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Journal Abstract Search

115 related items for PubMed ID: 7081301

  • 1. A review and case report of aprosencephaly and the XK aprosencephaly syndrome.
    Martin RA, Carey JG.
    Am J Med Genet; 1982 Mar; 11(3):369-71. PubMed ID: 7081301
    [No Abstract] [Full Text] [Related]

  • 2. XK aprosencephaly and anencephaly in sibs.
    Townes PL, Reuter K, Rosquete EE, Magee BD.
    Am J Med Genet; 1988 Mar; 29(3):523-8. PubMed ID: 3287923
    [Abstract] [Full Text] [Related]

  • 3. Atelencephalic aprosencephaly.
    Harris CP, Townsend JJ, Norman MG, White VA, Viskochil DH, Pysher TJ, Klatt EC.
    J Child Neurol; 1994 Oct; 9(4):412-6. PubMed ID: 7822735
    [Abstract] [Full Text] [Related]

  • 4. Mosaic r(13) in an infant with aprosencephaly.
    Goldsmith CL, Tawagi GF, Carpenter BF, Speevak MD, Hunter AG.
    Am J Med Genet; 1993 Sep 15; 47(4):531-3. PubMed ID: 8256818
    [Abstract] [Full Text] [Related]

  • 5. [On an unusual case of multiple congenital malformations].
    Cela G.
    Minerva Pediatr; 1966 Sep 22; 18(27):1500-5. PubMed ID: 5994491
    [No Abstract] [Full Text] [Related]

  • 6. Acephalus acardiac fetus.
    Rajesh B, Mahadhevan B, Rao S, Bhat VB.
    Indian J Pediatr; 2004 Oct 22; 71(10):948. PubMed ID: 15531853
    [Abstract] [Full Text] [Related]

  • 7. Brief clinical reports: aprosencephaly-atelencephaly and the aprosencephaly (XK) syndrome.
    Lurie IW, Nedzved MK, Lazjuk GI, Kirillova IA, Cherstvoy ED.
    Am J Med Genet; 1979 Oct 22; 3(3):301-9. PubMed ID: 114053
    [Abstract] [Full Text] [Related]

  • 8. Anencephaly and limb deficiencies.
    Rodríguez JI, Rodríguez-Peralto JL, Muro M, Urioste M, Palacios J.
    Am J Med Genet; 1992 Sep 01; 44(1):66-71. PubMed ID: 1519654
    [Abstract] [Full Text] [Related]

  • 9. Anomalies of the forebrain with radial limb defects: Garcia-Lurie-Steinfeld syndrome?
    McPherson E, Huff D, Dunn J, Muenke M.
    Birth Defects Res A Clin Mol Teratol; 2004 Aug 01; 70(8):537-44. PubMed ID: 15329833
    [Abstract] [Full Text] [Related]

  • 10. [Low cholesterol and pathological manifestations: Smith-Lemli-Opitz syndrome].
    Franceschini P, Franceschini D.
    Minerva Pediatr; 1994 Dec 01; 46(12):579-80. PubMed ID: 7731422
    [No Abstract] [Full Text] [Related]

  • 11. [The etiopathogenesis of congenital multiple malformations].
    D'Addato F, Visentin L, Surico N.
    Minerva Ginecol; 1979 Sep 01; 31(9):639-44. PubMed ID: 43957
    [No Abstract] [Full Text] [Related]

  • 12. The XK-aprosencephaly syndrome.
    Lurie IW, Nedzed MK, Lazjuk GI, Kirillova IA, Cherstvoy ED, Ostrovskaja TI, Shved IA.
    Am J Med Genet; 1980 Sep 01; 7(2):231-4. PubMed ID: 7193413
    [No Abstract] [Full Text] [Related]

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  • 15. [Trisomy 18 syndrome(Edwards syndrome)].
    Ieshima A.
    Ryoikibetsu Shokogun Shirizu; 2000 Sep 01; (30 Pt 5):340-1. PubMed ID: 11057253
    [No Abstract] [Full Text] [Related]

  • 16. [Triploidy syndrome and diploid/triploid mixoploidy syndrome].
    Kato R.
    Ryoikibetsu Shokogun Shirizu; 2000 Sep 01; (30 Pt 5):361-2. PubMed ID: 11057261
    [No Abstract] [Full Text] [Related]

  • 17. Anencephaly: a review.
    Nakano KK.
    Dev Med Child Neurol; 1973 Jun 01; 15(3):383-400. PubMed ID: 4591551
    [No Abstract] [Full Text] [Related]

  • 18. Anencephaly: a review.
    Nakano KK.
    Arkh Anat Gistol Embriol; 1972 Aug 01; 63(8):383-400. PubMed ID: 4580449
    [No Abstract] [Full Text] [Related]

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  • 20. Diaphragmatic defects, craniofacial dysmorphism, cleft palate and distal limb deformities. - a new lethal syndrome.
    Goddeeris P, Fryns JP, van den Berghe H.
    J Genet Hum; 1980 Mar 01; 28(1):57-60. PubMed ID: 7400786
    [Abstract] [Full Text] [Related]

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