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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

150 related items for PubMed ID: 5517969

  • 1. Limb abnormalities and mental retardation.
    Smith GF, Schindeler J, Elbualy S, Shear C.
    J Ment Defic Res; 1970 Dec; 14(4):319-41. PubMed ID: 5517969
    [No Abstract] [Full Text] [Related]

  • 2. Skeletal anomalies in genetically determined congenital heart disease.
    Poznanski AK, Stern AM, Gall JC.
    Radiol Clin North Am; 1971 Dec; 9(3):435-58. PubMed ID: 5145748
    [No Abstract] [Full Text] [Related]

  • 3. The thumb in the congenital malformation syndromes.
    Poznanski AK, Garn SM, Holt JF.
    Radiology; 1971 Jul; 100(1):115-29. PubMed ID: 5147019
    [No Abstract] [Full Text] [Related]

  • 4. A new syndrome with acrocephalopolysyndactyly, cardiac disease, and distinctive defects of the ear, skin, and lower limbs.
    Sakati N, Nyhan WL, Tisdale WK.
    J Pediatr; 1971 Jul; 79(1):104-9. PubMed ID: 4253694
    [No Abstract] [Full Text] [Related]

  • 5. Limb-heart syndrome.
    Joshi RM, Bharucha BA, Kumta NB, Vengsarkar AS.
    Indian Pediatr; 1985 May; 22(5):355-9. PubMed ID: 3833759
    [No Abstract] [Full Text] [Related]

  • 6. Letter: Apert syndrome does not equal mental retardation.
    Galli ML.
    J Pediatr; 1976 Oct; 89(4):691. PubMed ID: 957029
    [No Abstract] [Full Text] [Related]

  • 7. Genetics and malformations of the hand.
    Wynne-Davies R.
    Hand; 1971 Sep; 3(2):184-92. PubMed ID: 4331429
    [No Abstract] [Full Text] [Related]

  • 8. Reduction malformations and chromosome anomalies.
    Bofinger MK, Dignan PS, Schmidt RE, Warkany J.
    Am J Dis Child; 1973 Jan; 125(1):135-43. PubMed ID: 4346056
    [No Abstract] [Full Text] [Related]

  • 9. [Case of leprechaunism in a girl].
    Badalian LO, Petrukhin AS, Filina NP.
    Pediatriia; 1980 Dec; (12):24-7. PubMed ID: 7220166
    [No Abstract] [Full Text] [Related]

  • 10. Partial trisomy 22: a recognizable syndrome.
    Garlinger P, McGeary SA, Magenis E.
    Clin Genet; 1977 Jul; 12(1):9-16. PubMed ID: 891009
    [Abstract] [Full Text] [Related]

  • 11. [Clinical orofacial symptoms--guide to diagnosis of syndromes].
    Marković MD.
    Bilt Udruz Ortodonata Jugosl; 1990 Jul; 23(2):97-105. PubMed ID: 2151421
    [Abstract] [Full Text] [Related]

  • 12. Carpenter's syndrome: acrocephalopolysyndactyly. An autosomal recessive syndrome.
    Temtamy SA.
    J Pediatr; 1966 Jul; 69(1):111-20. PubMed ID: 5935752
    [No Abstract] [Full Text] [Related]

  • 13. Mesoectodermal dysplasia. A new combination of anomalies.
    Levy WJ.
    Am J Ophthalmol; 1967 May; 63(5):978-82. PubMed ID: 6066655
    [No Abstract] [Full Text] [Related]

  • 14. Trisomy 9 syndrome.
    Qazi QH, Masakawa A, Madahar C, Ehrlich R.
    Clin Genet; 1977 Oct; 12(4):221-6. PubMed ID: 912938
    [Abstract] [Full Text] [Related]

  • 15. Neurological disorders and growth disturbances in infancy and childhood.
    Gamstorp I.
    Eur Neurol; 1972 Oct; 7(1):1-25. PubMed ID: 4623050
    [No Abstract] [Full Text] [Related]

  • 16. Congenital malformation of the heart associated with congenital anomalies of the urinary tract, including a syndrome of ventricular septal defect, pulmonary hypertension, mental retardation, and skeletal deformity.
    MEHRIZI A.
    J Pediatr; 1962 Oct; 61():582-9. PubMed ID: 14472143
    [No Abstract] [Full Text] [Related]

  • 17. Upper limb-cardiovascular syndromes: a description of two new disorders with a classification.
    Tamari I, Goodman RM.
    Chest; 1974 Jun; 65(6):632-9. PubMed ID: 4275522
    [No Abstract] [Full Text] [Related]

  • 18. Trisomy in the distal end of the long arm of chromosome 3. A condition clinically similar to the Cornelia de Lange syndrome.
    Sciorra LJ, Bahng K, Lee ML.
    Am J Dis Child; 1979 Jul; 133(7):727-30. PubMed ID: 463821
    [Abstract] [Full Text] [Related]

  • 19. Sagittal craniostenosis, congenital heart disease, mental deficiency and various dysmorphies in two sibs--a "new" syndrome?
    Pfeiffer RA, Singer H, Zschiesche S.
    Eur J Pediatr; 1987 Jan; 146(1):75-8. PubMed ID: 3582410
    [Abstract] [Full Text] [Related]

  • 20. Unilateral limb and skin deformities with congenital heart disease in two siblings: a lethal syndrome.
    Falek A, Heath CW, Ebbin AJ, McLean WR.
    J Pediatr; 1968 Dec; 73(6):910-3. PubMed ID: 5696317
    [No Abstract] [Full Text] [Related]

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