Connection

CHRISTOPHER GROCHOWSKI to Congenital Abnormalities

This is a "connection" page, showing publications CHRISTOPHER GROCHOWSKI has written about Congenital Abnormalities.
  1. De Novo Complex Genomic Rearrangement Spanning 2q31.1 in a Proband With Congenital Malformations: Genotype-Phenotype Correlation and Development of a CGR Detection Pipeline. Am J Med Genet A. 2026 Aug; 200(8):1832-1841.
    View in: PubMed
    Score: 0.181
  2. Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-K?ster-Hauser syndrome. HGG Adv. 2023 07 13; 4(3):100188.
    View in: PubMed
    Score: 0.037
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.