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HGG Advances
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April 26, 2022
Variants in <i>PHF8</i> cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology
Andrew K Sobering, Laura M Bryant, Dong Li, et al.
HGG Advances
|
December 30, 2022
Erratum: Variants in <i>PHF8</i> cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology
Andrew K Sobering, Laura M Bryant, Dong Li, et al.
American Journal of Medical Genetics. Part A
|
March 30, 2021
Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner syndrome
Sarah E Sheppard, Ian M Campbell, Margaret H Harr, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 23) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 23 results.
HGG Advances
|
April 26, 2022
Variants in <i>PHF8</i> cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology
Andrew K Sobering, Laura M Bryant, Dong Li, et al.
HGG Advances
|
December 30, 2022
Erratum: Variants in <i>PHF8</i> cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology
Andrew K Sobering, Laura M Bryant, Dong Li, et al.
American Journal of Medical Genetics. Part A
|
March 30, 2021
Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner syndrome
Sarah E Sheppard, Ian M Campbell, Margaret H Harr, et al.
Page
of 3