BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

124 related articles for article (PubMed ID: 12402000)

  • 1. A fetus suggesting an extension of theXK-aprosencephaly spectrum phenotype.
    Kajantie E; Ammälä P; Salonen R
    Clin Dysmorphol; 2002 Oct; 11(4):299-301. PubMed ID: 12402000
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Brief clinical reports: aprosencephaly-atelencephaly and the aprosencephaly (XK) syndrome.
    Lurie IW; Nedzved MK; Lazjuk GI; Kirillova IA; Cherstvoy ED
    Am J Med Genet; 1979; 3(3):301-9. PubMed ID: 114053
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Atelencephalic aprosencephaly.
    Harris CP; Townsend JJ; Norman MG; White VA; Viskochil DH; Pysher TJ; Klatt EC
    J Child Neurol; 1994 Oct; 9(4):412-6. PubMed ID: 7822735
    [TBL] [Abstract][Full Text] [Related]  

  • 4. XK aprosencephaly and anencephaly in sibs.
    Townes PL; Reuter K; Rosquete EE; Magee BD
    Am J Med Genet; 1988 Mar; 29(3):523-8. PubMed ID: 3287923
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mosaic r(13) in an infant with aprosencephaly.
    Goldsmith CL; Tawagi GF; Carpenter BF; Speevak MD; Hunter AG
    Am J Med Genet; 1993 Sep; 47(4):531-3. PubMed ID: 8256818
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Anomalies of the forebrain with radial limb defects: Garcia-Lurie-Steinfeld syndrome?
    McPherson E; Huff D; Dunn J; Muenke M
    Birth Defects Res A Clin Mol Teratol; 2004 Aug; 70(8):537-44. PubMed ID: 15329833
    [TBL] [Abstract][Full Text] [Related]  

  • 7. XK aprosencephaly.
    al-Gazali LI; Bakalinova D; Bakir M; Nath KN
    Clin Dysmorphol; 1998 Apr; 7(2):143-7. PubMed ID: 9571288
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The XK-aprosencephaly syndrome.
    Lurie IW; Nedzed MK; Lazjuk GI; Kirillova IA; Cherstvoy ED; Ostrovskaja TI; Shved IA
    Am J Med Genet; 1980; 7(2):231-4. PubMed ID: 7193413
    [No Abstract]   [Full Text] [Related]  

  • 9. Which brain defects accompany cyclopia?
    Lurie IW; Kirillova IA; Nedzved MK; Krapiva GA
    Genet Couns; 1992; 3(3):127-32. PubMed ID: 1388930
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnosis of a case with anencephaly-omphalocele-unilateral absent radial ray.
    Ceylaner S; Ceylaner G; Altun M; Coşkun A; Danisman N
    Genet Couns; 2009; 20(2):189-93. PubMed ID: 19650417
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Lethal femoral-facial syndrome: a case with unusual manifestations.
    Gillerot Y; Fourneau C; Willems T; Van Maldergem L
    J Med Genet; 1997 Jun; 34(6):518-9. PubMed ID: 9192278
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sporadic case of apparent aprosencephaly.
    Adkins WN; Kaveggia EG
    Am J Med Genet; 1979; 3(3):311-4. PubMed ID: 484598
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Prenatal ultrasound diagnosis of Toriello-Carey syndrome.
    Paladini D; Russo MG; Tartaglione A; Loffredo A; Martinelli P
    Prenat Diagn; 2002 Dec; 22(13):1185-7. PubMed ID: 12478630
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Aprosencephaly: review of the literature and report of a case with cerebellar hypoplasia, pigmented epithelial cyst and Rathke's cleft cyst.
    Kim TS; Cho S; Dickson DW
    Acta Neuropathol; 1990; 79(4):424-31. PubMed ID: 2339594
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Neuropathology of holoprosencephaly.
    Fallet-Bianco C
    Am J Med Genet C Semin Med Genet; 2018 Jun; 178(2):214-228. PubMed ID: 30182440
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Syndromal hypothalamic hamartoblastoma with holoprosencephaly sequence, microphthalmia, pulmonary malformations, radial hypoplasia and müllerian regression: further delineation of a new syndrome?
    Verloes A; Narcy F; Fallet-Bianco C
    Clin Dysmorphol; 1995 Jan; 4(1):33-7. PubMed ID: 7735503
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of lethal multiple pterygium syndrome in mid-pregnancy.
    Sciarrone A; Verdiglione P; Botta G; Franceschini P; Todros T
    Ultrasound Obstet Gynecol; 1998 Sep; 12(3):218-9. PubMed ID: 9793197
    [No Abstract]   [Full Text] [Related]  

  • 19. "Double trouble" or an amplification of the triploidy phenotype?
    Ludwig K; Pizzi M; Fassan M; Daolio C; Margiotti K; Consoli F; Salmaso R; Rugge M
    Fetal Pediatr Pathol; 2013 Feb; 31(1):60-5. PubMed ID: 22515548
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Radial aplasia and chromosome 22q11 deletion.
    Digilio MC; Giannotti A; Marino B; Guadagni AM; Orzalesi M; Dallapiccola B
    J Med Genet; 1997 Nov; 34(11):942-4. PubMed ID: 9391893
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.