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Pubmed for Handhelds

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Journal Abstract Search

234 related items for PubMed ID: 16396829

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  • 22. Two sibs with microcephaly, hygroma colli, renal dysplasia, and cutaneous syndactyly: a new lethal MCA syndrome?
    Janssen HC, Schaap C, Vandevijver N, Moerman P, de Die-Smulders CE, Fryns JP.
    J Med Genet; 1999 Jun; 36(6):481-4. PubMed ID: 10874639
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  • 27. Fraser syndrome in a 96-year-old female.
    Impallomeni M, Subramanian D, Mahmood N, Illes J.
    Age Ageing; 2006 Nov; 35(6):642-3. PubMed ID: 17047011
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  • 30. Fras1 deficiency results in cryptophthalmos, renal agenesis and blebbed phenotype in mice.
    Vrontou S, Petrou P, Meyer BI, Galanopoulos VK, Imai K, Yanagi M, Chowdhury K, Scambler PJ, Chalepakis G.
    Nat Genet; 2003 Jun; 34(2):209-14. PubMed ID: 12766770
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  • 33. Mortality and pathological findings in C (Opitz trigonocephaly) syndrome.
    Opitz JM, Putnam AR, Comstock JM, Chin S, Byrne JL, Kennedy A, Frikke MJ, Bernard C, Albrecht S, Der Kaloustian V, Szakacs JG.
    Fetal Pediatr Pathol; 2006 Jun; 25(4):211-31. PubMed ID: 17162528
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  • 36. Fraser syndrome with bladder pseudoexstrophy.
    Daia JA.
    Saudi Med J; 2001 May; 22(5):455-6. PubMed ID: 11376391
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  • 37. Mutchinick syndrome in a Japanese girl.
    Tonoki H, Hattori T, Kamoshida H, Ohta Y, Niikawa N.
    Am J Med Genet; 1999 Mar 12; 83(2):96-9. PubMed ID: 10190479
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  • 40. Bilateral anophthalmia and intrahepatic biliary atresia, two unusual components of Fraser syndrome: a case report.
    Brimo Alsaman MZ, Agha S, Sallah H, Badawi R, Kitaz MN, Assani A, Nawfal H.
    BMC Pregnancy Childbirth; 2020 Jun 10; 20(1):358. PubMed ID: 32522149
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