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 *

151 related articles for article (PubMed ID: 15633182)

  • 1. A new autosomal recessive oto-facial syndrome with midline malformations.
    Mégarbané A; Chouery E; Rassi S; Delague V
    Am J Med Genet A; 2005 Feb; 132A(4):398-401. PubMed ID: 15633182
    [TBL] [Abstract][Full Text] [Related]  

  • 2. New autosomal recessive syndrome with short stature and facio-auriculo-thoracic malformations.
    Mégarbané A; Daou L; Mégarbané H; Cave H; Chouery E; Verloes A
    Am J Med Genet A; 2004 Aug; 128A(4):414-7. PubMed ID: 15264289
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Anomalies of the auditory organ in Potter's syndrome. Histopathological findings in the temporal bone.
    Saito R; Takata N; Matsumoto N; Koide I; Fujita A; Ogura Y; Murakami M; Yanagida K; Komazawa M
    Arch Otolaryngol; 1982 Aug; 108(8):484-8. PubMed ID: 7103824
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cleft lip/palate, abnormal ears, ectrodactyly, congenital heart defect, and growth retardation: definition of the acro-cardio-facial syndrome.
    Guion-Almeida ML; Zechi-Ceide RM; Richieri-Costa A
    Clin Dysmorphol; 2000 Oct; 9(4):269-72. PubMed ID: 11045583
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: acro-fronto-facio-nasal dysostosis syndrome.
    Richieri-Costa A; Colletto GM; Gollop TR; Masiero D
    Am J Med Genet; 1985 Apr; 20(4):631-8. PubMed ID: 2986457
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Newly recognized autosomal recessive acrofacial dysostosis syndrome resembling Nager syndrome.
    Kennedy SJ; Teebi AS
    Am J Med Genet A; 2004 Aug; 129A(1):73-6. PubMed ID: 15266620
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A new dominant branchiogenic-deafness syndrome with internal auditory canal hypoplasia and abnormal extremities.
    Mégarbané A; Rassi S; Chouery E; Delague V; Perez de Nanclares Leal G; Tabet M; Castaño L; Loiselet J
    Am J Med Genet A; 2003 Jul; 120A(2):276-82. PubMed ID: 12833414
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Craniofacial morphology in the velo-cardio-facial syndrome.
    Arvystas M; Shprintzen RJ
    J Craniofac Genet Dev Biol; 1984; 4(1):39-45. PubMed ID: 6736220
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Auditory canal atresia, humeroscapular synostosis, and other skeletal abnormalities: confirmation of the autosomal recessive "SAMS" syndrome.
    ter Heide H; Bulstra SK; Reekers A; Schrander JJ; Schrander-Stumpel CT
    Am J Med Genet; 2002 Jul; 110(4):359-64. PubMed ID: 12116210
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Further case of aminopterin syndrome sine aminopterin in a Spanish child.
    Garcia-Minaur S; Botella MP
    Am J Med Genet; 2000 Dec; 95(4):320-4. PubMed ID: 11186884
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Oculo-oto-facial dysplasia (OOFD) versus Burn-McKeown syndrome.
    Wieczorek D; Gillessen-Kaesbach G
    Am J Med Genet A; 2006 Nov; 140(21):2381-2; author reply 2383-4. PubMed ID: 17022072
    [No Abstract]   [Full Text] [Related]  

  • 12. The Fryns syndrome: diaphragmatic defects, craniofacial dysmorphism, and distal digital hypoplasia. Further evidence for autosomal recessive inheritance.
    Meinecke P; Fryns JP
    Clin Genet; 1985 Dec; 28(6):516-20. PubMed ID: 4075561
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Newly recognized autosomal recessive faciothoracoskeletal syndrome.
    Richieri-Costa A; Guion-Almeida ML; Lauris JR; Ferreira DM
    Am J Med Genet; 1994 Jan; 49(2):224-8. PubMed ID: 8116673
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Oto-facial syndrome and esophageal atresia, intellectual disability and zygomatic anomalies - expanding the phenotypes associated with EFTUD2 mutations.
    Voigt C; Mégarbané A; Neveling K; Czeschik JC; Albrecht B; Callewaert B; von Deimling F; Hehr A; Falkenberg Smeland M; König R; Kuechler A; Marcelis C; Puiu M; Reardon W; Riise Stensland HM; Schweiger B; Steehouwer M; Teller C; Martin M; Rahmann S; Hehr U; Brunner HG; Lüdecke HJ; Wieczorek D
    Orphanet J Rare Dis; 2013 Jul; 8():110. PubMed ID: 23879989
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial syndrome of unusual triangular facies associated with cleft palate, malocclusion, midfacial hypoplasia and sensorineural hearing loss in two siblings. Is it a new autosomal recessive syndrome?
    Balcı S; Akcan B; Vargel İ; Tümer C; Enacar A
    Clin Dysmorphol; 2004 Apr; 13(2):71-74. PubMed ID: 15057120
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fryns syndrome: a new variable multiple congenital anomaly (MCA) syndrome.
    Lubinsky M; Severn C; Rapoport JM
    Am J Med Genet; 1983 Mar; 14(3):461-6. PubMed ID: 6859098
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dominantly inherited syndrome of microcephaly and cleft palate.
    Halal F
    Am J Med Genet; 1983 May; 15(1):135-40. PubMed ID: 6859112
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Temporal bone anomalies in the branchio-oto-renal syndrome: detailed computed tomographic and magnetic resonance imaging findings.
    Ceruti S; Stinckens C; Cremers CW; Casselman JW
    Otol Neurotol; 2002 Mar; 23(2):200-7. PubMed ID: 11875350
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Popliteal pterygium syndrome. Evidence for a severe autosomal recessive form.
    Bartsocas CS; Papas CV
    J Med Genet; 1972 Jun; 9(2):222-6. PubMed ID: 4339984
    [No Abstract]   [Full Text] [Related]  

  • 20. Peters'-Plus syndrome with agenesis of the corpus callosum: report of a case and confirmation of autosomal recessive inheritance.
    Camera G; Centa A; Pozzolo S; Camera A
    Clin Dysmorphol; 1993 Oct; 2(4):317-21. PubMed ID: 8305962
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.