[PDF][PDF] De novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea
Clinical whole-exome sequencing (WES) for identification of mutations leading to Mendelian
disease has been offered to the medical community since 2011. Clinically undiagnosed …
disease has been offered to the medical community since 2011. Clinically undiagnosed …
De novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea.
F Xia, MN Bainbridge, TY Tan, MF Wangler… - American Journal of …, 2014 - europepmc.org
Clinical whole-exome sequencing (WES) for identification of mutations leading to Mendelian
disease has been offered to the medical community since 2011. Clinically undiagnosed …
disease has been offered to the medical community since 2011. Clinically undiagnosed …
De novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea
F Xia, MN Bainbridge, TY Tan… - … journal of human …, 2014 - pubmed.ncbi.nlm.nih.gov
Clinical whole-exome sequencing (WES) for identification of mutations leading to Mendelian
disease has been offered to the medical community since 2011. Clinically undiagnosed …
disease has been offered to the medical community since 2011. Clinically undiagnosed …
[HTML][HTML] De Novo Truncating Mutations in AHDC1 in Individuals with Syndromic Expressive Language Delay, Hypotonia, and Sleep Apnea
F Xia, MN Bainbridge, TY Tan, MF Wangler… - The American Journal of …, 2014 - Elsevier
Clinical whole-exome sequencing (WES) for identification of mutations leading to Mendelian
disease has been offered to the medical community since 2011. Clinically undiagnosed …
disease has been offered to the medical community since 2011. Clinically undiagnosed …
De Novo Truncating Mutations in AHDC1 in Individuals with Syndromic Expressive Language Delay, Hypotonia, and Sleep Apnea
F Xia, MN Bainbridge, TY Tan, MF Wangler… - The American Journal of …, 2014 - infona.pl
Clinical whole-exome sequencing (WES) for identification of mutations leading to Mendelian
disease has been offered to the medical community since 2011. Clinically undiagnosed …
disease has been offered to the medical community since 2011. Clinically undiagnosed …
De novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea
F Xia, MN Bainbridge, TY Tan… - American …, 2014 - utsouthwestern.elsevierpure.com
Clinical whole-exome sequencing (WES) for identification of mutations leading to Mendelian
disease has been offered to the medical community since 2011. Clinically undiagnosed …
disease has been offered to the medical community since 2011. Clinically undiagnosed …
[引用][C] De Novo Truncating Mutations in AHDC1 in Individuals with Syndromic Expressive Language Delay, Hypotonia, and Sleep Apnea
F Xia, MN Bainbridge, TY Tan, MF Wangler… - The American Journal …, 2014 - cir.nii.ac.jp
De Novo Truncating Mutations in AHDC1 in Individuals with Syndromic Expressive Language
Delay, Hypotonia, and Sleep Apnea | CiNii Research CiNii 国立情報学研究所 学術情報 …
Delay, Hypotonia, and Sleep Apnea | CiNii Research CiNii 国立情報学研究所 学術情報 …
[HTML][HTML] De Novo Truncating Mutations in AHDC1 in Individuals with Syndromic Expressive Language Delay, Hypotonia, and Sleep Apnea
F Xia, MN Bainbridge, TY Tan, MF Wangler… - American Journal of …, 2014 - ncbi.nlm.nih.gov
Clinical whole-exome sequencing (WES) for identification of mutations leading to Mendelian
disease has been offered to the medical community since 2011. Clinically undiagnosed …
disease has been offered to the medical community since 2011. Clinically undiagnosed …
De novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea.
F Xia, MN Bainbridge, TY Tan, MF Wangler… - American Journal of …, 2014 - europepmc.org
Clinical whole-exome sequencing (WES) for identification of mutations leading to Mendelian
disease has been offered to the medical community since 2011. Clinically undiagnosed …
disease has been offered to the medical community since 2011. Clinically undiagnosed …