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31. Understanding the new BRD4‐related syndrome: Clinical and genomic delineation with an international cohort study. Issue 2 (25th April 2022)

32. Whole exome sequencing of men with multiple morphological abnormalities of the sperm flagella reveals novel homozygous QRICH2 mutations. Issue 5 (17th July 2019)

33. Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella. Issue 10 (13th August 2018)

34. Xq22.3q23 microdeletion harboring TMEM164 and AMMECR1 genes: Two case reports confirming a recognizable phenotype with short stature, midface hypoplasia, intellectual delay, and elliptocytosis. Issue 4 (8th February 2019)