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Hypomorphic CEP290/NPHP6 mutations result in anosmia caused by the selective loss of G proteins in cilia of olfactory sensory neurons | PNAS
Hypomorphic CEP290/NPHP6 mutations result in anosmia caused by the selective loss of G proteins in cilia of olfactory sensory neurons | PNAS
Nima Rezaei Asghar Aghamohammadi Luigi D. Notarangelo Editors Definition, Diagnosis, and Management Second Edition
Hypomorphic CEP290/NPHP6 mutations result in anosmia caused by the selective loss of G proteins in cilia of olfactory sensory neurons | PNAS
pointe pescade,cours élémentaire 1ère année,ce1, 1947-1948, photos de classes, ozilou;http://alger-roi.fr;venis
Postnatal age-differential ASD-like transcriptomic, synaptic, and behavioral deficits in Myt1l-mutant mice - ScienceDirect
Prenatal Diagnosis of Bardet-Biedl Syndrome: A Case Study and Review of Literature | SpringerLink
Hypomorphic CEP290/NPHP6 mutations result in anosmia caused by the selective loss of G proteins in cilia of olfactory sensory neurons | PNAS
RFX7 is required for the formation of cilia in the neural tube - ScienceDirect
Prenatal diagnosis of Bardet Biedl Syndrome: A case report - ScienceDirect
Large-Scale Deletions and SMADIP1 Truncating Mutations in Syndromic Hirschsprung Disease with Involvement of Midline Structures - ScienceDirect
Postnatal age-differential ASD-like transcriptomic, synaptic, and behavioral deficits in Myt1l-mutant mice - ScienceDirect
Jazz-Rhone-Alpes.com n° 554 du lundi 22 juin 2015
Combined T- and B-Cell Immunodeficiencies | SpringerLink
Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-
Frontiers | Meckel–Gruber Syndrome: An Update on Diagnosis, Clinical Management, and Research Advances
Hypomorphic CEP290/NPHP6 mutations result in anosmia caused by the selective loss of G proteins in cilia of olfactory sensory neurons | PNAS
Prenatal Diagnosis of Bardet-Biedl Syndrome: A Case Study and Review of Literature | SpringerLink
REPORT Identification of CC2D2A as a Meckel Syndrome Gene Adds an Important Piece to the Ciliopathy Puzzle
Large-Scale Deletions and SMADIP1 Truncating Mutations in Syndromic Hirschsprung Disease with Involvement of Midline Structures - ScienceDirect
RFX7 is required for the formation of cilia in the neural tube - ScienceDirect
Liste des candidats dans les communes de plus de 1 000 habitants
Prenatal diagnosis of Bardet Biedl Syndrome: A case report - ScienceDirect
