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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 4812212)

  • 61. [Cardiac malformations and genetic syndromes].
    Cardoso CR
    Arq Bras Cardiol; 1983 Sep; 41(3):167-70. PubMed ID: 6232909
    [No Abstract]   [Full Text] [Related]  

  • 62. Congenital contractural arachnodactyly.
    Bjerkreim I; Skogland LB; Trygstad O
    Acta Orthop Scand; 1976 Jun; 47(3):250-3. PubMed ID: 986113
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Congenital contractural arachnodactyly in a black African kindred.
    Wainer S; Vos ET
    Cent Afr J Med; 1991 Aug; 37(8):262-4. PubMed ID: 1807801
    [TBL] [Abstract][Full Text] [Related]  

  • 64. [Congenital glaucoma with dominant heredity associated with ocular and somatic malformations (Rieger's syndrome)].
    Deimarcelle Y
    Ann Ocul (Paris); 1968 Feb; 201(2):132-57. PubMed ID: 4970667
    [No Abstract]   [Full Text] [Related]  

  • 65. Congenital contractural arachnodactyly in a black family.
    Steg NL
    Birth Defects Orig Artic Ser; 1975; 11(6):57-62. PubMed ID: 1201351
    [No Abstract]   [Full Text] [Related]  

  • 66. Arachnodactyly represented in art.
    Pyeritz RE
    Am J Med Genet C Semin Med Genet; 2021 Jun; 187(2):163-167. PubMed ID: 34021688
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Congenital contractural arachnodactyly, keratoconus, and probable Marfan syndrome in the same pedigree.
    Bass HN; Sparkes RS; Crandall BF; Marcy SM
    J Pediatr; 1981 Apr; 98(4):591-3. PubMed ID: 7205489
    [No Abstract]   [Full Text] [Related]  

  • 68. Congenital contractural arachnodactyly (Beals-Hecht syndrome): a rare connective tissue disorder.
    Jurko A; Krsiakova J; Minarik M; Tonhajzerova I
    Wien Klin Wochenschr; 2013 May; 125(9-10):288-90. PubMed ID: 23595522
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Congenital muscular dystrophy with arachnodactyly.
    Kabra SK; Deorari AK; Paul VK; Sarkar C; Singh M
    Indian Pediatr; 1990 Mar; 27(3):298-300. PubMed ID: 2351454
    [No Abstract]   [Full Text] [Related]  

  • 70. [10 congenital trigger fingers. Apropos of a case].
    Moutet F; Lebrun C; Sartorius C
    Ann Pediatr (Paris); 1988 Apr; 35(4):275-8. PubMed ID: 3389702
    [No Abstract]   [Full Text] [Related]  

  • 71. [Association of arachnodactyly, microcephaly & thrombopenia in a dystrophic infant].
    PIELAGE JH
    Maandschr Kindergeneeskd; 1958 Feb; 26(2):59-63. PubMed ID: 13540362
    [No Abstract]   [Full Text] [Related]  

  • 72. [Marfan-related conditions].
    Minami S
    Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):538-41. PubMed ID: 9645128
    [No Abstract]   [Full Text] [Related]  

  • 73. Generalized skeletal abnormalities.
    Watt AJ; Chung KC
    Hand Clin; 2009 May; 25(2):265-76. PubMed ID: 19380065
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Characteristic facial dysmorphism, arachnodactyly and mental handicap in two unrelated girls: a distinct MCA/MR syndrome?
    de Die-Smulders C; Vles H; Fryns JP
    Genet Couns; 1993; 4(2):165-7. PubMed ID: 8357568
    [TBL] [Abstract][Full Text] [Related]  

  • 75. An infant with Marfanoid phenotype and congenital contractures associated with ocular and cardiovascular anomalies, cerebral white matter hypoplasia and spinal axonopathy.
    Tamminga P; Jennekens FG; Barth PG; Fleury P; van den Berg H; Oorthuys JW
    Eur J Pediatr; 1985 Jan; 143(3):228-31. PubMed ID: 3921377
    [TBL] [Abstract][Full Text] [Related]  

  • 76. [Congenital contractural arachnodactylia].
    Miotti A; Zanchetta G
    G Stomatol Ortognatodonzia; 1985; 4(3):81-4. PubMed ID: 3869601
    [No Abstract]   [Full Text] [Related]  

  • 77. Marfan syndrome. Onset and development of cardiovascular lesions in Marfan syndrome.
    Papaioannou AC; Matsaniotis N; Cantez T; Durst MD
    Angiology; 1970 Oct; 21(9):580-90. PubMed ID: 5457220
    [No Abstract]   [Full Text] [Related]  

  • 78. Characteristic facial dysmorphism, arachnodactyly and mental retardation: another case.
    Van Buggenhout GJ; Akkermans-Scholten AC; Hamel BC
    Genet Couns; 1995; 6(1):61-3. PubMed ID: 7794564
    [No Abstract]   [Full Text] [Related]  

  • 79. [Arachnodactyly and arthrogryposis. Report of a case in an infant with association of both diseases].
    AVENDANO A; FANTA E
    Pediatria (Santiago); 1963; 6():47-54. PubMed ID: 13965640
    [No Abstract]   [Full Text] [Related]  

  • 80. Roberts syndrome: facial dysmorphology in a mildly affected case.
    Ahmed AA; Imrie S; Duncan R; Tolmie J
    Clin Dysmorphol; 2009 Oct; 18(4):236-7. PubMed ID: 19707122
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.