Matches in DBpedia 2016-04 for { ?s ?p "Genetics Home Reference" }
- condition=leschnyhansyndrome author "Genetics Home Reference".
- elsi author "Genetics Home Reference".
- CHEK2 journal "Genetics Home Reference".
- 4c9abd25b318ad314834c0feb6649c43a71f4d99d32043e4e807c59581dda5a9 journal "Genetics Home Reference".
- e00b6ea8f3dd6e5050fc1557e72d204010e56fc3690eac276423e996042d2fa2 journal "Genetics Home Reference".
- weaver-syndrome last "Genetics Home Reference".
- GBE1 last "Genetics Home Reference".
- nbs last1 "Genetics Home Reference".
- 3-methylcrotonyl-coa-carboxylase-deficiency publisher "Genetics Home Reference".
- fukuyama-congenital-muscular-dystrophy publisher "Genetics Home Reference".
- glut1-deficiency-syndrome publisher "Genetics Home Reference".
- wnt4-mullerian-aplasia-and-ovarian-dysfunction publisher "Genetics Home Reference".
- condition=sandhoffdisease publisher "Genetics Home Reference".
- SLC2A1 publisher "Genetics Home Reference".
- MedlinePlus publisher "Genetics Home Reference".
- kabuki-syndrome publisher "Genetics Home Reference".
- lafora-progressive-myoclonus-epilepsy publisher "Genetics Home Reference".
- myoclonic-epilepsy-with-ragged-red-fibers publisher "Genetics Home Reference".
- ochoa-syndrome publisher "Genetics Home Reference".
- unverricht-lundborg-disease publisher "Genetics Home Reference".
- vacterl-association publisher "Genetics Home Reference".
- condition=prolidase-deficiency publisher "Genetics Home Reference".
- CPOX publisher "Genetics Home Reference".
- PEPD publisher "Genetics Home Reference".
- glossary=microdeletionsyndrome publisher "Genetics Home Reference".
- ghr.nlm.nih.gov title "Genetics Home Reference".
- lactose-intolerance title "Genetics Home Reference".
- MTHFR title "Genetics Home Reference".
- snp title "Genetics Home Reference".
- 4ddfa4f12937000c902050388fc4ab269e21e0325d1bce11db30b35726896072 title "Genetics Home Reference".
- Related+Gene(s) title "Genetics Home Reference".
- werner-syndrome title "Genetics Home Reference".
- BMP4 title "Genetics Home Reference".
- aceruloplasminemia website "Genetics Home Reference".
- alpha-thalassemia website "Genetics Home Reference".
- boomerang-dysplasia website "Genetics Home Reference".
- congenital-dyserythropoietic-anemia website "Genetics Home Reference".
- ehlers-danlos-syndrome website "Genetics Home Reference".
- lactose-intolerance website "Genetics Home Reference".
- leigh-syndrome website "Genetics Home Reference".
- tietz-syndrome website "Genetics Home Reference".
- CDKN2A website "Genetics Home Reference".
- description website "Genetics Home Reference".
- lactate-dehydrogenase-deficiency website "Genetics Home Reference".
- LDHB website "Genetics Home Reference".
- PANK2 website "Genetics Home Reference".
- 7ed33b1a100d0672e33c9bc4cc3737bff8cfffcf6af2546fba35d2a58895966a website "Genetics Home Reference".
- 15 website "Genetics Home Reference".
- 22q112-deletion-syndrome website "Genetics Home Reference".
- acatalasemia website "Genetics Home Reference".
- alstrom-syndrome website "Genetics Home Reference".
- baller-gerold-syndrome website "Genetics Home Reference".
- beta-thalassemia website "Genetics Home Reference".
- bloom-syndrome website "Genetics Home Reference".
- branchiootorenal-syndrome website "Genetics Home Reference".
- common-variable-immune-deficiency website "Genetics Home Reference".
- congenital-afibrinogenemia website "Genetics Home Reference".
- congenital-central-hypoventilation-syndrome website "Genetics Home Reference".
- dihydropyrimidine-dehydrogenase-deficiency website "Genetics Home Reference".
- frasier-syndrome website "Genetics Home Reference".
- gilbert-syndrome website "Genetics Home Reference".
- glucose-6-phosphate-dehydrogenase-deficiency website "Genetics Home Reference".
- glycogen-storage-disease-type-vii website "Genetics Home Reference".
- hereditary-paraganglioma-pheochromocytoma website "Genetics Home Reference".
- hystrix-like-ichthyosis-with-deafness website "Genetics Home Reference".
- lymphangioleiomyomatosis website "Genetics Home Reference".
- mccune-albright-syndrome website "Genetics Home Reference".
- methylmalonic-acidemia website "Genetics Home Reference".
- myasthenia-gravis website "Genetics Home Reference".
- nephronophthisis website "Genetics Home Reference".
- neurofibromatosis-type-1 website "Genetics Home Reference".
- neurofibromatosis-type-2 website "Genetics Home Reference".
- oculopharyngeal-muscular-dystrophy website "Genetics Home Reference".
- poland-syndrome website "Genetics Home Reference".
- polycystic-kidney-disease website "Genetics Home Reference".
- pulmonary-arterial-hypertension website "Genetics Home Reference".
- pulmonary-veno-occlusive-disease website "Genetics Home Reference".
- pyruvate-kinase-deficiency website "Genetics Home Reference".
- retinitis-pigmentosa website "Genetics Home Reference".
- tangier-disease website "Genetics Home Reference".
- transthyretin-amyloidosis website "Genetics Home Reference".
- uv-sensitive-syndrome website "Genetics Home Reference".
- waardenburg-syndrome website "Genetics Home Reference".
- ATP7A website "Genetics Home Reference".
- COX6B1 website "Genetics Home Reference".
- HDAC8 website "Genetics Home Reference".
- MMP2 website "Genetics Home Reference".
- MT-ND5 website "Genetics Home Reference".
- PABPN1 website "Genetics Home Reference".
- RELN website "Genetics Home Reference".
- RMRP website "Genetics Home Reference".
- SDHC website "Genetics Home Reference".
- SDHD website "Genetics Home Reference".
- WT1 website "Genetics Home Reference".
- gene=MT-ND6 website "Genetics Home Reference".
- glossary=hemihyperplasia website "Genetics Home Reference".
- glossary=somaticmutation website "Genetics Home Reference".
- glossary=translocation website "Genetics Home Reference".
- possiblemutations website "Genetics Home Reference".
- nbs website "Genetics Home Reference".