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Your search keyword '"Brechard, Marie"' showing total 9 results

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9 results on '"Brechard, Marie"'

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1. Evidence for high breakpoint variability in 46, XX, SRY‐positive testicular disorder and frequent ARSE deletion that may be associated with short stature

2. Next‐generation sequencing in a series of 80 fetuses with complex cardiac malformations and/or heterotaxy

3. Strategy for Use of Genome-Wide Non-Invasive Prenatal Testing for Rare Autosomal Aneuploidies and Unbalanced Structural Chromosomal Anomalies

4. Novel CCM2 missense variants abrogating the CCM1–CCM2 interaction cause cerebral cavernous malformations

7. A Broad Test Based on Fluorescent-Multiplex PCR for Noninvasive Prenatal Diagnosis of Cystic Fibrosis

8. The expanding spectrum of COL2A1 gene variants IN 136 patients with a skeletal dysplasia phenotype

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