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Journal Abstract Search

126 related items for PubMed ID: 3706402

  • 1. A genetic association between microcephaly and lymphedema.
    Crowe CA, Dickerman LH.
    Am J Med Genet; 1986 May; 24(1):131-5. PubMed ID: 3706402
    [Abstract] [Full Text] [Related]

  • 2. Microcephaly-lymphedema-chorioretinal dysplasia: a unique genetic syndrome with variable expression and possible characteristic facial appearance.
    Limwongse C, Wyszynski RE, Dickerman LH, Robin NH.
    Am J Med Genet; 1999 Sep 17; 86(3):215-8. PubMed ID: 10482868
    [Abstract] [Full Text] [Related]

  • 3. A genetic association between microcephaly and lymphedema.
    Meinecke P.
    Am J Med Genet; 1987 Jan 17; 26(1):233. PubMed ID: 3812570
    [No Abstract] [Full Text] [Related]

  • 4. Clinical variability in a Japanese hereditary lymphedema type I family with an FLT4 mutation.
    Mizuno S, Yamada Y, Yamada K, Nomura N, Wakamatsu N.
    Congenit Anom (Kyoto); 2005 Jun 17; 45(2):59-61. PubMed ID: 15904433
    [Abstract] [Full Text] [Related]

  • 5. Dominantly inherited syndrome of microcephaly and congenital lymphedema with normal intelligence.
    Leung AK.
    Am J Med Genet; 1987 Jan 17; 26(1):231. PubMed ID: 3812569
    [No Abstract] [Full Text] [Related]

  • 6. Dominantly inherited syndrome of microcephaly and congenital lymphedema.
    Leung AK.
    Clin Genet; 1985 Jun 17; 27(6):611-2. PubMed ID: 4017282
    [Abstract] [Full Text] [Related]

  • 7. Chorioretinal dysplasia-microcephaly-mental retardation syndrome: report of an American family.
    Sadler LS, Robinson LK.
    Am J Med Genet; 1993 Aug 01; 47(1):65-8. PubMed ID: 8368255
    [Abstract] [Full Text] [Related]

  • 8. Microcephaly, lymphedema, chorioretinopathy and atrial septal defect: a case report and review of the literature.
    Eventov-Friedman S, Singer A, Shinwell ES.
    Acta Paediatr; 2009 Apr 01; 98(4):758-9. PubMed ID: 19076985
    [Abstract] [Full Text] [Related]

  • 9. A syndrome of microcephaly and retinal pigmentary abnormalities without mental retardation in a family with coincidental autosomal dominant hyperreflexia.
    Parke JT, Riccardi VM, Lewis RA, Ferrell RE.
    Am J Med Genet; 1984 Mar 01; 17(3):585-94. PubMed ID: 6711609
    [Abstract] [Full Text] [Related]

  • 10. Evidence for genetic heterogeneity in lymphedema-cholestasis syndrome.
    Frühwirth M, Janecke AR, Müller T, Carlton VE, Kronenberg F, Offner F, Knisely AS, Geleff S, Song EJ, Simma B, Königsrainer A, Margreiter R, van der Hagen CB, Eiklid K, Aagenaes O, Bull L, Ellemunter H.
    J Pediatr; 2003 Apr 01; 142(4):441-7. PubMed ID: 12712065
    [Abstract] [Full Text] [Related]

  • 11. Congenital lymphedema in two siblings.
    Kajii T, Tsukahara M.
    Jinrui Idengaku Zasshi; 1985 Mar 01; 30(1):31-4. PubMed ID: 4010046
    [No Abstract] [Full Text] [Related]

  • 12. New syndrome: autosomal dominant microcephaly and radio-ulnar synostosis.
    Giuffrè L, Corsello G, Giuffrè M, Piccione M, Albanese A.
    Am J Med Genet; 1994 Jul 01; 51(3):266-9. PubMed ID: 8074157
    [Abstract] [Full Text] [Related]

  • 13. Microcephaly, lymphedema, and chorioretinal dysplasia: a distinct syndrome?
    Feingold M, Bartoshesky L.
    Am J Med Genet; 1992 Aug 01; 43(6):1030-1. PubMed ID: 1415329
    [Abstract] [Full Text] [Related]

  • 14. Distal aphalangia, syndactyly, and extra metatarsal, associated with short stature, microcephaly, and borderline intelligence: a new autosomal dominant disorder.
    Martínez-Frías ML, Martín M, Pardo M, Fernandez de las Heras F, Frías JL.
    Am J Med Genet; 1995 Jan 16; 55(2):213-6. PubMed ID: 7717420
    [Abstract] [Full Text] [Related]

  • 15. Microcephaly-lymphedema syndrome: report of a family with short stature as additional manifestation.
    Strenge S, Froster UG.
    Am J Med Genet; 1998 Dec 28; 80(5):506-9. PubMed ID: 9880217
    [Abstract] [Full Text] [Related]

  • 16. Autosomal dominant microcephaly--lymphoedema-chorioretinal dysplasia syndrome.
    Casteels I, Devriendt K, Van Cleynenbreugel H, Demaerel P, De Tavernier F, Fryns JP.
    Br J Ophthalmol; 2001 Apr 28; 85(4):499-500. PubMed ID: 11302131
    [No Abstract] [Full Text] [Related]

  • 17. [A case of congenital hereditary lymphedema (Milroy-Nonne's disease].
    Beluschi C, Coraiola M, Pedrotti D.
    Pediatr Med Chir; 1982 Apr 28; 4(1-2):155-7. PubMed ID: 7111035
    [No Abstract] [Full Text] [Related]

  • 18. [Ophthalmological findings in microcephaly-lymphoedema-chorioretinal dysplasia syndrome].
    Hatt Brupbacher SC, Job O, Senn P, Dedes W.
    Klin Monbl Augenheilkd; 2009 Apr 28; 226(4):344-6. PubMed ID: 19384796
    [Abstract] [Full Text] [Related]

  • 19. The Borjeson-Forssman-Lehmann syndrome. A family study.
    Dereymaeker AM, Fryns JP, Hoefnagels M, Heremans G, Marien J, van den Berghe H.
    Clin Genet; 1986 Apr 28; 29(4):317-20. PubMed ID: 3720009
    [Abstract] [Full Text] [Related]

  • 20. Microcephaly, lymphedema, and chorioretinal dysplasia: report of two additional cases.
    Angle B, Holgado S, Burton BK, Miller MT, Shapiro MJ, Opitz JM.
    Am J Med Genet; 1994 Nov 01; 53(2):99-101. PubMed ID: 7856652
    [Abstract] [Full Text] [Related]

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