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Journal Abstract Search

102 related items for PubMed ID: 7332033

  • 1. Fronto-facio-nasal dysostosis - a new autosomal recessive syndrome.
    Gollop TR.
    Am J Med Genet; 1981; 10(4):409-12. PubMed ID: 7332033
    [No Abstract] [Full Text] [Related]

  • 2. 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; 20(4):631-8. PubMed ID: 2986457
    [Abstract] [Full Text] [Related]

  • 3. The Roberts syndrome.
    Freeman MV, Williams DW, Schimke RN, Temtamy SA, Vachier E, German J.
    Birth Defects Orig Artic Ser; 1974 Apr; 10(5):87-95. PubMed ID: 4220010
    [Abstract] [Full Text] [Related]

  • 4. Severe case of Al Awadi/Raas-Rothschild syndrome or new, possibly autosomal recessive facio-skeleto-genital syndrome.
    Mollica F, Mazzone D, Cimino G, Opitz JM.
    Am J Med Genet; 1995 Mar 27; 56(2):168-72. PubMed ID: 7625440
    [Abstract] [Full Text] [Related]

  • 5. Child with fronto-facio-nasal dysplasia, Hirschsprung's disease and hypospadias.
    Fryer AE.
    Clin Dysmorphol; 1993 Apr 27; 2(2):120-2. PubMed ID: 8281272
    [Abstract] [Full Text] [Related]

  • 6. Hypertelorism-microtia-clefting (HMC) syndrome.
    Verloes A.
    Genet Couns; 1994 Apr 27; 5(3):283-7. PubMed ID: 7811429
    [Abstract] [Full Text] [Related]

  • 7. Cleft lip and palate, characteristic facial appearance, malrotation of the intestine, and lethal congenital heart disease in two sibs: a new autosomal recessive condition?
    McPherson E, Clemens M.
    Am J Med Genet; 1996 Mar 01; 62(1):58-60. PubMed ID: 8779326
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  • 10. Autosomal recessive craniometaphyseal dysplasia.
    Penchaszadeh VB, Gutierrez ER, Figueroa E.
    Am J Med Genet; 1980 Mar 01; 5(1):43-55. PubMed ID: 7395899
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  • 11. Cleft lip and palate, hypertelorism, brachycephaly, flat facial profile, and congenital heart disease in three brothers.
    Nevin NC, Craig BG, Mullholland HC, Casey F.
    Am J Med Genet; 1997 Dec 31; 73(4):412-5. PubMed ID: 9415467
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  • 13. Setleis syndrome: autosomal recessive or autosomal dominant inheritance?
    al-Gazali LI, al-Talabani J.
    Clin Dysmorphol; 1996 Jul 31; 5(3):249-53. PubMed ID: 8818454
    [Abstract] [Full Text] [Related]

  • 14. Cerebellar hypoplasia, facial dysmorphism and internal abnormalities: a new recessive syndrome?
    Seller MJ, Pal K, Moscoso G, Nicolaides K, Hyett JA.
    Clin Dysmorphol; 1998 Jan 31; 7(1):41-4. PubMed ID: 9546829
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  • 17. Peters'-Plus syndrome with agenesis of the corpus callosum: report of a case and confirmation of autosomal recessive inheritance.
    Camera G, Centa A, Pozzolo S, Camera A.
    Clin Dysmorphol; 1993 Oct 31; 2(4):317-21. PubMed ID: 8305962
    [Abstract] [Full Text] [Related]

  • 18. Fryns syndrome.
    Stratton RF, Young RS, Heiman HS, Carter JM.
    Am J Med Genet; 1993 Mar 01; 45(5):562-4. PubMed ID: 8456824
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  • 19. Thomas syndrome: clinical variability and autosomal recessive inheritance.
    Briscioli V, Lalatta F, Rizzuti T, Fesslová V.
    Am J Med Genet; 1997 Aug 22; 71(3):373-4. PubMed ID: 9268113
    [No Abstract] [Full Text] [Related]

  • 20. [Robinow's syndrome in a family of consanguineous marriages].
    Gómez-Valencia L, Nájera-Martínez P.
    Bol Med Hosp Infant Mex; 1989 Apr 22; 46(4):303-4. PubMed ID: 2719815
    [No Abstract] [Full Text] [Related]

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