Works matching DE "SYNDACTYLY"
Results: 200
Fraser Syndrome: Affected Siblings Born to Nonconsanguineous Parents and Diagnosed at Autopsy.
- Published in:
- Pediatric & Developmental Pathology, 2008, v. 11, n. 3, p. 220, doi. 10.2350/07-04-0254.1
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- Publication type:
- Article
Asterixis in the leg induced by anterior cerebral artery infarction.
- Published in:
- 2016
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- Publication type:
- journal article
P03.03: Early diagnosis of Greig cephalopolysyndactyly syndrome.
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- Ultrasound in Obstetrics & Gynecology, 2012, v. 40, p. 179, doi. 10.1002/uog.11789
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- Article
Prenatal Diagnosis of a 2.5 Mb De Novo 17q24.1q24.2 Deletion Encompassing KPNA2 and PSMD12 Genes in a Fetus with Craniofacial Dysmorphism, Equinovarus Feet, and Syndactyly.
- Published in:
- 2017
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- Publication type:
- Case Study
MORPHOLOGICAL STUDY OF FETUS WITH FRASER SYNDROME. A CASE REPORT.
- Published in:
- 2015
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- Publication type:
- Case Study
Unilateral cleft hand' lobster-claw deformity) ;A case report.
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- Journal of Chinese Clinical Medicine, 2009, v. 4, n. 6, p. 329
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- Publication type:
- Article
Crossed polydactyly and Greig cephalopolysyndactyly syndrome.
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- Indian Pediatrics, 2013, v. 50, n. 10, p. 967, doi. 10.1007/s13312-013-0240-8
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- Article
Fraser Syndrome with Partial Anomalous Pulmonary Venous Connection.
- Published in:
- 2008
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- Publication type:
- Case Study
Commentary on Hardwicke et al. Macrodactyly – options and outcomes.
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- Journal of Hand Surgery (17531934), 2013, v. 38, n. 3, p. 304, doi. 10.1177/1753193413476410
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- Article
Commentary on Kim et al. Characteristic radiographic features of the central ray in Apert syndrome.
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- Journal of Hand Surgery (17531934), 2013, v. 38, n. 3, p. 265, doi. 10.1177/1753193412471107
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- Article
Characteristic radiographic features of the central ray in Apert syndrome.
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- Journal of Hand Surgery (17531934), 2013, v. 38, n. 3, p. 257, doi. 10.1177/1753193412462895
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- Publication type:
- Article
Long-term aesthetic outcome of fingertip reconstruction in complete syndactyly release.
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- Journal of Hand Surgery (17531934), 2013, v. 38, n. 3, p. 281, doi. 10.1177/1753193412461583
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- Publication type:
- Article
Keloid formation after syndactyly release in patients with associated macrodactyly: management with methotrexate therapy.
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- Journal of Hand Surgery (17531934), 2011, v. 36, n. 6, p. 490, doi. 10.1177/1753193411402146
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- Publication type:
- Article
Syndactyly Correction: an Aesthetic Reconstruction.
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- Journal of Hand Surgery (17531934), 2010, v. 35, n. 6, p. 446, doi. 10.1177/1753193410362638
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- Publication type:
- Article
A Modification of the Chinese Island Flap Technique for Simple Incomplete Syndactyly Release.
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- Journal of Hand Surgery (17531934), 2009, v. 34, n. 1, p. 99, doi. 10.1177/1753193408094708
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- Publication type:
- Article
Expression of Familial Middle–Ring–Little Finger Syndactyly as Either Simple Syndactyly or Synpolydactyly
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- Journal of Hand Surgery (17531934), 2006, v. 31, n. 1, p. 118, doi. 10.1016/j.jhsb.2005.07.006
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- Publication type:
- Article
Ectodermal dysplasia-cutaneous syndactyly syndrome maps to chromosome 7p21.1-p14.3.
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- Human Genetics, 2009, v. 125, n. 4, p. 421, doi. 10.1007/s00439-009-0640-y
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- Publication type:
- Article
Brown Tumour of Posterior Maxilla Associated with Polydactyly, Syndactyly and Cardiac Anomalies: A Unique Case Report.
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- 2014
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- Publication type:
- Case Study
Non-Syndromic Occurrence of Multiple Dental and Skeletal Anomalies: A Rare Case Report and Brief Literature Review.
- Published in:
- 2014
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- Publication type:
- Case Study
Intrauterine heterotopic Heterotopic reimplantation Reimplantation of an amputated Amputated finger Finger due to the amniotic Amniotic band Band syndrome Syndrome.
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- Research in Medicine: Journal of Research in Medical Sciences, 2020, v. 44, n. 2, p. 391
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- Publication type:
- Article
Surgical treatment outcomes in patients with syndactyly in Imam Khomeini Hospital in Tehran, Iran during 1996-2011: a breif report.
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- Tehran University Medical Journal, 2011, v. 69, n. 8, p. 518
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- Publication type:
- Article
Apert Sendromu: Olgu Sunumu.
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- 2009
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- Publication type:
- Case Study
A Dermatoglyphic Study in Cases of Polydactyly and Syndactyly.
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- Anil Aggrawal's Internet Journal of Forensic Medicine & Toxicology, 2010, v. 11, n. 1, p. 4
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- Publication type:
- Article
Oculodentodigital Dysplasia Presenting as Spastic Ataxic Syndrome in an Indian Patient.
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- Annals of Indian Academy of Neurology, 2025, v. 28, n. 1, p. 112, doi. 10.4103/aian.aian_166_24
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- Publication type:
- Article
A rare association with suffered cardiac arrest, long QT interval, and syndactyly: Timothy syndrome (LQT-8).
- Published in:
- 2015
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- Publication type:
- Case Study
Molecular analysis of exons 8, 9 and 10 of the fibroblast growth factor receptor 2 (FGFR2) gene in two families with index cases of Apert Syndrome.
- Published in:
- 2015
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- Publication type:
- Case Study
Intraoperative tissue expansion as an alternative approach for hand syndactyly management to avoid skin grafts in children.
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- Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2018, v. 75, n. 3, p. 290, doi. 10.2298/VSP160624347K
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- Publication type:
- Article
Can intravenous acetaminophen reduce the needs to more opioids to control pain in intubated patients?
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- Indian Journal of Critical Care Medicine, 2016, v. 20, n. 8, p. 465, doi. 10.4103/0972-5229.188197
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- Publication type:
- Article
The bovine aristaless-like homeobox 4 (ALX4) as a candidate gene for syndactyly.
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- Cytogenetic & Genome Research, 2006, v. 115, n. 2, p. 123, doi. 10.1159/000095231
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- Publication type:
- Article
Síndrome de Apert con agenesia renal, ¿una rara asociación?
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- Revista Mexicana de Pediatria, 2014, v. 81, n. 1, p. 18
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- Publication type:
- Article
Sfrp2 is a transcriptional target of SREBP-1 in mouse chondrogenic cells.
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- Molecular & Cellular Biochemistry, 2015, v. 406, n. 1/2, p. 163, doi. 10.1007/s11010-015-2434-y
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- Publication type:
- Article
Tetra-amelia with lung hypoplasia and facial clefts, Roberts-SC syndrome: report of two cases.
- Published in:
- 2010
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- Publication type:
- journal article
A Review of the Genetics and Pathogenesis of Syndactyly in Humans and Experimental Animals: A 3-Step Pathway of Pathogenesis.
- Published in:
- BioMed Research International, 2019, p. 1, doi. 10.1155/2019/9652649
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- Publication type:
- Article
Diagnosis of Joubert Syndrome 10 in a Fetus with Suspected Dandy-Walker Variant by WES: A Novel Splicing Mutation in OFD1.
- Published in:
- BioMed Research International, 2018, p. 1, doi. 10.1155/2018/4032543
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- Publication type:
- Article
ASK TWICE FOR RAYNAUD'S DISEASE BEFORE HAND SURGERY.
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- Turkish Journal of Plastic Surgery, 2012, v. 20, n. 1, p. 33
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- Publication type:
- Article
A nonsense mutation in the HOXD13 gene underlies synpolydactyly with incomplete penetrance.
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- Journal of Human Genetics, 2011, v. 56, n. 10, p. 701, doi. 10.1038/jhg.2011.84
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- Publication type:
- Article
Mutation in PVRL4 gene encoding nectin-4 underlies ectodermal-dysplasia-syndactyly syndrome (EDSS1).
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- Journal of Human Genetics, 2011, v. 56, n. 5, p. 352, doi. 10.1038/jhg.2011.18
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- Publication type:
- Article
A syndactyly type IV locus maps to 7q36.
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- Journal of Human Genetics, 2007, v. 52, n. 6, p. 561, doi. 10.1007/s10038-007-0150-5
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- Publication type:
- Article
Anaesthesia in Poland syndrome: A case report.
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- Journal of Clinical & Experimental Investigations, 2014, v. 5, n. 4, p. 608, doi. 10.5799/ahinjs.01.2014.04.0468
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- Publication type:
- Article
Oculodentodigital Dysplasia Diagnosed from Severe Hypotrichosis.
- Published in:
- 2019
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- Publication type:
- Case Study
Triploidy and Routine Combined First Trimester Pregnancy Screening.
- Published in:
- Avicenna Journal of Medical Biotechnology, 2019, v. 11, n. 1, p. 124
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- Publication type:
- Article
Genetics Corner: A Consultation for Familial Polysyndactyly.
- Published in:
- Neonatology Today, 2024, v. 19, n. 6, p. 171
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- Publication type:
- Article
Clinical Pearl: Fentanyl Exposure Syndrome.
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- Neonatology Today, 2023, v. 18, n. 12, p. 189
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- Publication type:
- Article
Osteomyelitis Due to Aspergillus flavus in an Immunocompetent Child with Fatco Syndrome: A Case Report and Literature Review.
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- Journal of Pediatric Infection / Çocuk Enfeksiyon Dergisi, 2012, v. 6, n. 4, p. 163, doi. 10.5152/ced.2012.46
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- Publication type:
- Article
Greig Cephalopolysyndactyly Syndrome: A Case Report.
- Published in:
- 2011
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- Publication type:
- Case Study
Ektrodaktili Ektodermal Displazi-Klefting Sendromlu Ailesel Üç Olgu.
- Published in:
- Archives of the Turkish Dermatology & Venerology / Turkderm, 2012, v. 46, n. 1, p. 47, doi. 10.4274/turkderm.65707
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- Publication type:
- Article
Fraser sendromu: Bir vaka takdimi.
- Published in:
- Cocuk Sagligi ve Hastaliklari Dergisi, 2013, v. 56, n. 1, p. 20
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- Publication type:
- Article
Successful, Full-Thickness Skin Graft in a Bald Eagle (Haliaeetus leucocephalus).
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- Journal of Avian Medicine & Surgery, 2019, v. 33, n. 2, p. 184, doi. 10.1647/2017-323
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- Publication type:
- Article
Complete Videoendoscopic Harvest And Transposition of Latissimus Dorsi Muscle for The Treatment of Poland Syndrome: A First Report.
- Published in:
- Journal of Laparoendoscopic & Advanced Surgical Techniques, 2007, v. 17, n. 1, p. 108, doi. 10.1089/lap.2006.0540
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- Publication type:
- Article
Unilateral syndactyly, hemihypertrophy, and hyperpigmentation with mosaic 2q35 deletion.
- Published in:
- Indian Journal of Dermatology, 2023, v. 68, n. 5, p. 558, doi. 10.4103/ijd.ijd_649_21
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- Publication type:
- Article