams J, Dykes D, Eiberg H, Hobart M, Hummel K, Kühnl P, Mauff G, Nakamura S, Nishimukai H, et al. Skoda U, et al. Among authors: hummel k. Vox Sang. 1986;51(3):244-8. doi: 10.1111/j.1423-0410.1986.tb01963.x. Vox Sang. 1986. PMID: 3811320

3

Inheritance of cis-AB in three generations (family Lam.).

Hummel K, Badet J, Bauermeister W, Bender K, Duffner G, Lopez M, Mauff G, Pulverer G, Salmon C, Schmidts W. Hummel K, et al. Vox Sang. 1977;33(5):290-8. doi: 10.1111/j.1423-0410.1977.tb04478.x. Vox Sang. 1977. PMID: 919419

4

Properdin factor B (glycine-rich beta-glycoprotein or C3 proactivator)-polymorphism: genetic and biochemical aspects. First application to paternity cases.

Mauff G, Hummel K, Pulverer G. Mauff G, et al. Among authors: hummel k. Z Immunitatsforsch Exp Klin Immunol. 1975 Oct;150(4):327-38. Z Immunitatsforsch Exp Klin Immunol. 1975. PMID: 129976

5

Occurrence of Su in a German family.

Mauff G, Pulverer G, Hummel K, Spielmann W, Bender K. Mauff G, et al. Among authors: hummel k. Blut. 1977 May;34(5):357-62. doi: 10.1007/BF00996075. Blut. 1977. PMID: 871535

6

[Blood group opinion and judicial judgement 1. 250 paternity cases 1965-1970 (author's transl)].

Hellenbroich H, Hummel K, Pulverer G. Hellenbroich H, et al. Among authors: hummel k. Z Immunitatsforsch Exp Klin Immunol. 1975 Jul;149(5):456-62. Z Immunitatsforsch Exp Klin Immunol. 1975. PMID: 126577 German.

7

[Distribution of types of erythrocyte acid phosphatases in the German population].

Pulverer G, Hummel K, Weidtman V. Pulverer G, et al. Among authors: hummel k. Z Immunitatsforsch Allerg Klin Immunol. 1969 Nov;138(5):475-9. Z Immunitatsforsch Allerg Klin Immunol. 1969. PMID: 4244399 German. No abstract available.

8

[Phenotype frequencies in the genetic systems haptoglobin, Gc, erythrocyte acid phosphatase, phosphoglucomutase and adenylate kinase, as well as the genetic properties Gm(1), Gm(2) and Inv(1) in German population (Freiburg i Br and Cologne) and in Turkish people].

Hummel K, Pulverer G, Schaal KP, Weidtman V. Hummel K, et al. Humangenetik. 1970;8(4):330-3. doi: 10.1007/BF00280333. Humangenetik. 1970. PMID: 5436703 German. No abstract available.

9

New mutation versus exclusion at the alpha-1-antitrypsin locus: a multifaceted approach in a problematical paternity case.

Bender K, Kasulke D, Mayerovà A, Hummel K, Weidinger S, Epplen JT, Wienker TF. Bender K, et al. Among authors: hummel k. Hum Hered. 1991;41(1):1-11. doi: 10.1159/000153966. Hum Hered. 1991. PMID: 2050377

10

New mutation to Huntington's disease.

Wolff G, Deuschl G, Wienker TF, Hummel K, Bender K, Lücking CH, Schumacher M, Hammer J, Oepen G. Wolff G, et al. Among authors: hummel k. J Med Genet. 1989 Jan;26(1):18-27. doi: 10.1136/jmg.26.1.18. J Med Genet. 1989. PMID: 2563774 Free PMC article.

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