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Your search keyword '"Gérard-Blanluet, Marion"' showing total 19 results

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19 results on '"Gérard-Blanluet, Marion"'

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1. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

2. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

3. Hypophosphatasia: molecular testing of 19 prenatal cases and discussion about genetic counseling†

8. High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters

10. Genomic imbalances detected by array-CGH in patients with syndromal ocular developmental anomalies

11. Aphallia, Lung Agenesis and Multiple Defects of Blastogenesis

13. Classical West “syndrome” phenotype with a subtelomeric 4p trisomy

15. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

16. Mosaic trisomy 9 and lobar holoprosencephaly

17. CEMARA an information system for rare diseases.

18. CEMARA an information system for rare diseases.

19. [X fragile syndrome; how to make a precocious diagnostic].

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