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Whole exome sequencing and array-based molecular karyotyping as aids to prenatal diagnosis in fetuses with suspected Simpson-Golabi-Behmel syndrome.
Prenat Diagn. 2016 Oct;36(10):961-965. doi: 10.1002/pd.4920. Epub 2016 Sep 27.
Prenat Diagn. 2016.
PMID: 27589329
Array-CGH and quantitative PCR genetic analysis in a case with bilateral hypoplasia of pulmonary arteries and lungs and simultaneous unilateral renal agenesis.
Hussein K, Steinemann D, Scholz H, Menkhaus R, Feist H, Kreipe H.
Hussein K, et al. Among authors: menkhaus r.
Int J Clin Exp Pathol. 2010 Aug 18;3(7):723-9.
Int J Clin Exp Pathol. 2010.
PMID: 20830244
Free PMC article.
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