BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 9571282)

  • 1. Syndactyly, micrognathia and skeletal anomalies: a new syndrome?
    McGaughran J; Moore L; Russell S; Donnai D
    Clin Dysmorphol; 1998 Apr; 7(2):119-22. PubMed ID: 9571282
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ectodermal dysplasia, cleft lip/palate, and severe cutaneous and osseous syndactyly in a mentally retarded girl: a new multiple malformation syndrome.
    Freihofer HP; Walji S; Brunner HG
    Am J Med Genet; 1997 Jun; 70(3):211-5. PubMed ID: 9188655
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Trigonomicrocephaly, severe micrognathia, large ears, atrioventricular septal defect, symmetrical cutaneous syndactyly of hands and feet, and multiple café-au-lait spots: new acrocraniofacial dysostosis syndrome?
    Al-Sannaa N; Forrest CR; Teebi AS
    Am J Med Genet; 2001 Jul; 101(3):279-82. PubMed ID: 11424146
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Recurrent Fraser syndrome.
    Kiran G; Namita G; Dheeraj S
    Prenat Diagn; 2007 Feb; 27(2):184-5. PubMed ID: 17266165
    [No Abstract]   [Full Text] [Related]  

  • 5. [Case histories of congenital anomalies].
    Chojnacka A; Hubert E
    Czas Stomatol; 1984 Dec; 37(12):1009-14. PubMed ID: 6100438
    [No Abstract]   [Full Text] [Related]  

  • 6. Complex toe syndactyly with characteristic facial phenotype: a new syndrome?
    Sobreira NL; Cernach MC; Brunoni D; Perez AB
    Am J Med Genet A; 2008 Jul; 146A(13):1725-8. PubMed ID: 18512233
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hydrolethalus syndrome: report of an apparent mild case, literature review, and differential diagnosis.
    Aughton DJ; Cassidy SB
    Am J Med Genet; 1987 Aug; 27(4):935-42. PubMed ID: 3321994
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Fibrochondrogenesis in a 17-week fetus: a case expanding the phenotype.
    Hunt NC; Vujanić GM
    Am J Med Genet; 1998 Jan; 75(3):326-9. PubMed ID: 9475607
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis of a case of ectrodactyly in 2D and 3D ultrasound.
    Kang A; Visca E; Bruder E; Holzgreve W; Struben H; Tercanli S
    Ultraschall Med; 2009 Apr; 30(2):121-3. PubMed ID: 19421951
    [No Abstract]   [Full Text] [Related]  

  • 10. Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies: delineation of a new entity and review of lethal forms of multiple pterygium syndrome.
    Chen H; Immken L; Lachman R; Yang S; Rimoin DL; Rightmire D; Eteson D; Stewart F; Beemer FA; Opitz JM
    Am J Med Genet; 1984 Apr; 17(4):809-26. PubMed ID: 6720746
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Craniofacial anomalies: from development to molecular pathogenesis.
    Rice DP
    Curr Mol Med; 2005 Nov; 5(7):699-722. PubMed ID: 16305494
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Central nervous system malformations, dense bones and facial dysmorphism: a new autosomal recessive syndrome.
    al-Gazali LI; Bakalinova D; Bakir M
    Clin Dysmorphol; 1998 Apr; 7(2):123-6. PubMed ID: 9571283
    [TBL] [Abstract][Full Text] [Related]  

  • 13. First-trimester diagnosis of Bartsocas-Papas syndrome (BPS) by transvaginal ultrasound: case report and review of the literature.
    Dolan SM; Shanske AL; Marion RW; Gross SJ
    Prenat Diagn; 2003 Feb; 23(2):138-42. PubMed ID: 12575021
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Median cleft face syndrome.
    Edwards WC; Askew W; Weisskopf B
    Am J Ophthalmol; 1971 Jul; 72(1):202-5. PubMed ID: 5571207
    [No Abstract]   [Full Text] [Related]  

  • 15. Autopsy on a case of Roberts syndrome reported in 1672: the earliest description?
    Bates AW
    Am J Med Genet A; 2003 Feb; 117A(1):92-6. PubMed ID: 12548750
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cleft palate in Kabuki syndrome: a report of six cases.
    Iida T; Park S; Kato K; Kitano I
    Cleft Palate Craniofac J; 2006 Nov; 43(6):756-61. PubMed ID: 17105332
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 109(2):139-48. PubMed ID: 11977163
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Brief clinical report: lethal multiple pterygium syndrome in an 18-week fetus with hydrops.
    Isaacson G; Gargus JJ; Mahoney MJ
    Am J Med Genet; 1984 Apr; 17(4):835-9. PubMed ID: 6720748
    [TBL] [Abstract][Full Text] [Related]  

  • 19. New syndrome in three affected siblings.
    Crane JP; Heise RL
    Pediatrics; 1981 Aug; 68(2):235-7. PubMed ID: 7267231
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Severe end of Opitz trigonocephaly C syndrome.
    Lindor NM; Ramin KD; Kleinberg F; Bite U
    Am J Med Genet; 2000 Jun; 92(5):363-5. PubMed ID: 10861669
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.