Genetics in Medicine

Abkürzung der Fachzeitschrift: GENET MED
ISSN: 1098-3600
Verlag: Nature Publishing Group: Open Access Hybrid Model Option B



Publikationen


Heftnummer: 4, Band: 21, Seitenbereich: 1001-1007
Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot (2019)
Reuter MS, Jobling R, Chaturvedi RR, et al.


PEDIA: prioritization of exome data by image analysis (2019)
Hsieh TC, Mensah MA, Pantel JT, et al.


Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants (2018)
Johnston JJ, Van Der Smagt JJ, Rosenfeld JA, et al.

Heftnummer: 6, Band: 20, Seitenbereich: 630-638
Clinical relevance of systematic phenotyping and exome sequencing in patients with short stature (2018)
Hauer N, Popp B, Schoeller E, et al.

Heftnummer: 9, Band: 20, Seitenbereich: 965-975
Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care (2018)
Ivanovski I, Djuric O, Caraffi SG, et al.

Heftnummer: 5, Band: 19, Seitenbereich: 599-603
Genetic modifiers of CHEK2*1100delC-associated breast cancer risk (2017)
Muranen TA, Greco D, Blomqvist C, et al.

Band: 17, Seitenbereich: 765-773
Economic evaluation of genetic screening for Lynch syndrome in Germany (2015)
Severin F, Stollenwerk B, Holinski-Feder E, et al.


Zuletzt aktualisiert 2015-29-05 um 16:47