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 *

126 related articles for article (PubMed ID: 19720548)

  • 21. [Genetic diagnosis and prenatal diagnosis of Angelman syndrome].
    Wang HL; Liang DS; Xia Y; Xia C; Wu LQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Oct; 26(5):511-3. PubMed ID: 19806569
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Autism spectrum disorders: developmental disconnection syndromes.
    Geschwind DH; Levitt P
    Curr Opin Neurobiol; 2007 Feb; 17(1):103-11. PubMed ID: 17275283
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Reversible restricted diffusion of entire corpus callosum.
    Kano O; Arasaki K; Ikeda K; Iwasaki Y; Terada H; Tsunoo M
    J Neurol Sci; 2007 Mar; 254(1-2):105; author reply 106. PubMed ID: 17258233
    [No Abstract]   [Full Text] [Related]  

  • 24. Split-cord malformation in a girl with Angelman syndrome: a mere coincidence?
    Mastroyianni SD; Kontopoulos E
    Am J Med Genet; 2002 Jul; 111(1):57-60. PubMed ID: 12124736
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Further patient with Angelman syndrome due to paternal disomy of chromosome 15 and a milder phenotype.
    Gillessen-Kaesbach G; Albrecht B; Passarge E; Horsthemke B
    Am J Med Genet; 1995 Apr; 56(3):328-9. PubMed ID: 7778602
    [No Abstract]   [Full Text] [Related]  

  • 26. Angelman syndrome and hypothyroidism - coincidence or unique correlation?
    Paprocka J; Jamroz E; Kalina M; Kalina-Faska B; Malecka-Tendera E; Marszal E
    Neuro Endocrinol Lett; 2007 Oct; 28(5):545-6. PubMed ID: 17984955
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Angelman syndrome caused by loss of a marker chromosome: cytogenetic and fluorescence in situ hybridization analysis.
    Arrieta I; Criado B; Nuñez T; Telez M; Echarri A; Martinez B; Castedo S
    Psychiatr Genet; 1997; 7(4):153-8. PubMed ID: 9460799
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Do we consider Andermann syndrome in infants with agenesis of corpus callosum.
    Deda G; Caksen H; Içağasioğlu D
    Genet Couns; 2003; 14(2):249-52. PubMed ID: 12872822
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Unilateral cleft lip in a boy with Angelman syndrome.
    Rösby O; Strömme P; Sandsmark M; Ramstad K; Ormerod E; Birger van der Hagen C; Kubota T; Ledbetter DH; Orstavik KH
    J Craniofac Genet Dev Biol; 1996; 16(2):122-5. PubMed ID: 8773903
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Angelman syndrome due to a novel splicing mutation of the UBE3A gene.
    Sartori S; Anesi L; Polli R; Toldo I; Casarin A; Drigo P; Murgia A
    J Child Neurol; 2008 Aug; 23(8):912-5. PubMed ID: 18487518
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Adult-onset vanishing white matter leukoencephalopathy presenting as psychosis.
    Denier C; Orgibet A; Roffi F; Jouvent E; Buhl C; Niel F; Boespflug-Tanguy O; Said G; Ducreux D
    Neurology; 2007 May; 68(18):1538-9. PubMed ID: 17470759
    [No Abstract]   [Full Text] [Related]  

  • 32. Prognostic value of neonatal brain imaging for very low birthweight preterm infants.
    Mirmiran M
    Dev Med Child Neurol; 2013 May; 55(5):398-9. PubMed ID: 23441903
    [No Abstract]   [Full Text] [Related]  

  • 33. Angelman syndrome in adulthood.
    Laan LA; den Boer AT; Hennekam RC; Renier WO; Brouwer OF
    Am J Med Genet; 1996 Dec; 66(3):356-60. PubMed ID: 9072912
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Deletion involving D15S113 in a mother and son without Angelman syndrome: refinement of the Angelman syndrome critical deletion region.
    Michaelis RC; Skinner SA; Lethco BA; Simensen RJ; Donlon TA; Tarleton J; Phelan MC
    Am J Med Genet; 1995 Jan; 55(1):120-6. PubMed ID: 7702085
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Robertsonian (15q;15q) translocation in a child with Angelman syndrome: evidence of uniparental disomy.
    Tonk V; Schultz RA; Christian SL; Kubota T; Ledbetter DH; Wilson GN
    Am J Med Genet; 1996 Dec; 66(4):426-8. PubMed ID: 8989460
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Anaesthesia for Angelman syndrome.
    Ramanathan KR; Muthuswamy D; Jenkins BJ
    Anaesthesia; 2008 Jun; 63(6):659-61. PubMed ID: 18477280
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A case of Høyeraal-Hreidarsson syndrome: delayed myelination and hypoplasia of corpus callosum are other important signs.
    Akaboshi S; Yoshimura M; Hara T; Kageyama H; Nishikwa K; Kawakami T; Ieshima A; Takeshita K
    Neuropediatrics; 2000 Jun; 31(3):141-4. PubMed ID: 10963101
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Analysis of the characteristics of epilepsy in 37 patients with the molecular diagnosis of Angelman syndrome.
    Galván-Manso M; Campistol J; Conill J; Sanmartí FX
    Epileptic Disord; 2005 Mar; 7(1):19-25. PubMed ID: 15741136
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Characterisation of interstitial duplications and triplications of chromosome 15q11-q13.
    Roberts SE; Dennis NR; Browne CE; Willatt L; Woods G; Cross I; Jacobs PA; Thomas S
    Hum Genet; 2002 Mar; 110(3):227-34. PubMed ID: 11935334
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [A case of Angelman syndrome combined with oculocutaneous albinism].
    Li HY; Zheng H
    Zhonghua Er Ke Za Zhi; 2005 Aug; 43(8):635-6. PubMed ID: 16191288
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.