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Prenatal diagnosis of MPPH syndrome.
De Keersmaecker B, Van Esch H, Van Schoubroeck D, Claus F, Moerman P, De Catte L. De Keersmaecker B, et al. Among authors: moerman p. Prenat Diagn. 2013 Mar;33(3):292-5. doi: 10.1002/pd.4039. Epub 2013 Jan 24. Prenat Diagn. 2013. PMID: 23348821
Chromosome 22q11 deletion presenting as the Potter sequence.
Devriendt K, Moerman P, Van Schoubroeck D, Vandenberghe K, Fryns JP. Devriendt K, et al. Among authors: moerman p. J Med Genet. 1997 May;34(5):423-5. doi: 10.1136/jmg.34.5.423. J Med Genet. 1997. PMID: 9152843 Free PMC article.
Semilobar holoprosencephaly in a 46,XY female fetus.
Witters I, Moerman P, Muenke M, Van Assche FA, Devriendt K, Legius E, Van Schoubroeck D, Fryns JP. Witters I, et al. Among authors: moerman p. Prenat Diagn. 2001 Oct;21(10):839-41. doi: 10.1002/pd.151. Prenat Diagn. 2001. PMID: 11746125
349 results