BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

139 related articles for article (PubMed ID: 8281272)

  • 1. Child with fronto-facio-nasal dysplasia, Hirschsprung's disease and hypospadias.
    Fryer AE
    Clin Dysmorphol; 1993 Apr; 2(2):120-2. PubMed ID: 8281272
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Familial holoprosencephaly.
    Dallaire L; Fraser FC; Wiglesworth FW
    Birth Defects Orig Artic Ser; 1971 Jun; 7(7):136-42. PubMed ID: 5173201
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: acro-fronto-facio-nasal dysostosis syndrome.
    Richieri-Costa A; Colletto GM; Gollop TR; Masiero D
    Am J Med Genet; 1985 Apr; 20(4):631-8. PubMed ID: 2986457
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ectodermal dysplasia, ectrodactyly, cleft lip/palate syndrome without ectrodactyly.
    Sankhyan N; Kaushal RK; Sarin S
    Dermatol Online J; 2006 May; 12(4):5. PubMed ID: 17083860
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Chromosomal studies in craniofacial abnormalities].
    Ahrens K
    HNO; 1967 Apr; 15(4):106-9. PubMed ID: 5592377
    [No Abstract]   [Full Text] [Related]  

  • 6. [Hypertelorism-hypospadias (BBB) syndrome. 2 additional family studies].
    Krause M; Meinecke P; Krins M; Grote W
    Monatsschr Kinderheilkd; 1990 Jan; 138(1):31-3. PubMed ID: 2314402
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Midline field defects and Hirschsprung disease.
    Say B; Smith DP
    Am J Med Genet; 1996 Jan; 61(3):293-4. PubMed ID: 8741878
    [No Abstract]   [Full Text] [Related]  

  • 8. A novel deletion in a Pearson syndrome infant with hypospadias and cleft lip and palate.
    Lohi O; Kuusela AL; Arola M
    J Inherit Metab Dis; 2005; 28(6):1165-6. PubMed ID: 16435219
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cleft lip and palate, characteristic facial appearance, malrotation of the intestine, and lethal congenital heart disease in two sibs: a new autosomal recessive condition?
    McPherson E; Clemens M
    Am J Med Genet; 1996 Mar; 62(1):58-60. PubMed ID: 8779326
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The value of establishing the genetic component in etiology of craniofacial anomalies.
    Stewart RE
    Birth Defects Orig Artic Ser; 1980; 16(5):27-33. PubMed ID: 7448376
    [No Abstract]   [Full Text] [Related]  

  • 11. [Fronto-nasal dysplasia (apropos of 4 cases)].
    Fontaine G; Walbaum R; Poupard B; Bonte C; Dhellemmes P; Maquet E; Ythier H; Stevenard C
    J Genet Hum; 1983 Dec; 31 Suppl 5():351-65. PubMed ID: 6674411
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Van der Woude syndrome with mental retardation: case report.
    Ugwu BT; Momoh JT
    East Afr Med J; 2001 Feb; 78(2):111-2. PubMed ID: 11682943
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fronto-facio-nasal dysostosis - a new autosomal recessive syndrome.
    Gollop TR
    Am J Med Genet; 1981; 10(4):409-12. PubMed ID: 7332033
    [No Abstract]   [Full Text] [Related]  

  • 14. Mental retardation, microbrachycephaly, hypotelorism, palpebral ptosis, thin/long face, cleft lip, and lumbosacral/pelvic anomalies.
    Richieri-Costa A; Guion-Almeida ML; Ramos AL
    Am J Med Genet; 1992 Jun; 43(3):565-8. PubMed ID: 1605250
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Marden-Walker syndrome: a case report and a critical review of the literature.
    Williams MS; Josephson KD; Wargowski DS
    Clin Dysmorphol; 1993 Jul; 2(3):211-9. PubMed ID: 7506965
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Schilbach-Rott syndrome in a third family: further delineation of an autosomal dominant trait.
    Becerra-Solano LE; Casillas-Avila MP; Díaz-Rodríguez M; Nastasi-Catanese JA; Toscano-Flores JJ; Ramírez-Dueñas ML
    Genet Couns; 2007; 18(3):317-23. PubMed ID: 18019373
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Confirmation of Kapur-Toriello syndrome in an Italian patient.
    Zelante L; Candela MA; Savoia A; Gasparini P
    Clin Dysmorphol; 1999 Apr; 8(2):151-3. PubMed ID: 10319207
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hypertelorism, proptosis, ptosis, polysyndactyly, hypospadias and normal height in 3 sibs: a new syndrome?
    Naguib KK
    Am J Med Genet; 1988 Jan; 29(1):35-41. PubMed ID: 2830788
    [No Abstract]   [Full Text] [Related]  

  • 19. The telecanthus-hypospadias syndrome.
    Stevens CA; Wilroy RS
    J Med Genet; 1988 Aug; 25(8):536-42. PubMed ID: 3050099
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Distinct craniofacial syndrome of lagophthalmia and bilateral cleft lip and palate.
    Korula S; Wilson L; Salomonson J
    Am J Med Genet; 1995 Nov; 59(2):229-33. PubMed ID: 8588591
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.