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The European Journal of Medical Genetics is a monthly peer-reviewed medical journal covering medical genetics in human and experimental systems. It was established in 1958 as Annales de Génétique, obtaining its current name in 2005.
Journal of Medical Biochemistry: Biochemistry: Walter de Gruyter: English: 1982–present Journal of Medical Biography: Medical Personnel: SAGE Publishing: English: 1993–present Journal of Medical Case Reports: Medicine: BioMed Central: English: 2007–present Journal of Medical Economics: Medicine: Taylor and Francis Group: English: 1998 ...
The European Journal of Human Genetics is a monthly peer-reviewed scientific journal published by the Nature Publishing Group on behalf of the European Society of Human Genetics. It covers all aspects of human genetics .
This category is for scientific and medical journals covering the fields of human and medical genetics. Pages in category "Medical genetics journals" The following 24 pages are in this category, out of 24 total.
The European Society of Human Genetics (ESHG) is a non-profit organization that promotes research, facilitates communication and encourages best practice in applications of human and medical genetics, particularly in Europe. [1] The society organizes the annual European Human Genetics Conference and publishes the European Journal of Human ...
The Journal of Medical Genetics is a monthly peer-reviewed medical journal covering all aspects of medical genetics, including reviews of and opinion on the latest developments. It was established in 1964 and is published by the BMJ Group .
In another study published by the Journal of Medical Genetics, DNA from forty patients were extracted and subjected to MLPA, FISH or EHMT1 sequencing. The forty patients were divided into two groups: 1 group of 16 patients with the 9q34 deletion, and 1 group of 24 with typical FISH/MPLA results.
Nablus mask-like facial syndrome (Nablus syndrome) is a rare (13 cases described by 2018) genetic condition. [1] It is a microdeletion syndrome triggered by a deletion at chromosome 8 q22.1 that causes a mask-like facial appearance in those affected. [2]