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Journal Abstract Search

363 related items for PubMed ID: 2624276

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  • 3. Severe lymphedema, intestinal lymphangiectasia, seizures and mild mental retardation: further case of Hennekam syndrome with a severe phenotype.
    Forzano F, Faravelli F, Loy A, Di Rocco M.
    Am J Med Genet; 2002 Jul 22; 111(1):68-70. PubMed ID: 12124738
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  • 4. Intestinal lymphangiectasia, lymphedema, mental retardation, and typical face: confirmation of the Hennekam syndrome.
    Gabrielli O, Catassi C, Carlucci A, Coppa GV, Giorgi P.
    Am J Med Genet; 1991 Aug 01; 40(2):244-7. PubMed ID: 1897580
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  • 5. Lymphedema-lymphangiectasia-mental retardation (Hennekam) syndrome: a review.
    Van Balkom ID, Alders M, Allanson J, Bellini C, Frank U, De Jong G, Kolbe I, Lacombe D, Rockson S, Rowe P, Wijburg F, Hennekam RC.
    Am J Med Genet; 2002 Nov 01; 112(4):412-21. PubMed ID: 12376947
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  • 6. Familial congenital pulmonary lymphangectasia, non-immune hydrops fetalis, facial and lower limb lymphedema: confirmation of Njolstad's report.
    Jacquemont S, Barbarot S, Bocéno M, Stalder JF, David A.
    Am J Med Genet; 2000 Aug 14; 93(4):264-8. PubMed ID: 10946350
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  • 8. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome?
    Bindewald B, Ulmer H, Müller U.
    Am J Med Genet; 1994 Apr 01; 50(2):173-6. PubMed ID: 8010348
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  • 9. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with growth failure, lip/palate cleft(s), and urogenital anomalies.
    Malpuech G, Demeocq F, Palcoux JB, Vanlieferinghen P.
    Am J Med Genet; 1983 Dec 01; 16(4):475-80. PubMed ID: 6660246
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  • 11. Multicore disease in sibs with severe mental retardation, short stature, facial anomalies, hypoplasia of the pituitary fossa, and hypogonadotrophic hypogonadism.
    Chudley AE, Rozdilsky B, Houston CS, Becker LE, Knoll JH.
    Am J Med Genet; 1985 Jan 01; 20(1):145-58. PubMed ID: 3970066
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  • 12. 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 01; 20(4):631-8. PubMed ID: 2986457
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  • 13. Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibs.
    Chitayat D, Hall JG, Couch RM, Phang MS, Baldwin VJ.
    Am J Med Genet; 1990 Sep 01; 37(1):65-70. PubMed ID: 2240046
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  • 17. [A case of Hennekam syndrome presenting with massive pericardial effusion].
    Nişli K, Oner N, Kayserili H, Ertuğrul T.
    Turk Kardiyol Dern Ars; 2008 Jul 01; 36(5):325-8. PubMed ID: 18984984
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  • 18. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.
    Bonioli E, Palmieri A, Bertola A, Bellini C.
    Genet Couns; 1995 Jul 01; 6(4):309-12. PubMed ID: 8775417
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