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Journal Abstract Search

149 related items for PubMed ID: 15636261

  • 21.
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  • 22. [Cohen syndrome. Personal case report and literature review].
    Oztürk B, Weber HP.
    Monatsschr Kinderheilkd; 1991 Dec; 139(12):844-8. PubMed ID: 1770962
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  • 25. Genitourinary anomalies of pediatric FG syndrome.
    Smith JF, Wayment RO, Cartwright PC, Snow BW, Opitz JM.
    J Urol; 2007 Aug; 178(2):656-9. PubMed ID: 17574621
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  • 32. A second patient with MCA/MR syndrome with multiple circumferential skin creases.
    Leonard NJ.
    Am J Med Genet; 2002 Sep 15; 112(1):91-4. PubMed ID: 12239728
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  • 33. MORM syndrome (mental retardation, truncal obesity, retinal dystrophy and micropenis), a new autosomal recessive disorder, links to 9q34.
    Hampshire DJ, Ayub M, Springell K, Roberts E, Jafri H, Rashid Y, Bond J, Riley JH, Woods CG.
    Eur J Hum Genet; 2006 May 15; 14(5):543-8. PubMed ID: 16493448
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  • 34.
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  • 35. Cohen syndrome.
    Alavi S, Kher A, Kumar A, Muranjan M, Bharucha B.
    Indian Pediatr; 1993 May 15; 30(5):678-81. PubMed ID: 8282400
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  • 36. Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndrome.
    Lyons MJ, Graham JM, Neri G, Hunter AG, Clark RD, Rogers RC, Moscarda M, Boccuto L, Simensen R, Dodd J, Robertson S, DuPont BR, Friez MJ, Schwartz CE, Stevenson RE.
    J Med Genet; 2009 Jan 15; 46(1):9-13. PubMed ID: 18805826
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  • 37. [Kabuki syndrome in the differential diagnosis of neonatal hypotonia].
    Aguilera Albesa S, Botella Astorqui MP, Ocio Ocio I.
    An Pediatr (Barc); 2009 Jan 15; 70(1):91-3. PubMed ID: 19174128
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  • 39. MRI of the brain in muscle-eye-brain (MEB) disease.
    Valanne L, Pihko H, Katevuo K, Karttunen P, Somer H, Santavuori P.
    Neuroradiology; 1994 Aug 15; 36(6):473-6. PubMed ID: 7991095
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  • 40. [Variability of clinical manifestations in the family with Axenfeld-Rieger syndrome].
    Kamińska A, Sokołowska-Oracz A, Pawluczyk-Dyjecińska M, Szaflik JP.
    Klin Oczna; 2007 Aug 15; 109(7-9):321-6. PubMed ID: 18260289
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