BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

136 related articles for article (PubMed ID: 7894742)

  • 1. Fetus with features of Crane-Heise syndrome and aminopterin syndrome sine aminopterin (ASSAS).
    Barnicoat AJ; Seller MJ; Bennett CP
    Clin Dysmorphol; 1994 Oct; 3(4):353-7. PubMed ID: 7894742
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Aminopterin Syndrome Sine Aminopterin (ASSA) syndrome in two siblings: further delineation of the syndrome and review of the literature.
    Krajewska-Walasek M
    Genet Couns; 1994; 5(4):345-55. PubMed ID: 7888136
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Further case of aminopterin syndrome sine aminopterin in a Spanish child.
    Garcia-Minaur S; Botella MP
    Am J Med Genet; 2000 Dec; 95(4):320-4. PubMed ID: 11186884
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Crane-Heise syndrome: a second familial case report with elaboration of phenotype.
    Zand DJ; Carpentieri D; Huff D; Medne L; Napierala D; Lee B; Zackai E
    Am J Med Genet A; 2003 Apr; 118A(3):223-8. PubMed ID: 12673651
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Osteocraniostenosis.
    Verloes A; Narcy F; Grattagliano B; Delezoide AL; Guibaud P; Schaaps JP; Le Merrer M; Maroteaux P
    J Med Genet; 1994 Oct; 31(10):772-8. PubMed ID: 7837254
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An aminopterin-like syndrome without aminopterin (ASSAS).
    Fraser FC; Anderson RA; Mulvihill JI; Preus M
    Clin Genet; 1987 Jul; 32(1):28-34. PubMed ID: 3621652
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Crane-Heise syndrome: two further case reports.
    Petit F; Devisme L; Toutain A; Houfflin-Debarge V; Dieux-Coeslier A; Manouvrier-Hanu S; Andrieux J; Holder-Espinasse M
    Eur J Med Genet; 2011; 54(2):169-72. PubMed ID: 21094705
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Acalvaria, holoprosencephaly, and facial dysmorphism syndrome.
    Sperber GH; Honoré LH; Johnson ES
    J Craniofac Genet Dev Biol Suppl; 1986; 2():319-29. PubMed ID: 3491120
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Femoral facial syndrome with bilateral agenesis of femora and preaxial polydactyly of the feet in a Chinese stillborn.
    Poon WL; Yuen MK; Ng SK; Leung YM
    Clin Imaging; 2006; 30(5):357-60. PubMed ID: 16919561
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pseudoaminopterin syndrome.
    Verloes A; Bricteux G; Koulischer L
    Am J Med Genet; 1993 Jun; 46(4):394-7. PubMed ID: 8357010
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Fryns syndrome: an autosomal recessive disorder associated with craniofacial anomalies, diaphragmatic hernia, and distal digital hypoplasia.
    Cunniff C; Jones KL; Saal HM; Stern HJ
    Pediatrics; 1990 Apr; 85(4):499-504. PubMed ID: 2314962
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Femoral hypoplasia-unusual facies syndrome].
    Aledo AG; Gracia R; Carmona MJ; Temboury MC; Laorden L; Peralta A
    An Esp Pediatr; 1984 Dec; 21(9):861-3. PubMed ID: 6529047
    [No Abstract]   [Full Text] [Related]  

  • 15. [Experimental teratological studies on facial anomalies induced in mice by bis (dichloroacetyl) diamine. I. Establishment of an animal model of the median cleft face syndrome by the administration of bis (dichloroacetyl) diamine to mice].
    Igawa HH
    Hokkaido Igaku Zasshi; 1986 Nov; 61(6):837-50. PubMed ID: 3557271
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pseudoaminopterin syndrome: clinical report with new characteristics.
    Sobreira N; Cernach M; Batista D; Brunoni D; Perez A
    Am J Med Genet A; 2009 Dec; 149A(12):2843-8. PubMed ID: 19938091
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new short rib syndrome: report of two cases.
    Beemer FA; Langer LO; Klep-de Pater JM; Hemmes AM; Bylsma JB; Pauli RM; Myers TL; Haws CC
    Am J Med Genet; 1983 Jan; 14(1):115-23. PubMed ID: 6829599
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Teratogenic effects of retinoic acid in pigtail monkeys (Macaca nemestrina). II. Craniofacial features.
    Newell-Morris L; Sirianni JE; Shepard TH; Fantel AG; Moffett BC
    Teratology; 1980 Aug; 22(1):87-101. PubMed ID: 7444803
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Michels syndrome in a Brazilian girl born to consanguineous parents.
    Guion-Almeida ML; Rodini ES
    Am J Med Genet; 1995 Jul; 57(3):377-9. PubMed ID: 7677137
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.