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American Journal of Medical Genetics. Part A
|
December 23, 2011
Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay
Eric A Muller, Swaroop Aradhya, Joan F Atkin, et al.
American Journal of Human Genetics
|
July 22, 2020
De Novo Variants in the ATPase Module of MORC2 Cause a Neurodevelopmental Disorder with Growth Retardation and Variable Craniofacial Dysmorphism
Maria J Guillen Sacoto, Iva A Tchasovnikarova, Erin Torti, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 11, 2023
Genotype-phenotype correlations in RHOBTB2-associated neurodevelopmental disorders
Franziska Langhammer, Reza Maroofian, Rueda Badar, et al.
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of 3
Search research articles
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Showing results (21-30 of 23) with videos related to
Sort By:
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You have reached the last page of results.
This site can display upto 23 results.
American Journal of Medical Genetics. Part A
|
December 23, 2011
Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay
Eric A Muller, Swaroop Aradhya, Joan F Atkin, et al.
American Journal of Human Genetics
|
July 22, 2020
De Novo Variants in the ATPase Module of MORC2 Cause a Neurodevelopmental Disorder with Growth Retardation and Variable Craniofacial Dysmorphism
Maria J Guillen Sacoto, Iva A Tchasovnikarova, Erin Torti, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 11, 2023
Genotype-phenotype correlations in RHOBTB2-associated neurodevelopmental disorders
Franziska Langhammer, Reza Maroofian, Rueda Badar, et al.
Page
of 3