Connection

IGNATIA VAN DEN VEYVER to Genetic Variation

This is a "connection" page, showing publications IGNATIA VAN DEN VEYVER has written about Genetic Variation.
Connection Strength

0.167
  1. Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders. Cold Spring Harb Perspect Med. 2015 Aug 07; 5(10).
    View in: PubMed
    Score: 0.071
  2. Genome-wide array-based copy number profiling in human placentas from unexplained stillbirths. Prenat Diagn. 2011 Oct; 31(10):932-44.
    View in: PubMed
    Score: 0.053
  3. Loss of holocytochrome c-type synthetase causes the male lethality of X-linked dominant microphthalmia with linear skin defects (MLS) syndrome. Hum Mol Genet. 2002 Dec 01; 11(25):3237-48.
    View in: PubMed
    Score: 0.029
  4. PORCN mutations and variants identified in patients with focal dermal hypoplasia through diagnostic gene sequencing. Genet Test Mol Biomarkers. 2010 Oct; 14(5):709-13.
    View in: PubMed
    Score: 0.013
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.