Search

Search Constraints

You searched for: Author/Creator Basinger, Alice

Search Results

1. Cover Image, Volume 176A, Number 4, April 2018. Issue 4 (25th March 2018)

2. Natural history and genotype‐phenotype correlations in 72 individuals with SATB2‐associated syndrome. Issue 4 (13th February 2018)

3. Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy. (5th October 2017)

4. FBXO28 causes developmental and epileptic encephalopathy with profound intellectual disability. (6th December 2020)