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Acrocephalosyndactylia
Pfeiffer Syndrome Type II Discovered Perinatally
Improving Diagnosis and Treatment of Craniofacial Malformations Utilizing Animal Models
Date Due Date Due Date Due
(12) United States Patent (10) Patent No.: US 8,853,266 B2 Dalton Et Al
Lessons Learned
Chiari I Malformation in Patients with Pfeiffer Syndrome
26 April 2010 TE Prepublication Page 1 Nomina Generalia General Terms
Rare Case Report of Ambiguous Genitalia with Apert Syndrome
The Role of Genetic Mutations in Genes FGFR1 & FGFR2 in Pfeiffer
The Role of Genetic Factors in the Human Face, Jaws and Teeth: a Review
Chid Neurolog7 Naheee.Indd
' the Patient, a 53-Year-Old Female, Was Born with a Left Unilateral
Orphanet Journal of Rare Diseases Biomed Central
Apert Syndrome: a Case Report
1987 Meeting of the Craniofacial Society Of
ABSTRACTS BARNETT R, SHUSTERMAN S. Fetal Alcohol
Pfeiffer Syndrome: Clinical and Genetic Findings in Five Brazilian Families
Patient Present Sever Sign Segment Upper Develop Differ Studi Syndrom
Top View
A Case of Pfeiffer Syndrome
Mesh Terms for 2002
' Reprints: Peggy Mccardle, Ph.D. Exceptional Family Member Program Department of Pediatrics Walter Reed Army Medical Center Washington, D.C
Apert Syndrome: a Case Report Apert Syndrome: a Case Report
Bilaga 3 Sökdokumentation Till Tandvårdsstöd F - Systematiska Översikter
Identification of Human Genes and Its Genomics Functions Via Mirnas of C
OBSERVATIONS and COMMENTARY the State of What
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General and Oral Aspects in Apert Syndrome: Report of a Case
Long-Term Results in Syndromic Craniosynostosis
General and Oral Aspects in Apert Syndrome: Report of a Case
Genetics of Craniosynostosis: Review of the Literature
Supplemental Material Placed on This Supplemental Material Which Has Been Supplied by the Author(S) BMJ Support Palliat Care