Human Genome Epidemiology Literature Finder
Rare Diseases
|
Records 1 - 1 (of 1 Records) |
| Query Trace: Frontometaphyseal Dysplasia[original query] |
|---|
| The MAP3K7 gene: Further delineation of clinical characteristics and genotype/phenotype correlations. Human mutation 2022 6 43 (10): 1377-1395. van Woerden Geeske M, Senden Richelle, de Konink Charlotte, Trezza Rossella A, Baban Anwar, Bassetti Jennifer A, van Bever Yolande, Bird Lynne M, van Bon Bregje W, Brooks Alice S, Guan Qiaoning, Klee Eric W, Marcelis Carlo, Rosado Joel M, Schimmenti Lisa A, Shikany Amy R, Terhal Paulien A, Nicole Weaver Kathryn, Wessels Marja W, van Wieringen Hester, Hurst Anna C, Gooch Catherine F, Steindl Katharina, Joset Pascal, Rauch Anita, Tartaglia Marco, Niceta Marcello, Elgersma Ype, Demirdas Serw |
- Page last reviewed:Feb 1, 2024
- Content source:

