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16451. Deleterious effects of gestational diabetes mellitus on the characteristics of the rectus abdominis muscle associated with pregnancy-specific urinary incontinence. (August 2020)

16452. Deleterious variants in CRLS1 lead to cardiolipin deficiency and cause an autosomal recessive multi-system mitochondrial disease. Issue 21 (11th February 2022)

16453. Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2. (18th January 2018)

16454. Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome. Issue 3 (5th November 2015)

16455. Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data. Issue 6 (May 2016)

16459. Delineating the expanding phenotype associated with SCAPER gene mutation. Issue 8 (13th June 2019)

16460. Delineation of dominant and recessive forms of LZTR1‐associated Noonan syndrome. Issue 6 (3rd April 2019)