These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 16761296)

  • 101. Clinical and cytogenomic findings in OAV spectrum.
    Bragagnolo S; Colovati MES; Souza MZ; Dantas AG; F de Soares MF; Melaragno MI; Perez AB
    Am J Med Genet A; 2018 Mar; 176(3):638-648. PubMed ID: 29368383
    [TBL] [Abstract][Full Text] [Related]  

  • 102.
    Celse T; Tingaud-Sequeira A; Dieterich K; Siegfried G; Lecaignec C; Bouneau L; Fannemel M; Salaun G; Laffargue F; Martinez G; Satre V; Vieville G; Bidart M; Soussi Zander C; Turesson AC; Splitt M; Reboul D; Chiesa J; Khau Van Kien P; Godin M; Gruchy N; Goel H; Palmer E; Demetriou K; Shalhoub C; Rooryck C; Coutton C
    J Med Genet; 2023 Jun; 60(6):620-626. PubMed ID: 36368868
    [TBL] [Abstract][Full Text] [Related]  

  • 103. Severe nasomaxillary hypoplasia (Binder phenotype) on prenatal US/MRI: an important marker for the prenatal diagnosis of chondrodysplasia punctata.
    Blask AR; Rubio EI; Chapman KA; Lawrence AK; Bulas DI
    Pediatr Radiol; 2018 Jul; 48(7):979-991. PubMed ID: 29572747
    [TBL] [Abstract][Full Text] [Related]  

  • 104. Goldenhar Syndrome - ophthalmologist's perspective.
    Schmitzer S; Burcel M; Dăscălescu D; Popteanu IC
    Rom J Ophthalmol; 2018; 62(2):96-104. PubMed ID: 30206552
    [TBL] [Abstract][Full Text] [Related]  

  • 105. Oculo-auriculo-vertebral complex and uncommon associated anomalies: report on 8 unrelated Brazilian patients.
    van Bever Y; van den Ende JJ; Richieri-Costa A
    Am J Med Genet; 1992 Nov; 44(5):683-90. PubMed ID: 1481833
    [TBL] [Abstract][Full Text] [Related]  

  • 106. Abnormal soft palate movements in patients with microtia.
    Kolodzynski MN; van Hoorn BT; Kon M; Breugem CC
    J Plast Reconstr Aesthet Surg; 2018 Oct; 71(10):1476-1480. PubMed ID: 30001915
    [TBL] [Abstract][Full Text] [Related]  

  • 107. Oculo-auriculo-vertebral spectrum.
    Schaefer GB; Olney AH; Kolodziej P
    Ear Nose Throat J; 1998 Jan; 77(1):17-8. PubMed ID: 9473828
    [No Abstract]   [Full Text] [Related]  

  • 108. Goldenhar syndrome (oculoauriculovertebral dysplasia): report of one case.
    Ng YY; Hu JM; Su PH; Chen JY; Yang MS; Chen SJ
    Acta Paediatr Taiwan; 2006; 47(3):142-5. PubMed ID: 17078468
    [TBL] [Abstract][Full Text] [Related]  

  • 109. Discordance for skeletal and cardiac defect in monozygotic twins.
    Stoll C; Roth MP; Dott B; Bigel P
    Acta Genet Med Gemellol (Roma); 1984; 33(3):501-4. PubMed ID: 6543281
    [TBL] [Abstract][Full Text] [Related]  

  • 110. Severe oculocerebrocutaneous (Delleman) syndrome: overlap with Goldenhar anomaly.
    McCandless SE; Robin NH
    Am J Med Genet; 1998 Jul; 78(3):282-5. PubMed ID: 9677067
    [TBL] [Abstract][Full Text] [Related]  

  • 111. Three-generation family with resemblance to Townes-Brocks syndrome and Goldenhar/oculoauriculovertebral spectrum.
    Johnson JP; Poskanzer LS; Sherman S
    Am J Med Genet; 1996 Jan; 61(2):134-9. PubMed ID: 8669439
    [TBL] [Abstract][Full Text] [Related]  

  • 112. Ectopic external auditory canal and ossicular formation in the oculo-auriculo-vertebral spectrum.
    Supakul N; Kralik SF; Ho CY
    Pediatr Radiol; 2015 Jul; 45(7):1099-102. PubMed ID: 25480433
    [TBL] [Abstract][Full Text] [Related]  

  • 113. Hemifacial Microsomia : Clinicoradiological Insight and Report of a Case.
    Chhabra N; Chhabra A
    Ethiop J Health Sci; 2017 Jan; 27(1):91-94. PubMed ID: 28458495
    [TBL] [Abstract][Full Text] [Related]  

  • 114. Mutations in
    Lopez E; Berenguer M; Tingaud-Sequeira A; Marlin S; Toutain A; Denoyelle F; Picard A; Charron S; Mathieu G; de Belvalet H; Arveiler B; Babin PJ; Lacombe D; Rooryck C
    J Med Genet; 2016 Nov; 53(11):752-760. PubMed ID: 27358179
    [TBL] [Abstract][Full Text] [Related]  

  • 115. Non-overlapping 22q11.2 microdeletions in patients with oculo-auriculo-vertebral spectrum.
    Dos Santos PA; de Oliveira SF; Freitas EL; Safatle HP; Rosenberg C; Ferrari I; Mazzeu JF
    Am J Med Genet A; 2014 Feb; 164A(2):551-3. PubMed ID: 24311469
    [No Abstract]   [Full Text] [Related]  

  • 116. GLI2 mutations in four Brazilian patients: how wide is the phenotypic spectrum?
    Rahimov F; Ribeiro LA; de Miranda E; Richieri-Costa A; Murray JC
    Am J Med Genet A; 2006 Dec; 140(23):2571-6. PubMed ID: 17096318
    [TBL] [Abstract][Full Text] [Related]  

  • 117. Oculo auriculo vertebral spectrum and CHARGE association.
    Bathula S; Bhate M
    BMJ Case Rep; 2023 Apr; 16(4):. PubMed ID: 37068843
    [TBL] [Abstract][Full Text] [Related]  

  • 118. Craniofacial and airway morphology of individuals with oculoauriculovertebral spectrum.
    Parizotto JOL; Peixoto AP; Borsato KT; Bianchi J; Vendramini Pittoli S; Tonello C; Gonçalves JR
    Orthod Craniofac Res; 2021 Nov; 24(4):575-584. PubMed ID: 33713375
    [TBL] [Abstract][Full Text] [Related]  

  • 119. Severe fatal course of axial mesodermal dysplasia spectrum associated with complex cardiac defect in an infant of a mother with insulin dependent diabetes.
    Dinleyici EC; Tekin N; Dinleyici M; Kilic Z; Adapinar B; Aksit MA
    Am J Med Genet A; 2007 Sep; 143A(18):2156-9. PubMed ID: 17676608
    [TBL] [Abstract][Full Text] [Related]  

  • 120. 45,X/46,XY mosaicism and Oculo-Auriculo-Vertebral Spectrum following an IVF pregnancy: a report and a discussion of their interrelationships.
    Baynam G; Goldblatt J
    J Maxillofac Oral Surg; 2009 Sep; 8(3):279-82. PubMed ID: 23139526
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.