MG-200 The clinical utility of targeted next generation sequencing in prenatal congenital heart disease
MG-200 The clinical utility of targeted next generation sequencing in prenatal congenital heart disease Did Not Attend
MG-200 The clinical utility of targeted next generation sequencing in prenatal congenital heart disease Poor
MG-200 The clinical utility of targeted next generation sequencing in prenatal congenital heart disease Fair
MG-200 The clinical utility of targeted next generation sequencing in prenatal congenital heart disease Good
MG-200 The clinical utility of targeted next generation sequencing in prenatal congenital heart disease Very Good
MG-200 The clinical utility of targeted next generation sequencing in prenatal congenital heart disease Excellent
MG-201 7p22.3p22.2 microdeletion is associated with variable developmental delay and characteristic facial features
MG-201 7p22.3p22.2 microdeletion is associated with variable developmental delay and characteristic facial features Did Not Attend
MG-201 7p22.3p22.2 microdeletion is associated with variable developmental delay and characteristic facial features Poor
MG-201 7p22.3p22.2 microdeletion is associated with variable developmental delay and characteristic facial features Fair
MG-201 7p22.3p22.2 microdeletion is associated with variable developmental delay and characteristic facial features Good
MG-201 7p22.3p22.2 microdeletion is associated with variable developmental delay and characteristic facial features Very Good
MG-201 7p22.3p22.2 microdeletion is associated with variable developmental delay and characteristic facial features Excellent
MG-202 A new case of 5q31 microdeletion syndrome and putative causative genes
MG-202 A new case of 5q31 microdeletion syndrome and putative causative genes Did Not Attend
MG-202 A new case of 5q31 microdeletion syndrome and putative causative genes Poor
MG-202 A new case of 5q31 microdeletion syndrome and putative causative genes Fair
MG-202 A new case of 5q31 microdeletion syndrome and putative causative genes Good
MG-202 A new case of 5q31 microdeletion syndrome and putative causative genes Very Good
MG-202 A new case of 5q31 microdeletion syndrome and putative causative genes Excellent
MG-203 ALG9-CDG: New Clinical Case and Review of the Literature
MG-203 ALG9-CDG: New Clinical Case and Review of the Literature Did Not Attend
MG-203 ALG9-CDG: New Clinical Case and Review of the Literature Poor
MG-203 ALG9-CDG: New Clinical Case and Review of the Literature Fair
MG-203 ALG9-CDG: New Clinical Case and Review of the Literature Good
MG-203 ALG9-CDG: New Clinical Case and Review of the Literature Very Good
MG-203 ALG9-CDG: New Clinical Case and Review of the Literature Excellent
MG-204 A rare four break balanced reciprocal insertional chromosomal translocation – a case report
MG-204 A rare four break balanced reciprocal insertional chromosomal translocation – a case report Did Not Attend
MG-204 A rare four break balanced reciprocal insertional chromosomal translocation – a case report Poor
MG-204 A rare four break balanced reciprocal insertional chromosomal translocation – a case report Fair
MG-204 A rare four break balanced reciprocal insertional chromosomal translocation – a case report Good
MG-204 A rare four break balanced reciprocal insertional chromosomal translocation – a case report Very Good
MG-204 A rare four break balanced reciprocal insertional chromosomal translocation – a case report Excellent
MG-205 Novel WDR45 mutation identified in patient diagnosed with Beta-propeller protein associated neurodegeneration
MG-205 Novel WDR45 mutation identified in patient diagnosed with Beta-propeller protein associated neurodegeneration Did Not Attend
MG-205 Novel WDR45 mutation identified in patient diagnosed with Beta-propeller protein associated neurodegeneration Poor
MG-205 Novel WDR45 mutation identified in patient diagnosed with Beta-propeller protein associated neurodegeneration Fair
MG-205 Novel WDR45 mutation identified in patient diagnosed with Beta-propeller protein associated neurodegeneration Good
MG-205 Novel WDR45 mutation identified in patient diagnosed with Beta-propeller protein associated neurodegeneration Very Good
MG-205 Novel WDR45 mutation identified in patient diagnosed with Beta-propeller protein associated neurodegeneration Excellent
MG-206 Novel HPD mutations identified in First Nations Canadian siblings diagnosed with Tyrosinemia Type III
MG-206 Novel HPD mutations identified in First Nations Canadian siblings diagnosed with Tyrosinemia Type III Did Not Attend
MG-206 Novel HPD mutations identified in First Nations Canadian siblings diagnosed with Tyrosinemia Type III Poor
MG-206 Novel HPD mutations identified in First Nations Canadian siblings diagnosed with Tyrosinemia Type III Fair
MG-206 Novel HPD mutations identified in First Nations Canadian siblings diagnosed with Tyrosinemia Type III Good
MG-206 Novel HPD mutations identified in First Nations Canadian siblings diagnosed with Tyrosinemia Type III Very Good
MG-206 Novel HPD mutations identified in First Nations Canadian siblings diagnosed with Tyrosinemia Type III Excellent