1.
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects
by Medina Gomez, Maria
American journal of human genetics, 2018, Vol.102 (1), p.88-102
2.
Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss
by Yariz, K.O
American journal of human genetics, 2012, Vol.91 (5), p.872-882
3.
Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa
by Angius, Andrea
American journal of human genetics, 2016-07-07, Vol.99 (1), p.236-245
4.
Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa
by Angius, Andrea
American journal of human genetics, 2018-04-05, Vol.102 (4), p.713-713
5.
Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa
by Angius, Andrea
American journal of human genetics, 2018-04-05, Vol.102 (4), p.713-713
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