Research output (156)
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 journal › Research article › Contributed › peer-review
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 journal › Research article › Contributed › peer-review
PublishedTriple 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 journal › Research article › Contributed › peer-review
Published
Journals (57)
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
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
BMC Genetics
ISSNs: 1471-2156
BioMed Central, London
Scopus rating (2021): CiteScore 5.6 SJR 0.585 SNIP 1.126
Indexed in DOAJ
Journal
Activities (1)
Clinical Genomic Sequencing in Oncology and Rare Diseases
Schröck, E. (Speaker)23 May 2024Activity: Talk or presentation at external institutions/events › Talk/Presentation › Invited