BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

199 related articles for article (PubMed ID: 2591071)

  • 21. A new X linked syndrome with mental retardation and craniofacial dysmorphism?
    Hyde-Forster I; McCarthy G; Berry AC
    J Med Genet; 1992 Oct; 29(10):736-8. PubMed ID: 1433236
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Dandy-Walker malformation in the Meckel syndrome.
    Summers MC; Donnenfeld AE
    Am J Med Genet; 1995 Jan; 55(1):57-61. PubMed ID: 7702098
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Deletion of the short arm of chromosome 9. A clinically recognisable entity.
    Fryns JP; Pedersen JC; Duyck H; Fabry G; Van den Berghe H
    Eur J Pediatr; 1980 Sep; 134(3):201-4. PubMed ID: 7428770
    [TBL] [Abstract][Full Text] [Related]  

  • 24. X-linked inheritance of Dandy-Walker variant.
    Wakeling EL; Jolly M; Fisk NM; Gannon C; Holder SE
    Clin Dysmorphol; 2002 Jan; 11(1):15-8. PubMed ID: 11822699
    [TBL] [Abstract][Full Text] [Related]  

  • 25. New X-linked mental retardation disorder with Dandy-Walker malformation, basal ganglia disease, and seizures.
    Pettigrew AL; Jackson LG; Ledbetter DH
    Am J Med Genet; 1991; 38(2-3):200-7. PubMed ID: 2018058
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A familial syndrome of central nervous system and ocular malformations.
    Chemke J; Czernobilsky B; Mundel G; Barishak YR
    Clin Genet; 1975 Jan; 7(1):1-7. PubMed ID: 803883
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A new lethal chondrodysplasia with spondylocostal dysostosis, multiple internal anomalies and Dandy-Walker cyst.
    Moerman P; Vandenberghe K; Fryns JP; Haspeslagh M; Lauweryns JM
    Clin Genet; 1985 Feb; 27(2):160-4. PubMed ID: 3884191
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Acrocallosal syndrome in two African brothers born to consanguineous parents.
    Christianson AL; Venter PA; Du Toit JL; Shipalana N; Gericke GS
    Am J Med Genet; 1994 Jun; 51(2):98-101. PubMed ID: 8092201
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Ultrasound diagnosis of central nervous system anomalies (bifid choroid plexus, ventriculomegaly, Dandy-Walker malformation) associated with multicystic dysplastic kidney disease in a trisomy 9 fetus: case report with literature review.
    Tonni G; Grisolia G
    J Clin Ultrasound; 2013 Sep; 41(7):441-7. PubMed ID: 23055272
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Adult-onset presentation of Dandy-Walker variant in siblings.
    Engelhard HH; Meyer JR
    Surg Neurol; 1995 Jul; 44(1):43-7. PubMed ID: 7482253
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Dandy-Walker malformation in an infant with tetrasomy 9p.
    Cazorla Calleja MR; Verdú A; Félix V
    Brain Dev; 2003 Apr; 25(3):220-3. PubMed ID: 12689705
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Dandy-Walker syndrome without hydrocephalus in an adult.
    Peterson DI; Stirling K; Pena AM
    Bull Clin Neurosci; 1983; 48():115-21. PubMed ID: 6680029
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Computed tomography of abnormally shaped pediatric cranium.
    Zimmerman RA; Bilaniuk LT
    Rev Interam Radiol; 1977 Jul; 2(3):135-41. PubMed ID: 897485
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Congenital cutis laxa with ligamentous laxity and delayed development, Dandy-Walker malformation and minor heart and osseous defects.
    Biver A; De Rijcke S; Toppet V; Ledoux-Corbusier M; Van Maldergem L
    Clin Genet; 1994 Jun; 45(6):318-22. PubMed ID: 7523003
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Syndrome of microcephaly, Dandy-Walker malformation, and Wilms tumor caused by mosaic variegated aneuploidy with premature centromere division (PCD): report of a new case and review of the literature.
    Kawame H; Sugio Y; Fuyama Y; Hayashi Y; Suzuki H; Kurosawa K; Maekawa K
    J Hum Genet; 1999; 44(4):219-24. PubMed ID: 10429359
    [TBL] [Abstract][Full Text] [Related]  

  • 36. De novo interstitial long arm deletion of chromosome 3 with facial dysmorphism, Dandy-Walker variant malformation and hydrocephalus.
    Sudha T; Dawson AJ; Prasad AN; Konkin D; de Groot GW; Prasad C
    Clin Dysmorphol; 2001 Jul; 10(3):193-6. PubMed ID: 11446413
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The Fryns syndrome: diaphragmatic defects, craniofacial dysmorphism, and distal digital hypoplasia. Further evidence for autosomal recessive inheritance.
    Meinecke P; Fryns JP
    Clin Genet; 1985 Dec; 28(6):516-20. PubMed ID: 4075561
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The acrocallosal syndrome in first cousins: widening of the spectrum of clinical features and further support for autosomal recessive inheritance.
    Schinzel A
    J Med Genet; 1988 May; 25(5):332-6. PubMed ID: 3385741
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Sibs with Ritscher-Schinzel (3C) syndrome and anal malformations.
    Orstavik KH; Bechensteen AG; Fugelseth D; Orderud W
    Am J Med Genet; 1998 Jan; 75(3):300-3. PubMed ID: 9475602
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Severe intellectual disability, West syndrome, Dandy-Walker malformation, and syndactyly in a patient with partial tetrasomy 17q25.3.
    Hackmann K; Stadler A; Schallner J; Franke K; Gerlach EM; Schrock E; Rump A; Fauth C; Tinschert S; Oexle K
    Am J Med Genet A; 2013 Dec; 161A(12):3144-9. PubMed ID: 24039006
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.