Showing results 1 to 7 of 7
Title | Author(s) | Issue Date | |
---|---|---|---|
2009 | |||
Developmental perspectives on copy number abnormalities of the 22q11.2 region Journal:Clinical Genetics | 2010 | ||
Mosaic Activating Mutations in FGFR1 Cause Encephalocraniocutaneous Lipomatosis Journal:American Journal of Human Genetics | 2016 | ||
Obesity, hypothyroidism, craniosynostosis, cardiac hypertrophy, colitis, and developmental delay: A novel syndrome Journal:American Journal of Medical Genetics, Part A | 2007 | ||
Phenotypic variability of distal 22q11.2 copy number abnormalities Journal:American Journal of Medical Genetics, Part A | 2011 | ||
Registry- and clinic-based analyses of birth defects and syndromes associated with cleft lip/palate in Victoria, Australia Journal:Cleft Palate-Craniofacial Journal | 2009 | ||
Tumour surveillance in Beckwith-Wiedemann syndrome and hemihyperplasia: A critical review of the evidence and suggested guidelines for local practice Journal:Journal of Paediatrics and Child Health | 2006 |