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Journal Abstract Search

111 related items for PubMed ID: 837627

  • 1. Cockayne syndrome.
    Johnson CF.
    Clin Pediatr (Phila); 1977 Mar; 16(3):232. PubMed ID: 837627
    [No Abstract] [Full Text] [Related]

  • 2. Cockayne syndrome: clinical study of two patients and neuropathologic findings in one.
    Sugarman GI, Landing BH, Reed WB.
    Clin Pediatr (Phila); 1977 Mar; 16(3):225-32. PubMed ID: 837626
    [No Abstract] [Full Text] [Related]

  • 3. Tapetoretinal degeneration and mental retardation associated with microspherophakia and mesodermal abnormalities: a new syndrome?
    Sierpinski-Bart J, Neumann E, Tirosh E, Atias D.
    Metab Pediatr Ophthalmol; 1981 Mar; 5(3-4):225-31. PubMed ID: 6273671
    [No Abstract] [Full Text] [Related]

  • 4. A new syndrome of dwarfism, brachydactyly, nail dysplasia, and mental retardation in sibs.
    Tonoki H, Kishino T, Niikawa N.
    Am J Med Genet; 1990 May; 36(1):89-93. PubMed ID: 2333912
    [Abstract] [Full Text] [Related]

  • 5. A newly recognized inherited syndrome of dwarfism, craniosynostosis, retinitis pigmentosa and multiple congenital malformations.
    Armendares S, Antillón F, del Castillo V, Jiménez M.
    Birth Defects Orig Artic Ser; 1975 May; 11(5):49-53. PubMed ID: 1218234
    [No Abstract] [Full Text] [Related]

  • 6. The Dubowitz syndrome--one more case.
    Chrzanowska KH, Krajewska-Walasek M.
    Klin Padiatr; 1987 May; 199(5):370-2. PubMed ID: 3316825
    [Abstract] [Full Text] [Related]

  • 7. X-linked mental retardation, microcephaly, and growth delay associated with hereditary bullous dystrophy macular type: report of a second family.
    Lungarotti MS, Martello C, Barboni G, Mezzetti D, Mariotti G, Calabro A.
    Am J Med Genet; 1994 Jul 15; 51(4):598-601. PubMed ID: 7943046
    [Abstract] [Full Text] [Related]

  • 8. Brachytelephalangy with mental retardation, peculiar face and short stature in two sibs. A new MCA/MR syndrome?
    Mégarbané A, Abi Moussa M.
    Genet Couns; 1997 Jul 15; 8(2):127-32. PubMed ID: 9219011
    [Abstract] [Full Text] [Related]

  • 9. [Dubowitz syndrome. A diagnosis not to be missed].
    Mathieu M, Berquin P, Epelbaum S, Lenaerts C, Piussan C.
    Arch Fr Pediatr; 1991 Dec 15; 48(10):715-8. PubMed ID: 1793348
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Pigmentary retinopathy, hearing loss, mental retardation, and dysmorphism in sibs: a new syndrome?
    Hersh JH, Podruch PE, Weisskopf B.
    Birth Defects Orig Artic Ser; 1982 Jan 16; 18(3B):175-82. PubMed ID: 7139098
    [No Abstract] [Full Text] [Related]

  • 12. Cleft palate-lateral synechiae syndrome: report on three new patients with additional findings and evidence for variability and heterogeneity.
    Nakata NM, Guion-Almeida ML, Richieri-Costa A.
    Am J Med Genet; 1993 Sep 01; 47(3):330-2. PubMed ID: 8135276
    [Abstract] [Full Text] [Related]

  • 13. [Cardiac symptoms in 2 patients with Seckel syndrome].
    Rappen U, von Brenndorff AI.
    Monatsschr Kinderheilkd; 1993 Jul 01; 141(7):584-6. PubMed ID: 8413337
    [Abstract] [Full Text] [Related]

  • 14. Chorioretinal dysplasia-microcephaly-mental retardation syndrome.
    Warburg M, Heuer HE.
    Am J Med Genet; 1994 Aug 01; 52(1):117. PubMed ID: 7977454
    [No Abstract] [Full Text] [Related]

  • 15. [An unusual picture of pigmentary dermatologic disease associated with retinitis pigmentosa, cataract and congenital deafness, oligophrenia and cerebellar ataxia].
    Scialdone D, Artifoni E.
    G Ital Oftalmol; 1964 Aug 01; 17(1):49-60. PubMed ID: 5827882
    [No Abstract] [Full Text] [Related]

  • 16. Optic atrophy, microcephaly, mental retardation and mosaic variegated aneuploidy: a human mitotic mutation.
    Bitoun P, Martin-Pont B, Tamboise E, Gaudelus J.
    Ann Genet; 1994 Aug 01; 37(2):75-7. PubMed ID: 7985982
    [Abstract] [Full Text] [Related]

  • 17. Microcephaly and digital anomalies: a newly recognized syndrome of recessively inherited mental retardation.
    Kelly TE, Kirson L, Wyatt J.
    Am J Med Genet; 1993 Feb 01; 45(3):353-5. PubMed ID: 8434622
    [Abstract] [Full Text] [Related]

  • 18. Short stature, mental retardation and multiple dysmorphisms in two unrelated females: one or two different syndromes or none?
    Pfeiffer RA, Kapferer L, Tietze HU.
    Genet Couns; 1996 Feb 01; 7(3):213-7. PubMed ID: 8897043
    [Abstract] [Full Text] [Related]

  • 19. Dwarfism associated with borderline intelligence, microcephaly, microphthalmia, and vertebral anomalies.
    Barber ND, Say B, Coldwell JG.
    Birth Defects Orig Artic Ser; 1979 Feb 01; 15(5B):355-60. PubMed ID: 526589
    [No Abstract] [Full Text] [Related]

  • 20. [Cohen syndrome].
    Kayashima T, Niikawa N.
    Ryoikibetsu Shokogun Shirizu; 2001 Feb 01; (36):477-8. PubMed ID: 11596442
    [No Abstract] [Full Text] [Related]

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