Hutchinson–Gilford progeria syndrome
NJ Ullrich, LB Gordon - Handbook of clinical neurology, 2015 - Elsevier
Hutchinson–Gilford progeria syndrome (HGPS) is an extremely rare, uniformly fatal,
segmental “premature aging” disease in which children exhibit phenotypes that may give us …
segmental “premature aging” disease in which children exhibit phenotypes that may give us …
Hutchinson-Gilford progeria syndrome.
NJ Ullrich, LB Gordon - Handbook of Clinical Neurology, 2015 - europepmc.org
Hutchinson-Gilford progeria syndrome (HGPS) is an extremely rare, uniformly fatal,
segmental" premature aging" disease in which children exhibit phenotypes that may give us …
segmental" premature aging" disease in which children exhibit phenotypes that may give us …
Hutchinson–Gilford progeria syndrome
NJ ULLRICH, LB GORDON - Neurocutaneous Syndromes, 2015 - books.google.com
Hutchinson–Gilford progeria syndrome (HGPS) is an autosomal dominant, rare, fatal
pediatric segmental premature aging disease (Gordon et al., 2003). The first description of …
pediatric segmental premature aging disease (Gordon et al., 2003). The first description of …
[引用][C] Hutchinson–Gilford progeria syndrome
NJ Ullrich, LB Gordon - Neurocutaneous Syndromes, 2015 - cir.nii.ac.jp
Hutchinson-Gilford progeria syndrome
NJ Ullrich, LB Gordon - Handbook of clinical neurology, 2015 - pubmed.ncbi.nlm.nih.gov
Hutchinson-Gilford progeria syndrome (HGPS) is an extremely rare, uniformly fatal,
segmental" premature aging" disease in which children exhibit phenotypes that may give us …
segmental" premature aging" disease in which children exhibit phenotypes that may give us …