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multiple congenital anomalies
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Gastroschisis and associated defects: an international study
2007 |
Third Faculty of Medicine
publication
PAICS deficiency, a new defect of de novo purine synthesis resulting in multiple congenital anomalies and fatal outcome
2019 |
First Faculty of Medicine
publication
Deletions of 9q21.3 Including NTRK2 Are Associated With Severe Phenotype
2015 |
Second Faculty of Medicine
publication
Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome
2014 |
Second Faculty of Medicine
publication
De novo SMARCA2 variants clustered outside the helicase domain cause a new recognizable syndrome with intellectual disability and blepharophimosis distinct from Nicolaides-Baraitser syndrome
2020 |
Second Faculty of Medicine
publication
Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations
2008 |
Second Faculty of Medicine