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- A Survey of Phenotypic Features in Juvenile Polyposis J Med Genet: First Published As 10.1136/Jmg.35.6.476 on 1 June 1998
- The Causes of Congenital Club Foot
- Minor Anomalies
- Oral-Facial-Digital Syndromes by Joseph R Siebert Phd (Dr
- Treacher Collins Syndrome: a Brief Review on Diagnostic Aids and Review of Literature with a Case Description
- Heart Defects, Laryngeal Anomahes, Preaxial Polydactyly, and Colonic Agangbonosis M Sibs
- Syndromic and Nonsyndromic Systemic Associations of Congenital Lacrimal Drainage Anomalies: a Major Review
- Genetic Disorders Associated with Macrocephaly
- GLI3 Gene GLI Family Zinc Finger 3
- Boards' Fodder
- Coexisting Edward Syndrome and Klinefelter Syndrome
- Are Patients with Loeys-Dietz Syndrome Misdiagnosed with Beals Syndrome? Rebecca Woolnough, Andrew Dhawan, Kimberly Dow and Jagdeep S
- SAS Journal of Surgery Incomplete Ectrodactyly
- Analyzing the Physical, Educational, Social and Visual Needs of a Patient with Crouzon Syndrome: a Case Study
- Craniosynostosis HAIDAR KABBANI, M.D., and TALKAD S
- Syndromes Associated with Congenital Cardiac Defects Scope (Staff): Nursing and Medical Staff Scope (Area): NICU KEMH, NICU PCH, NETS WA
- Crouzon Syndrome with Ocular Abnormalities: a Case Report
- FGFR1 Mutations Cause Hartsfield Syndrome, the Unique Association
- The First Arch Syndrome
- A Variant of Freeman-Sheldon Syndrome
- Craniofacial Surgery for Orbital Malformations D Richardson and JK Thiruchelvam 1225
- Title: Oral-Facial-Digital Syndrome Type 1 Genereview – Table 1 Authors
- Craniofacial Syndromes and Malformations Marilyn T
- Crouzon Syndrome
- Syndromic Disorders with Short Stature Zeynep Şıklar, Merih Berberoğlu Ankara University School of Medicine, Department of Pediatric Endocrinology, Ankara, Turkey
- Cenani–Lenz Syndactyly with Facial Dysmorphism, Hypothyroidism, and Renal Hypoplasia: a Case Report Hisham Jarbhoua, Hanan Hamamya, Azmy Al-Hadidyb and Kamel Ajlounia
- Crouzon Syndrome: an Experience of Surgical Intervention at Bangabandhu Sheikh Mujib Medical University, Bangladesh
- CROUZON SYNDROME This Syndrome Was Originally Described in 1912 by a French Neuro- Surgeon
- A Clinical Study of 31 Individuals with Midline Facial Defects with Hypertelorism and a Guideline for Follow-Up
- Syndromes with Cleft Lip and Cleft Palate M. MICHAEL COHEN, JR., D.M.D
- Management of Orbital Hypertelorism
- Acampomelic Campomelic Dysplasia in Genetic Male Without Sex Reversal
- Syndrome Spotter Syndrome Spotter
- Congenital Cataract and Multisystem Disorders
- Orofacial Features of Treacher Collins Syndrome
- Orbital Osteotomy for Hypertelorism
- Syndromes Presenting Adducted Thumb With/ Without Clubfoot and Dundar Syndrome
- Crouzon Syndrome: Report in a Family Dentistry Section
- Craniosynostosis
- Etiologies Related to Deafblindness and Hear Ing Loss This Is a List of Syndromes and Conditions That May Cause a Combined Vision and DEAFBLINDNESS Hearing Loss
- Treacher Collins Syndrome: a Case Report and Review of Literature
- 201603290310030File .Pdf
- Mb on Chromosome 2Q14.1&Am
- Chromosome Abnormalities Reference
- Novel Heterozygous Mutation in the Extracellular Domain of FGFR1 Associated with Hartsfield Syndrome
- OCULO-Orbital Manifestations of Crouzon Syndrome- a Rare Case Report
- Autosomal Trisomy Syndromes: a Detailed Study of 27 Cases of Edwards' Syndrome and 27 Cases of Patau's Syndrome ANGELA I