Craniosynostosis genetics: The mystery unfolds. - Test2 - elhamkhani - TriplyDB

Craniosynostosis genetics: The mystery unfolds.

Craniosynostosis genetics: The mystery unfolds.

http://www.wikidata.org/entity/Q37957083

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Update of Diagnostic Evaluation of Craniosynostosis with a Focus on Pediatric Systematic Evaluation and Genetic Studies Pityriasis rosea in pregnancy: report of a spousal occurrence and craniosynostosis in the healthy newborn Role of 99mTc-ECD SPECT in the management of children with craniosynostosis.Bilateral squamosal suture synostosis: A rare form of isolated craniosynostosis in Crouzon syndrome.Familial incidence and associated symptoms in a population of individuals with nonsyndromic craniosynostosis Characterization of distinct classes of differential gene expression in osteoblast cultures from non-syndromic craniosynostosis bone Apert syndrome with S252W FGFR2 mutation and characterization using Phenomizer: An Indian case report.A novel ciliopathic skull defect arising from excess neural crest Crouzon syndrome - A rare case report.Syndromic craniosynostosis: neuropsycholinguistic abilities and imaging analysis of the central nervous system.Sudden death associated with syndromic craniosynostosis.Craniosynostosis, psychomotor retardation, and facial dysmorphic features in a Spanish patient with a 4q27q28.3 deletion

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P2860

Craniosynostosis genetics: The mystery unfolds.

http://www.wikidata.org/entity/Q37957083

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Craniosynostosis genetics: The mystery unfolds.

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Craniosynostosis genetics: The mystery unfolds.

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Craniosynostosis genetics: The mystery unfolds.

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Craniosynostosis genetics: The mystery unfolds.

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Craniosynostosis genetics: The mystery unfolds.

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Craniosynostosis genetics: The mystery unfolds.

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0971-6866.86171

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Indian Journal of Human Genetics

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Craniosynostosis genetics: The mystery unfolds.

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Pfeiffer syndrome

Ocular phenotype correlations in patients with TWIST versus FGFR3 genetic mutations

The molecular basis of Boston-type craniosynostosis: the Pro148-->His mutation in the N-terminal arm of the MSX2 homeodomain stabilizes DNA binding without altering nucleotide sequence preferences

The origin of EFNB1 mutations in craniofrontonasal syndrome: frequent somatic mosaicism and explanation of the paucity of carrier males

Craniofacial dysmorphology of Carpenter syndrome: lessons from three affected siblings

A recurrent mutation, ala391glu, in the transmembrane region of FGFR3 causes Crouzon syndrome and acanthosis nigricans.

Neurodevelopmental and behavioral abnormalities associated with deletion of chromosome 9p.

Neurodevelopment of children with single suture craniosynostosis: a review.

Molecular and cellular bases of syndromic craniosynostoses.

P450 oxidoreductase deficiency: a new disorder of steroidogenesis with multiple clinical manifestations.

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