BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

256 related articles for article (PubMed ID: 6638061)

  • 1. Conductive deafness, symphalangism, and facial abnormalities: the WL syndrome in a Japanese family.
    Higashi K; Inoue S
    Am J Med Genet; 1983 Sep; 16(1):105-9. PubMed ID: 6638061
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autosomal recessive malformation syndrome with minor manifestation in the heterozygotes: a preliminary report of a possible new syndrome.
    Paes-Alves AF; Azevêdo ES; Sousa MG; Almeida-Melo N; Oliveira-Filho OJ
    Am J Med Genet; 1991 Nov; 41(2):141-52. PubMed ID: 1785624
    [TBL] [Abstract][Full Text] [Related]  

  • 3. New syndrome: mixed hearing loss, mental deficiency, growth retardation, short clubbed digits, and EEG abnormalities in monozygous female twins.
    Pfeiffer RA
    Am J Med Genet; 1987 Jul; 27(3):639-44. PubMed ID: 3631135
    [No Abstract]   [Full Text] [Related]  

  • 4. Autosomal dominant atresia of the auditory canal and conductive deafness.
    Robinow M; Jahrsdoerfer RA
    Am J Med Genet; 1979; 4(1):89-94. PubMed ID: 495656
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Conductive hearing loss, middle ear ossicular anomalies, malformed thickened lop auricles, and micrognathia. A rare autosomal dominant congenital syndrome.
    Schweitzer VG; Kemink JL; Graham MD
    Am J Otol; 1984 Jul; 5(5):387-91. PubMed ID: 6476090
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An autosomal dominant syndrome of characteristic facial appearance, preauricular pits, fifth finger clinodactyly, and tetralogy of Fallot.
    Jones MC; Waldman JD
    Am J Med Genet; 1985 Sep; 22(1):135-41. PubMed ID: 4050848
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial microtia, meatal atresia, and conductive deafness in three siblings.
    Schmid M; Schröder M; Langenbeck U
    Am J Med Genet; 1985 Oct; 22(2):327-32. PubMed ID: 4050865
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An autosomal dominant facio-audio symphalangism syndrome with Klippel-Feil anomaly: a new variant of multiple synostoses.
    Pfeiffer RA; Rott HD; Angerstein W
    Genet Couns; 1990; 1(2):133-40. PubMed ID: 2080998
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Proximal symphalangism associated with conductive hearing loss.
    Akama H; Kiyotaki M; Motojima S
    Arthritis Care Res; 2000 Oct; 13(5):333-4. PubMed ID: 14635304
    [No Abstract]   [Full Text] [Related]  

  • 10. An autosomal dominant inherited syndrome with congenital stapes ankylosis.
    Teunissen B; Cremers WR
    Laryngoscope; 1990 Apr; 100(4):380-4. PubMed ID: 2319886
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A distinct dominant form of microtia and conductive hearing loss.
    Sánchez-Corona J; García-Cruz D; Ruenes R; Cantú JM
    Birth Defects Orig Artic Ser; 1982; 18(3B):211-6. PubMed ID: 7139104
    [No Abstract]   [Full Text] [Related]  

  • 12. Autosomal dominant inheritance of conductive deafness due to stapedial anomalies, external ear malformations and congenital facial palsy.
    Sellars S; Beighton P
    Clin Genet; 1983 May; 23(5):376-9. PubMed ID: 6851230
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndrome.
    Takahashi T; Takahashi I; Komatsu M; Sawaishi Y; Higashi K; Nishimura G; Saito H; Takada G
    Clin Genet; 2001 Dec; 60(6):447-51. PubMed ID: 11846737
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The autosomal dominant syndrome with congenital stapes ankylosis, broad thumbs and hyperopia.
    Hilhorst-Hofstee Y; Watkin PM; Hall CM; Baraitser M
    Clin Dysmorphol; 1997 Jul; 6(3):195-203. PubMed ID: 9220188
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Conductive deafness with ptosis and skeletal malformations in sibs: a probably autosomal recessive disorder.
    Jackson LG; Barr MA
    Birth Defects Orig Artic Ser; 1978; 14(6B):199-204. PubMed ID: 728561
    [No Abstract]   [Full Text] [Related]  

  • 16. Dominant symphalangism and conductive hearing loss.
    Makowski A; Latkowski B; Niebudek-Bogusz E
    Rev Laryngol Otol Rhinol (Bord); 1995; 116(5):339-40. PubMed ID: 8677370
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Autosomal dominant microtia.
    Chafai Elalaoui S; Cherkaoui Jaouad I; Rifai L; Sefiani A
    Eur J Med Genet; 2010; 53(2):100-3. PubMed ID: 20152949
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Symphalangism and its introduction into Hawaii: a pedigree.
    Gaal SA; Doyle JR; Larsen IJ
    Hawaii Med J; 1987 Aug; 46(8):305-7. PubMed ID: 3667255
    [No Abstract]   [Full Text] [Related]  

  • 19. Previously undescribed syndrome of craniofacial, hand anomalies, and sensorineural deafness.
    Sommer A; Young-Wee T; Frye T
    Am J Med Genet; 1983 May; 15(1):71-7. PubMed ID: 6859126
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ruvalcaba syndrome: autosomal dominant inheritance.
    Sugio Y; Kajii T
    Am J Med Genet; 1984 Dec; 19(4):741-53. PubMed ID: 6517098
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.