Connection

IGNATIA VAN DEN VEYVER to Adolescent

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

0.153
  1. Missed opportunities: unidentified genetic risk factors in prenatal care. Prenat Diagn. 2018 01; 38(1):75-79.
    View in: PubMed
    Score: 0.035
  2. Management of ornithine transcarbamylase deficiency in pregnancy. Am J Perinatol. 2010 Nov; 27(10):775-84.
    View in: PubMed
    Score: 0.021
  3. Non-random X chromosome inactivation in Aicardi syndrome. Hum Genet. 2009 Mar; 125(2):211-6.
    View in: PubMed
    Score: 0.020
  4. Phenotype and management of Aicardi syndrome: new findings from a survey of 69 children. J Child Neurol. 2007 Feb; 22(2):176-84.
    View in: PubMed
    Score: 0.017
  5. Facial and physical features of Aicardi syndrome: infants to teenagers. Am J Med Genet A. 2005 Oct 15; 138A(3):254-8.
    View in: PubMed
    Score: 0.016
  6. Presence of filamin in the astrocytic inclusions of Aicardi syndrome. Pediatr Neurol. 2004 Jan; 30(1):7-15.
    View in: PubMed
    Score: 0.014
  7. Microphthalmia with linear skin defects (MLS), Aicardi, and Goltz syndromes: are they related X-linked dominant male-lethal disorders? Cytogenet Genome Res. 2002; 99(1-4):289-96.
    View in: PubMed
    Score: 0.012
  8. Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome. Brain Dev. 2001 Dec; 23 Suppl 1:S147-51.
    View in: PubMed
    Score: 0.012
  9. A genome-wide screen for copy number alterations in an adolescent pilot cohort with m?llerian anomalies. Fertil Steril. 2015 Feb; 103(2):487-93.
    View in: PubMed
    Score: 0.007
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.