Skip to content Skip to footer
214 Results for: "Genetics (clinical)"

Research output (156)

  1. Holt‐Oram syndrome in four half‐siblings with unaffected parents: brief clinical report

    Braulke, I., Herzog, S., Thies, U. & Zoll, B., Apr 1991, In: Clinical Genetics. 39, 4, p. 241-244 4 p.

    Research output: Contribution to journalResearch articleContributedpeer-review

    undefined
  2. The first mutation in CNGA2 in two brothers with anosmia

    Karstensen, H. G., Mang, Y., Fark, T., Hummel, T. & Tommerup, N., 1 Sept 2015, In: Clinical genetics. 88, 3, p. 293-296 4 p.

    Research output: Contribution to journalResearch articleContributedpeer-review

  3. Triple A syndrome: Genotype-phenotype assessment

    Prpic, I., Huebner, A., Persic, M., Handschug, K. & Pavletic, M., 1 May 2003, In: Clinical genetics. 63, 5, p. 415-417 3 p.

    Research output: Contribution to journalResearch articleContributedpeer-review

View all Research output

Journals (57)

  1. Clinical Genetics

    ISSNs: 0009-9163

    Additional searchable ISSN (electronic): 1399-0004

    Wiley-Blackwell, Oxford [u. a.]

    Scopus rating (2023): CiteScore 6.5 SJR 1.236 SNIP 1.245

    Journal

  2. Chromosoma

    ISSNs: 0009-5915

    Additional searchable ISSN (electronic): 1432-0886

    Springer Science and Business Media B.V.

    Scopus rating (2023): CiteScore 3.3 SJR 0.824 SNIP 0.485

    Journal

  3. BMC Genetics

    ISSNs: 1471-2156

    BioMed Central, London

    Scopus rating (2021): CiteScore 5.6 SJR 0.585 SNIP 1.126

    Indexed in DOAJ

    Journal

View all Journals

Activities (1)

  1. Clinical Genomic Sequencing in Oncology and Rare Diseases

    Schröck, E. (Speaker)
    23 May 2024

    Activity: Talk or presentation at external institutions/eventsTalk/PresentationInvited

View all Activities