Robert Hufnagel to Sequence Analysis, DNA
This is a "connection" page, showing publications Robert Hufnagel has written about Sequence Analysis, DNA.
Connection Strength
0.139
-
Using human sequencing to guide craniofacial research. Genesis. 2019 01; 57(1):e23259.
Score: 0.040
-
Clinical and molecular phenotyping of a child with Hermansky-Pudlak syndrome-7, an uncommon genetic type of HPS. Mol Genet Metab. 2017 04; 120(4):378-383.
Score: 0.036
-
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder. Nat Genet. 2015 Aug; 47(8):926-32.
Score: 0.032
-
Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopecia. Am J Hum Genet. 2015 Apr 02; 96(4):519-31.
Score: 0.031