Works matching Ellis-van Creveld syndrome
Results: 202
Ellis-van Creveld syndrome: systemic and oral findings.
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- 2012
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- Publication type:
- Case Study
Growth charts for children with Ellis-van Creveld syndrome.
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- 2011
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- Publication type:
- journal article
Cardiac diagnoses, procedures, and healthcare utilisation in inpatients with Ellis-van Creveld syndrome.
- Published in:
- 2015
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- Publication type:
- journal article
Exotropia in a case of Ellis Van Creveld syndrome: A rare case report.
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- 2022
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- journal article
Ellis-Van Creveld syndrome in siblings: A rare case report.
- Published in:
- 2016
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- Publication type:
- Case Study
Ellis-van Creveld syndrome associated with chronic intestinal pseudo-obstruction.
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- Pediatrics International, 2016, v. 58, n. 1, p. 64, doi. 10.1111/ped.12846
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- Article
Ellis-van Creveld Syndrome: A Case Report of Two Brothers.
- Published in:
- 2016
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- Publication type:
- Case Study
Ellis--van Creveld syndrome with facial dysmorphic features in an Egyptian child.
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- Egyptian Journal of Medical Human Genetics, 2010, v. 11, n. 2, p. 181, doi. 10.1016/j.ejmhg.2010.05.001
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- Article
Liver transplantation in Ellis–van Creveld syndrome: A case report.
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- Pediatric Transplantation, 2002, v. 6, n. 3, p. 255, doi. 10.1034/j.1399-3046.2002.01085.x
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- Article
Ellis-van Creveld syndrome with facial hemiatrophy.
- Published in:
- 2010
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- Publication type:
- Case Study
Ellis-van Creveld syndrome: A rare clinical entity.
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- Journal of Oral & Maxillofacial Pathology (0973029X), 2013, v. 17, n. 1, p. 132, doi. 10.4103/0973-029X.110716
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- Article
Clinical manifestations of Ellis-van Creveld syndrome.
- Published in:
- 2009
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- Publication type:
- Case Study
Ellis-van Creveld syndrome: A case report.
- Published in:
- 2008
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- Publication type:
- Case Study
Novel mutations in EVC cause aberrant splicing in Ellis-van Creveld syndrome.
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- Molecular Genetics & Genomics, 2016, v. 291, n. 2, p. 863, doi. 10.1007/s00438-015-1151-2
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- Publication type:
- Article
Increased first-trimester fetal nuchal translucency thickness in association with chondroectodermal dysplasia (Ellis-Van Creveld syndrome).
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- Ultrasound in Obstetrics & Gynecology, 2005, v. 25, n. 4, p. 412, doi. 10.1002/uog.1849
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- Publication type:
- Article
First trimester prenatal diagnosis of chondroectodermal dysplasia (Ellis–van Creveld syndrome) with ultrasound.
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- Ultrasound in Obstetrics & Gynecology, 2001, v. 17, n. 1, p. 86, doi. 10.1046/j.1469-0705.2001.00255.x
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- Publication type:
- Article
Ellis–van Creveld Syndrome in Grey Alpine Cattle.
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- Veterinary Pathology, 2015, v. 52, n. 5, p. 957, doi. 10.1177/0300985815588610
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- Publication type:
- Article
Biallelic mutations in DYNC2LI1 are a rare cause of Ellis‐van Creveld syndrome.
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- Clinical Genetics, 2018, v. 93, n. 3, p. 632, doi. 10.1111/cge.13128
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- Article
Ellis-van Creveld syndrome with unusual oral and dental findings: A rare clinical entity.
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- Dental Research Journal, 2016, v. 13, n. 2, p. 193, doi. 10.4103/1735-3327.178213
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- Article
Report of Ellis–Van Creveld Syndrome: A Chondroectodermal Dysplasia.
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- Journal of Advances in Medical & Biomedical Research, 2023, v. 31, n. 145, p. 207, doi. 10.30699/jambs.31.145.207
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- Article
Severe Hydrocephalus in an Infant with Ellis–van Creveld Syndrome: A Rare Entity.
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- Journal of Pediatric Neurosciences, 2023, v. 18, n. 3, p. 340, doi. 10.4103/jpn.JPN_79_22
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- Article
Ellis-van Creveld Syndrome and Congenital Heart Defects: Presentation of an Additional 32 Cases.
- Published in:
- 2011
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- Publication type:
- Report
Ellis-van creveld syndrome accompanied by cleft glans penis-epispadias: a case report.
- Published in:
- 2016
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- Publication type:
- Case Study
Ellis-Van Creveld Syndrome with Syndrome X - A Rare Association from the Indian Subcontinent.
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- Journal of Pediatric Endocrinology & Metabolism, 2010, v. 23, n. 1/2, p. 189, doi. 10.1515/JPEM.2010.23.1-2.189
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- Publication type:
- Article
Oral abnormalities in the Ellis-van Creveld syndrome.
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- Indian Journal of Dental Research, 2010, v. 21, n. 1, p. 143, doi. 10.4103/0970-9290.62791
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- Article
Oral manifestations in Ellis-van Creveld syndrome: a case report.
- Published in:
- 2018
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- Publication type:
- Case Study
Patient Report Atypical crossed polydactyly in two siblings with Ellis-van Creveld Syndrome and mild clinical manifestations in close relatives.
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- Pediatrics International, 2004, v. 46, n. 2, p. 184, doi. 10.1046/j.1442-200x.2004.01871.x
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- Article
Oral Manifestations in Ellis-van Creveld Syndrome: Report of Five Cases.
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- Pediatric Dentistry, 2004, v. 26, n. 3, p. 277
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- Article
Ellis Van Creveld syndrome.
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- Journal of the Indian Society of Pedodontics & Preventive Dentistry, 2007, p. S5, doi. 10.4103/0970-4388.34737
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- Article
Ellis-Van Creveld syndrome: dental management considerations and description of a new oral finding.
- Published in:
- 2015
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- Publication type:
- journal article
Oral manifestations of Ellis-van Creveld syndrome.
- Published in:
- Contemporary Clinical Dentistry, 2012, v. 3, n. Supp 1, p. S55, doi. 10.4103/0976-237X.95106
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- Article
Ellis-van Creveld Syndrome Associated with Complete Situs Inversus.
- Published in:
- Clinical Pediatrics, 1969, v. 8, n. 6, p. 366, doi. 10.1177/000992286900800613
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- Article
Ellis-van Creveld Syndrome.
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- Clinical Pediatrics, 1966, v. 5, n. 7, p. 431, doi. 10.1177/000992286600500711
- Publication type:
- Article
Ellis-van Creveld syndrome: its history.
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- Pediatric Radiology, 2013, v. 43, n. 8, p. 1030, doi. 10.1007/s00247-013-2709-y
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- Article
Contemporary management of congenital malformations of the heart in infants with Ellis – van Creveld syndrome: a report of nine cases.
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- Cardiology in the Young, 2011, v. 21, n. 2, p. 145, doi. 10.1017/S1047951110001587
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- Article
Adult Survival in Ellis-van Creveld Syndrome with Common Atrium -- A Rare Case Report.
- Published in:
- 2017
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- Publication type:
- Case Study
Ellis van Creveld syndrome with unusual association of essential infantile esotropia.
- Published in:
- 2010
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- Publication type:
- Case Study
Chondroectodermal dysplasia (Ellis-van Creveld syndrome): a case report.
- Published in:
- 2010
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- Publication type:
- Case Study
Ellis-van Creveld Syndrome: A Rare Clinical Report of Oral Rehabilitation by Interdisciplinary Approach.
- Published in:
- Case Reports in Dentistry, 2018, p. 1, doi. 10.1155/2018/8631602
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- Publication type:
- Article
Ellis-van Creveld syndrome and profound deafness resulted by sequence variants in the EVC/EVC2 and TMC1 genes.
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- Journal of Genetics, 2017, v. 96, n. 6, p. 1005, doi. 10.1007/s12041-017-0868-6
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- Article
Oral and dental anomalies in Ellis van Creveld syndrome (chondroectodermal dysplasia): report of a case.
- Published in:
- International Journal of Paediatric Dentistry, 1998, v. 8, n. 2, p. 153, doi. 10.1046/j.1365-263X.1998.00069.x
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- Article
Ellis-van Creveld Syndrome: Mutations Uncovered in Lebanese Families.
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- Case Reports in Genetics, 2015, v. 2015, p. 1, doi. 10.1155/2015/528481
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- Publication type:
- Article
Ellis-Van Creveld syndrome.
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- Orphanet Journal of Rare Diseases, 2007, v. 2, p. 27, doi. 10.1186/1750-1172-2-27
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- Article
Ellis-van Creveld Syndrome and Dyserythropoiesis.
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- Archives of Pathology & Laboratory Medicine, 2005, v. 129, n. 5, p. 680, doi. 10.5858/2005-129-0680-ecsad
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- Publication type:
- Article
THE ELLIS VAN CREVELD SYNDROME.
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- Long-Term Care Nursing / Pielegniarstwo w Opiece Dlugoterminowej, 2023, v. 8, n. 3, p. 3, doi. 10.19251/pwod/2023.3(1)
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- Article
Ellis-van Creveld syndrome.
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- Anaesthesiologie & Intensivmedizin, 2022, v. 63, p. S30, doi. 10.19224/ai2022.S030
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- Publication type:
- Article
Anaesthesia recommendations for Ellis-van Creveld syndrome.
- Published in:
- Anaesthesiologie & Intensivmedizin, 2022, v. 63, n. 2, p. S30, doi. 10.19224/ai2022.S030
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- Publication type:
- Article
Chondroectodermal Dysplasia (Ellis-van Creveld Syndrome).
- Published in:
- Clinical Pediatrics, 1967, v. 6, n. 1, p. 51, doi. 10.1177/000992286700600115
- By:
- Publication type:
- Article
Congenital Heart Disease in an Adult with the Ellis--van Creveld Syndrome.
- Published in:
- Annals of Internal Medicine, 1962, v. 57, n. 5, p. 829, doi. 10.7326/0003-4819-57-5-829
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- Publication type:
- Article
Sequencing EVC and EVC2 identifies mutations in two-thirds of Ellis–van Creveld syndrome patients.
- Published in:
- Human Genetics, 2006, v. 120, n. 5, p. 663, doi. 10.1007/s00439-006-0237-7
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- Publication type:
- Article