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Journal Abstract Search

123 related items for PubMed ID: 3034618

  • 1. An unusual, possibly "new" MA/MR syndrome with sagittal craniosynostosis.
    Pfeiffer RA, Tietze U, Welte W.
    Eur J Pediatr; 1987 Jan; 146(1):74-5. PubMed ID: 3034618
    [Abstract] [Full Text] [Related]

  • 2. Sagittal craniostenosis, congenital heart disease, mental deficiency and various dysmorphies in two sibs--a "new" syndrome?
    Pfeiffer RA, Singer H, Zschiesche S.
    Eur J Pediatr; 1987 Jan; 146(1):75-8. PubMed ID: 3582410
    [Abstract] [Full Text] [Related]

  • 3. Congenital heart disease in an infant with the Smith-Lemli-Opitz syndrome.
    Park SC, Needles CF, Dimich I, Sussman L.
    J Pediatr; 1968 Dec; 73(6):896-902. PubMed ID: 4386913
    [No Abstract] [Full Text] [Related]

  • 4. Associated acral and renal malformations: a new syndrome?
    Curran AS, Curran JP.
    Pediatrics; 1972 May; 49(5):716-25. PubMed ID: 4402497
    [No Abstract] [Full Text] [Related]

  • 5. Kleeblattschädel syndrome.
    Rosenbaum KN, Weisskopf B.
    J Ky Med Assoc; 1971 Aug; 69(8):594-7. PubMed ID: 4327692
    [No Abstract] [Full Text] [Related]

  • 6. Congenital ocular anomalies in 800 mentally deficient patients.
    Falbe-Hansen I.
    Acta Ophthalmol (Copenh); 1968 Aug; 46(3):391-7. PubMed ID: 4303604
    [No Abstract] [Full Text] [Related]

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  • 9. [Syndrome of craniosynostosis with syn- or polydactylia].
    Lorenz P, Hinkel GK, Rupprecht E.
    Kinderarztl Prax; 1991 Aug; 59(7-8):195-9. PubMed ID: 1656132
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  • 12. Unusual cranial deformities and associated anomalies in defective persons.
    LOKEY J.
    N C Med J; 1956 May; 17(5):223-5. PubMed ID: 13322311
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  • 15. Congenital bilateral fibular deficiency with facial dysmorphia, brachydactyly and mental retardation in a girl.
    Stoll C, Alembik Y, Repetto M.
    Genet Couns; 1998 May; 9(2):147-52. PubMed ID: 9664212
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