[HTML] springer.comFull View

[HTML][HTML] Molecular genetic characterization of cblC defects in 126 pedigrees and prenatal genetic diagnosis of pedigrees with combined methylmalonic aciduria and …

S Hu, S Mei, N Liu, X Kong - BMC medical genetics, 2018 - Springer
Background We sought to analyse MMACHC variants among 126 pedigrees with cobalamin
(cbl) C deficiency and combined methylmalonic aciduria and homocystinuria by Sanger …
被引用次数：37 相关文章
[HTML] biomedcentral.com

[HTML][HTML] Molecular genetic characterization of cblC defects in 126 pedigrees and prenatal genetic diagnosis of pedigrees with combined methylmalonic aciduria and …

S Hu, S Mei, N Liu, X Kong - BMC Medical …, 2018 - bmcmedgenet.biomedcentral.com
We sought to analyse MMACHC variants among 126 pedigrees with cobalamin (cbl) C
deficiency and combined methylmalonic aciduria and homocystinuria by Sanger …
[PDF] archive.org

[PDF][PDF] Molecular genetic characterization of cblC defects in 126 pedigrees and prenatal genetic diagnosis of pedigrees with combined methylmalonic aciduria and …

S Hu, S Mei, N Liu, X Kong - 2018 - scholar.archive.org
Background: We sought to analyse MMACHC variants among 126 pedigrees with
cobalamin (cbl) C deficiency and combined methylmalonic aciduria and homocystinuria by …

Molecular genetic characterization of cblC defects in 126 pedigrees and prenatal genetic diagnosis of pedigrees with combined methylmalonic aciduria and …

S Hu, S Mei, N Liu, X Kong - BMC Medical Genetics, 2018 - europepmc.org
Background We sought to analyse MMACHC variants among 126 pedigrees with cobalamin
(cbl) C deficiency and combined methylmalonic aciduria and homocystinuria by Sanger …

Molecular genetic characterization of cblC defects in 126 pedigrees and prenatal genetic diagnosis of pedigrees with combined methylmalonic aciduria and …

S Hu, S Mei, N Liu, X Kong - BMC Medical Genetics, 2018 - search.ebscohost.com
Background: We sought to analyse MMACHC variants among 126 pedigrees with
cobalamin (cbl) C deficiency and combined methylmalonic aciduria and homocystinuria by …

Molecular genetic characterization of cblC defects in 126 pedigrees and prenatal genetic diagnosis of pedigrees with combined methylmalonic aciduria and …

S Hu, S Mei, N Liu, X Kong - BMC medical genetics, 2018 - pubmed.ncbi.nlm.nih.gov
Background We sought to analyse MMACHC variants among 126 pedigrees with cobalamin
(cbl) C deficiency and combined methylmalonic aciduria and homocystinuria by Sanger …

Molecular genetic characterization of cblC defects in 126 pedigrees and prenatal genetic diagnosis of pedigrees with combined methylmalonic aciduria and …

S Hu, S Mei, N Liu, X Kong - BMC Medical Genetics, 2018 - search.proquest.com
Background We sought to analyse MMACHC variants among 126 pedigrees with cobalamin
(cbl) C deficiency and combined methylmalonic aciduria and homocystinuria by Sanger …
[HTML] nih.gov

[HTML][HTML] Molecular genetic characterization of cblC defects in 126 pedigrees and prenatal genetic diagnosis of pedigrees with combined methylmalonic aciduria and …

S Hu, S Mei, N Liu, X Kong - BMC Medical Genetics, 2018 - ncbi.nlm.nih.gov
Background We sought to analyse MMACHC variants among 126 pedigrees with cobalamin
(cbl) C deficiency and combined methylmalonic aciduria and homocystinuria by Sanger …
[PDF] biomedcentral.com

[PDF][PDF] Molecular genetic characterization of cblC defects in 126 pedigrees and prenatal genetic diagnosis of pedigrees with combined methylmalonic aciduria and …

S Hu, S Mei, N Liu, X Kong - 2018 - bmcmedgenet.biomedcentral.com
Background: We sought to analyse MMACHC variants among 126 pedigrees with
cobalamin (cbl) C deficiency and combined methylmalonic aciduria and homocystinuria by …