BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

109 related articles for article (PubMed ID: 5926353)

  • 1. [On the impairment of the first 2 fissures and the first 2 brachial arches. (Apropos of 8 familial cases presenting an unusual syndrome)].
    Bourguet J; Mazeas R; Le Huérou Y
    Rev Otoneuroophtalmol; 1966; 38(4):161-75. PubMed ID: 5926353
    [No Abstract]   [Full Text] [Related]  

  • 2. [Malformation of the 1st 2 branchial clefts and arches. Apropos of 8 familial cases comprising a particular syndrome].
    Bourguet J; Mazéas R; Lehuerou Y
    Ann Otolaryngol Chir Cervicofac; 1966; 83(4):317-27. PubMed ID: 5935940
    [No Abstract]   [Full Text] [Related]  

  • 3. [Deafness and familial congenital auricular fistulas].
    Bailleul JP; Libersa C; Laude M
    Pediatrie; 1972; 27(7):739-47. PubMed ID: 4659974
    [No Abstract]   [Full Text] [Related]  

  • 4. [Chronic progressive bulbopontine paralysis with deafness. A clinical syndrome].
    van Laere J
    Verh K Acad Geneeskd Belg; 1977; 39(3):126-58. PubMed ID: 605657
    [No Abstract]   [Full Text] [Related]  

  • 5. [Familial progressive chronic bulbo-pontine paralysis with deafness. A case of Klippel-Trenaunay syndrome in siblings of the same family. Diagnostic and genetic problems].
    Van Laere J
    Rev Neurol (Paris); 1966 Aug; 115(2):289-95. PubMed ID: 5969547
    [No Abstract]   [Full Text] [Related]  

  • 6. Autosomal dominant branchiootorenal dysplasia.
    Melnick M; Bixler D; Silk K; Yune H; Nance WE
    Birth Defects Orig Artic Ser; 1975; 11(5):121-8. PubMed ID: 1218203
    [No Abstract]   [Full Text] [Related]  

  • 7. [Familial studies on the heredity OF METRIC AND MORPHOLOGICAL TRAITS OF THE EXTERNAL EAR].
    Lange G
    Z Morphol Anthropol; 1966 May; 57(2):111-67. PubMed ID: 5974078
    [No Abstract]   [Full Text] [Related]  

  • 8. Frequency of the branchio-oto-renal (BOR) syndrome in children with profound hearing loss.
    Fraser FC; Sproule JR; Halal F
    Am J Med Genet; 1980; 7(3):341-9. PubMed ID: 7468659
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Recurrent or familial facial palsy. Apropos of 6 cases and review of the literature].
    Benlyazid A; Bassereau G; Heitzmann P; Foucault N
    Ann Otolaryngol Chir Cervicofac; 1995; 112(8):374-80. PubMed ID: 8729400
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Branchio-oto-renal syndrome.
    Garg A; Wadhera R; Gulati SP; Kumar A
    J Assoc Physicians India; 2008 Nov; 56():904-5. PubMed ID: 19263692
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Alport's syndrome and associated congenital malformations of the kidney and ear].
    Bérard F; Morand R
    Ann Otolaryngol Chir Cervicofac; 1967; 84(7):555-60. PubMed ID: 6073014
    [No Abstract]   [Full Text] [Related]  

  • 12. Conductive hearing loss and malformed low-set ears, as a possible recessive syndrome.
    Mengel MC; Konigsmark BW; Berlin CI; McKusick VA
    J Med Genet; 1969 Mar; 6(1):14-21. PubMed ID: 5771216
    [No Abstract]   [Full Text] [Related]  

  • 13. [Management of post-traumatic facial paralysis. Apropos of 83 cases].
    De Bonfils-Dindart C; Darrouzet V; Mbarek C; Dumon T; Diab S; Bébéar JP
    Rev Laryngol Otol Rhinol (Bord); 1995; 116(3):171-7. PubMed ID: 7569386
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Familial occurrence of relapsing facial paralysis with paralysis of the oculomotor muscles].
    Lisch K
    Klin Monbl Augenheilkd; 1969 Sep; 155(3):400-4. PubMed ID: 5354477
    [No Abstract]   [Full Text] [Related]  

  • 15. Glomerular lesions in the branchio-oto-renal (BOR) syndrome.
    Dumas R; Uziel A; Baldet P; Segond A
    Int J Pediatr Nephrol; 1982 Jun; 3(2):67-70. PubMed ID: 7107121
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Frequent appearance of auricular changes associated with deafness].
    Kleinfeldt D; Dahl D
    HNO; 1971 Sep; 19(9):273-4. PubMed ID: 5111435
    [No Abstract]   [Full Text] [Related]  

  • 17. [Waardenburg's syndrome. (Apropos of a familial case)].
    Grimaud R; Cordier J; Saudax E; Denert M
    Rev Otoneuroophtalmol; 1966; 38(2):89-91. PubMed ID: 5931088
    [No Abstract]   [Full Text] [Related]  

  • 18. [Recurrent familial idiopathic facial paralysis].
    Rousseau JJ; Godfroi ME; Husquinet H
    Acta Neurol Belg; 1983; 83(1):23-8. PubMed ID: 6858609
    [No Abstract]   [Full Text] [Related]  

  • 19. [Malformation of the external ear and angioleiomyoma of the parapharynx--syndrome of the 1st and 2d branchial arch].
    Dvorák J; Bejcek Z
    Cesk Stomatol; 1972 Nov; 72(6):404-9. PubMed ID: 4508728
    [No Abstract]   [Full Text] [Related]  

  • 20. [The different types of sclerocornea, their hereditary modes and concomitant congenital malformations].
    Bloch N
    J Genet Hum; 1965 Sep; 14(2):133-72. PubMed ID: 4954614
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.