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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

141 related items for PubMed ID: 1606716

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  • 3. Dandy-Walker(like) malformation, atrio-ventricular septal defect and a similar pattern of minor anomalies in 2 sisters: a new syndrome?
    Ritscher D, Schinzel A, Boltshauser E, Briner J, Arbenz U, Sigg P.
    Am J Med Genet; 1987 Feb; 26(2):481-91. PubMed ID: 3812597
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  • 5. Ritscher-Schinzel (3C) syndrome: documentation of the phenotype.
    Kosaki K, Curry CJ, Roeder E, Jones KL.
    Am J Med Genet; 1997 Feb 11; 68(4):421-7. PubMed ID: 9021015
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  • 8. Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.
    Leonardi ML, Pai GS, Wilkes B, Lebel RR.
    Am J Med Genet; 2001 Aug 15; 102(3):237-42. PubMed ID: 11484200
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  • 9. The Aase-Smith syndrome.
    Patton MA, Sharma A, Winter RM.
    Clin Genet; 1985 Dec 15; 28(6):521-5. PubMed ID: 4075562
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  • 11. A new lethal chondrodysplasia with spondylocostal dysostosis, multiple internal anomalies and Dandy-Walker cyst.
    Moerman P, Vandenberghe K, Fryns JP, Haspeslagh M, Lauweryns JM.
    Clin Genet; 1985 Feb 15; 27(2):160-4. PubMed ID: 3884191
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  • 12. Congenital cutis laxa with ligamentous laxity and delayed development, Dandy-Walker malformation and minor heart and osseous defects.
    Biver A, De Rijcke S, Toppet V, Ledoux-Corbusier M, Van Maldergem L.
    Clin Genet; 1994 Jun 15; 45(6):318-22. PubMed ID: 7523003
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  • 17. Sagittal craniosynostosis, Dandy-Walker malformation, and hydrocephalus: a unique multiple malformation syndrome.
    Braddock SR, Jones KL, Superneau DW, Jones MC.
    Am J Med Genet; 1993 Oct 01; 47(5):640-3; discussion 644. PubMed ID: 8266990
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  • 18. Velocardiofacial syndrome in a mother and daughter: variability of the clinical phenotype.
    Holder SE, Winter RM, Kamath S, Scambler PJ.
    J Med Genet; 1993 Oct 01; 30(10):825-7. PubMed ID: 8230158
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