9 results on '"De Mas, Philippe"'
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2. Genotype-Phenotype Correlations in Charcot-Marie-Tooth Disease Type 2 Caused by Mitofusin 2 Mutations
3. Double deletion of a chromosome 21 inserted in a chromosome 22 in an azoospermic patient
4. Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
5. Subtelomeric 6p deletion: Clinical, FISH, and array CGH characterization of two cases
6. Cytogenetic Investigations of Infertile Men With Low Sperm Counts: A 25‐Year Experience
7. Increased aneuploidy in spermatozoa from testicular tumour patients after chemotherapy with cisplatin, etoposide and bleomycin.
8. Subtelomeric 6p deletion: Clinical, FISH, and array CGH characterization of two cases
9. Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
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