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Journal Abstract Search

132 related items for PubMed ID: 11102922

  • 41. [Oto-palato-digital type I syndrome in five generations. Relationship to the type II form].
    Le Marec B, Odent S, Bracq E, Bulard MB, Bourdinière J, Babut JM.
    Ann Genet; 1988; 31(3):155-61. PubMed ID: 3265608
    [Abstract] [Full Text] [Related]

  • 42. Anetoderma in a patient with terminal osseous dysplasia with pigmentary defects.
    Connor CJ, Shchelochkov OA, Ciliberto H.
    Am J Med Genet A; 2015 Oct; 167A(10):2459-62. PubMed ID: 26059211
    [Abstract] [Full Text] [Related]

  • 43. Osteochondrodysplasia in Fryns syndrome.
    Kershisnik MM, Craven CM, Jung AL, Carey JC, Knisely AS.
    Am J Dis Child; 1991 Jun; 145(6):656-60. PubMed ID: 1903587
    [Abstract] [Full Text] [Related]

  • 44. Metaphyseal anadysplasia type II: a new regressive metaphyseal dysplasia.
    Le Merrer M, Maroteaux P.
    Pediatr Radiol; 1998 Oct; 28(10):771-5. PubMed ID: 9799299
    [Abstract] [Full Text] [Related]

  • 45. Otopalatodigital syndrome type II associated with omphalocele: report of three cases.
    Young K, Barth CK, Moore C, Weaver DD.
    Am J Med Genet; 1993 Feb 15; 45(4):481-7. PubMed ID: 8465856
    [Abstract] [Full Text] [Related]

  • 46. A variant of Cenani-Lenz type syndactyly.
    Seven M, Yüksel A, Ozkiliç A, Elçioğlu N.
    Genet Couns; 2000 Feb 15; 11(1):41-7. PubMed ID: 10756427
    [Abstract] [Full Text] [Related]

  • 47. Cerebro-osseous-digital syndrome: four new cases of a lethal skeletal dysplasia--distinct from Neu-Laxova Syndrome.
    Elliott AM, Gonzales M, Hoeffel JC, Le Merrer M, Maroteaux P, Encha-Razavi F, Joye N, Berchel C, Fliegel C, Aughton DJ, Beaudry-Rodgers K, Hasteh F, Nerlich AG, Wilcox WR, Rimoin DL, Lachman RS, Freisinger P.
    Am J Med Genet; 2002 Apr 22; 109(2):139-48. PubMed ID: 11977163
    [Abstract] [Full Text] [Related]

  • 48. Oto-palato-digital syndrome type II. Report of two related cases.
    Gendall PW, Kozlowski K.
    Pediatr Radiol; 1992 Apr 22; 22(4):267-9. PubMed ID: 1523048
    [Abstract] [Full Text] [Related]

  • 49. Gracile bone dysplasia.
    Thomas JA, Rimoin DL, Lachman RS, Wilcox WR.
    Am J Med Genet; 1998 Jan 06; 75(1):95-100. PubMed ID: 9450865
    [Abstract] [Full Text] [Related]

  • 50. Atelosteogenesis type III: a distinct skeletal dysplasia with features overlapping atelosteogenesis and oto-palato-digital syndrome type II.
    Stern HJ, Graham JM, Lachman RS, Horton W, Bernini PM, Spiegel PK, Bodurtha J, Ives EJ, Bocian M, Rimoin DL.
    Am J Med Genet; 1990 Jun 06; 36(2):183-95. PubMed ID: 2368807
    [Abstract] [Full Text] [Related]

  • 51. Oto-palatal-digital syndromes.
    Schaefer GB, Kolodziej P, Olney AH.
    Ear Nose Throat J; 1998 Aug 06; 77(8):586-7. PubMed ID: 9745174
    [No Abstract] [Full Text] [Related]

  • 52. Spondylohumerofemoral hypoplasia (giant cell chondrodysplasia): a neonatally lethal short-limbed skeletal displasia.
    Sillence DO, Lachman RS, Jenkins T, Riccardi VM, Rimoin DL.
    Am J Med Genet; 1982 Sep 06; 13(1):7-14. PubMed ID: 6753583
    [Abstract] [Full Text] [Related]

  • 53. [Vertebral abnormalities and radius aplasia in a newborn with multiple abnormalities].
    Ostertag B.
    Z Anat Entwicklungsgesch; 1967 Aug 23; 126(2):182-204. PubMed ID: 5594117
    [No Abstract] [Full Text] [Related]

  • 54. Spondylocarpotarsal synostosis with epiphyseal dysplasia.
    Honeywell C, Langer L, Allanson J.
    Am J Med Genet; 2002 May 15; 109(4):318-22. PubMed ID: 11992487
    [Abstract] [Full Text] [Related]

  • 55. Diaphragmatic hernia and preaxial polydactyly in spondylothoracic dysplasia.
    Day R, Fryer A.
    Clin Dysmorphol; 2003 Oct 15; 12(4):277-8. PubMed ID: 14564219
    [Abstract] [Full Text] [Related]

  • 56. An unclassifiable short rib-polydactyly syndrome with acromesomelic hypomineralization and campomelia in siblings.
    Kannu P, McFarlane JH, Savarirayan R, Aftimos S.
    Am J Med Genet A; 2007 Nov 01; 143A(21):2607-11. PubMed ID: 17935248
    [Abstract] [Full Text] [Related]

  • 57. Thanatophoric dysplasia. A report of three cases.
    Sundkvist L.
    Acta Pathol Microbiol Immunol Scand A; 1983 Sep 01; 91(5):335-41. PubMed ID: 6412513
    [Abstract] [Full Text] [Related]

  • 58. A lethal neonatal dwarfing condition with short ribs, polysyndactyly, cranial synostosis, cleft palate cardiovascular and urogenital anomalies and severe ossification defect.
    Piepkorn M, Karp LE, Hickok D, Wiegenstein L, Hall JG.
    Teratology; 1977 Dec 01; 16(3):345-50. PubMed ID: 594914
    [Abstract] [Full Text] [Related]

  • 59. Trisomy 22 and facioauriculovertebral (Goldenhar) sequence.
    Kobrynski L, Chitayat D, Zahed L, McGregor D, Rochon L, Brownstein S, Vekemans M, Albert DL.
    Am J Med Genet; 1993 Apr 01; 46(1):68-71. PubMed ID: 8494034
    [Abstract] [Full Text] [Related]

  • 60. De la Chapelle dysplasia (atelosteogenesis type II): case report and review of the literature [corrected].
    Schrander-Stumpel C, Havenith M, Linden EV, Maertzdorf W, Offermans J, van der Harten J.
    Clin Dysmorphol; 1994 Oct 01; 3(4):318-27. PubMed ID: 7632220
    [Abstract] [Full Text] [Related]

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