These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

142 related items for PubMed ID: 9768237

  • 1. [Craniofacial dysmorphism in pediatric AIDS. Presentation of a case].
    González Núñez I, Díaz Jidy M, Capó de Paz V, Rodríguez Barreras ME.
    Rev Cubana Med Trop; 1994; 46(1):60-4. PubMed ID: 9768237
    [Abstract] [Full Text] [Related]

  • 2. [Facial deformity associated with acquired immunodeficiency syndrome (AIDS). Report of two cases].
    Castillo Ariza M, Almonte Paulino R, Ariza Castillo F.
    Arch Domin Pediatr; 1988; 24(3):97-101. PubMed ID: 12343554
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Human T-cell lymphotropic virus type III (HTLV-III) embryopathy. A new dysmorphic syndrome associated with intrauterine HTLV-III infection.
    Marion RW, Wiznia AA, Hutcheon G, Rubinstein A.
    Am J Dis Child; 1986 Jul; 140(7):638-40. PubMed ID: 3012995
    [Abstract] [Full Text] [Related]

  • 5. [Congenital dwarfisms with dysmorphism. 1. Congenital dwarfism with craniofacial dysmorphism and body asymmetry (Silver-Russel type)].
    Anoussakis C, Karpathios T, Zervos N, Liakakos D.
    Pediatrie; 1974 Jul; 29(3):249-59. PubMed ID: 4438032
    [No Abstract] [Full Text] [Related]

  • 6. [The value of microcomputers in the diagnosis of craniofacial dysmorphism with multiple congenital abnormalities in children].
    Bijaoui G, Billette de Villemeur T.
    Arch Fr Pediatr; 1990 Jul; 47(6):468. PubMed ID: 2206109
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. New syndrome: mother and son with hypertelorism, downslanting palpebral fissures, malar hypoplasia, and apparently low-set ears associated with joint and scrotal anomalies.
    Seaver LH, Cassidy SB.
    Am J Med Genet; 1991 Dec 15; 41(4):405-9. PubMed ID: 1776627
    [Abstract] [Full Text] [Related]

  • 9. 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 15; 28(1):57-60. PubMed ID: 7400786
    [Abstract] [Full Text] [Related]

  • 10. [Congenital dwarfisms with dysmorphism. 2. Bird-head congenital dwarfism (Virchow-Seckel type)].
    Anoussakis C, Liakakos D, Zervos N, Karpathios T.
    Pediatrie; 1974 Mar 15; 29(3):261-7. PubMed ID: 4438033
    [No Abstract] [Full Text] [Related]

  • 11. Teebi hypertelorism syndrome: report of a third family.
    Toriello HV, Delp K.
    Clin Dysmorphol; 1994 Oct 15; 3(4):335-9. PubMed ID: 7894738
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. [Anesthesia-reanimation for surgery of cranio-facial dysmorphism. Apropos of 23 cases of remodeling of the forehead].
    Domblides N, Lorelle D, Mehsen M, Marguinaud E, Besse JL, Boulard G.
    Minerva Anestesiol; 1989 Apr 15; 55(4):161-4. PubMed ID: 2615986
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. [The r(14) syndrome. 3 new observations].
    Gilgenkrantz S, Morali A, Vidailhet M, Saura R, Serville F, Fontan D, Moraine C.
    Ann Genet; 1984 Apr 15; 27(2):73-8. PubMed ID: 6431894
    [Abstract] [Full Text] [Related]

  • 17. [Gigantism with encephalopathy and craniofacial dysmorphism].
    Marie J, Royer P, Lévèque B, Debauchez C, Rappaport R.
    Ann Pediatr (Paris); 1965 Nov 02; 12(11):682-91. PubMed ID: 5851848
    [No Abstract] [Full Text] [Related]

  • 18. More on human immunodeficiency virus embryopathy.
    Iosub S, Bamji M, Stone RK, Gromisch DS, Wasserman E.
    Pediatrics; 1987 Oct 02; 80(4):512-6. PubMed ID: 3658569
    [Abstract] [Full Text] [Related]

  • 19. Dysmorphic growth and development and the study of craniofacial syndromes.
    Cohen MM.
    J Craniofac Genet Dev Biol Suppl; 1985 Oct 02; 1():43-55. PubMed ID: 3877108
    [Abstract] [Full Text] [Related]

  • 20. A de novo 7.6Mb tandem duplication of 14q32.2-qter associated with primordial short stature with neurosecretory growth hormone dysfunction, distinct facial anomalies and mild developmental delay.
    Thiel CT, Dörr HG, Trautmann U, Hoyer J, Hofmann K, Kraus C, Ekici AB, Reis A, Rauch A.
    Eur J Med Genet; 2008 Oct 02; 51(4):362-7. PubMed ID: 18434272
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.