These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

111 related articles for article (PubMed ID: 2240024)

  • 21. Williams-Beuren syndrome in monozygotic twins with variable expression.
    Pankau R; Gosch A; Simeoni E; Wessel A
    Am J Med Genet; 1993 Sep; 47(4):475-7. PubMed ID: 8256808
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Complex malformations of the female genital tract. New types and revision of classification.
    Acién P; Acién M; Sánchez-Ferrer M
    Hum Reprod; 2004 Oct; 19(10):2377-84. PubMed ID: 15333604
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A new syndrome within the oculo-auriculo-vertebral spectrum: microtia, atresia of the external auditory canal, vertebral anomaly, and complex cardiac defects.
    Derbent M; Örün UA; Varan B; Mercan Ş; Yilmaz Z; Sahin FI; Tokel K
    Clin Dysmorphol; 2005 Jan; 14(1):27-30. PubMed ID: 15602090
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Oculo-auriculo-vertebral spectrum with vascular ring and other unusual anomalies.
    Richardson MP; Lunt PW; Marlow N; Porter HJ; Speidel BD
    Clin Dysmorphol; 1993 Apr; 2(2):142-6. PubMed ID: 8281277
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Severe case of Al Awadi/Raas-Rothschild syndrome or new, possibly autosomal recessive facio-skeleto-genital syndrome.
    Mollica F; Mazzone D; Cimino G; Opitz JM
    Am J Med Genet; 1995 Mar; 56(2):168-72. PubMed ID: 7625440
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A patient with VACTERL association, amelia and hemifacial microsomia.
    Aftimos S; Winship I
    Clin Dysmorphol; 1999 Apr; 8(2):135-7. PubMed ID: 10319203
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Overlap between VACTERL and hemifacial microsomia illustrating a spectrum of malformations seen in axial mesodermal dysplasia complex (AMDC).
    Bergmann C; Zerres K; Peschgens T; Senderek J; Hörnchen H; Rudnik-Schöneborn S
    Am J Med Genet A; 2003 Aug; 121A(2):151-5. PubMed ID: 12910495
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Postrubella secondary pigmentary retinopathy].
    Nicu C; Damian C; Glavici M
    Oftalmologia; 1993; 37(3):256-60. PubMed ID: 8338828
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Monozygotic twin aborted fetuses discordant for holoprosencephaly/synotia.
    Machin GA; Sperber GH; Wootliffe J
    Teratology; 1985 Apr; 31(2):203-15. PubMed ID: 3992489
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Monozygotic twins discordant for spondylocostal dysostosis.
    Van Thienen MN; Van der Auwera BJ
    Am J Med Genet; 1994 Oct; 52(4):483-6. PubMed ID: 7747763
    [TBL] [Abstract][Full Text] [Related]  

  • 31. New case of axial mesodermal dysplasia sequence: epidemiologic evidence of a single entity.
    Martínez-Frías ML; Gomar JL
    Am J Med Genet; 1994 Jan; 49(1):74-6. PubMed ID: 8172254
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A familial syndrome with micrognathia, cleft palate, short neck and stature, vertebral anomalies and mental retardation.
    Mathieu M; De Broca A; Bony H; Piussan C
    Genet Couns; 1993; 4(4):299-303. PubMed ID: 8110419
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Microtia and associated anomalies: statistical analysis.
    Kaye CI; Rollnick BR; Hauck WW; Martin AO; Richtsmeier JT; Nagatoshi K
    Am J Med Genet; 1989 Dec; 34(4):574-8. PubMed ID: 2624271
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Facial asymmetry, cardio-vascular anomalies and adducted thumbs as unusual symptoms in Dubowitz syndrome?
    Vogels A; Lorenzetti ME; Gillis P; Fryns JP
    Ann Genet; 1996; 39(1):31-4. PubMed ID: 9297441
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Atrioventricular canal defect and hypoplastic left heart syndrome as discordant congenital heart defects in twins.
    Digilio MC; Marino B; Giannico S; Giannotti A; Dallapiccola B
    Teratology; 1999 Oct; 60(4):206-8. PubMed ID: 10508973
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Clinical features of 149 patients with facio-auriculo-vertebral spectrum.
    Muñoz-Pedroza LA; Arenas-Sordo ML
    Acta Otorrinolaringol Esp; 2013; 64(5):359-62. PubMed ID: 23896491
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Velo-cardio-facial syndrome: a review of 120 patients.
    Goldberg R; Motzkin B; Marion R; Scambler PJ; Shprintzen RJ
    Am J Med Genet; 1993 Feb; 45(3):313-9. PubMed ID: 8434617
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The CHARGE association in a newborn infant.
    Akisü M; Ozkinay F; Ozyürek R; Küçüktaş A; Kültürsay N
    Turk J Pediatr; 1998; 40(2):283-7. PubMed ID: 9714686
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Oculo-auriculo-vertebral spectrum malformation and contralateral absence of internal carotid artery.
    Legius E; Hellemans M; Wilms G; Tillemans B; Fryns JP
    Genet Couns; 1993; 4(4):325-8. PubMed ID: 8110422
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Total situs inversus associated with the oculo-auriculo-vertebral spectrum.
    Maat-Kievit JA; Baraitser M; Winter RM
    Clin Dysmorphol; 1994 Jan; 3(1):82-6. PubMed ID: 8205328
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.