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 *

78 related articles for article (PubMed ID: 5213336)

  • 21. [Children of phenylketonuric mothers].
    Hooft C; Carton D; Broekaert E; Devos E; de Schrijver F
    Acta Paediatr Belg; 1970; 24(1):5-19. PubMed ID: 5518455
    [No Abstract]   [Full Text] [Related]  

  • 22. A familial syndrome of mental retardation in association with multiple congenital anomalies resembling the syndrome of Smith-Lemli-Opitz.
    Kenis H; Hustinx TW
    Maandschr Kindergeneeskd; 1967 May; 35(2):37-48. PubMed ID: 6047019
    [No Abstract]   [Full Text] [Related]  

  • 23. [The oro-digito-facial syndrome. Apropos of a case].
    Maillard E; Bailleul JP; Vandenbussche F; Donazzan M; Lefebvre R; Fontaine G
    Pediatrie; 1969; 24(5):577-83. PubMed ID: 5398150
    [No Abstract]   [Full Text] [Related]  

  • 24. [Orofaciodigital (OFD) syndrome].
    Jibiinkoka; 1967 Dec; 39(12):1326. PubMed ID: 5628563
    [No Abstract]   [Full Text] [Related]  

  • 25. [A case of orofacialdigital syndrome in a chromosomally normal male].
    Theodorou S; Maounis P; Giannoulopoulos A
    Stomatologia (Athenai); 1971; 28(6):435-43. PubMed ID: 5290176
    [No Abstract]   [Full Text] [Related]  

  • 26. Coffin-Lowry syndrome in an Afro-American family.
    Kousseff BG
    Am J Med Genet; 1982 Mar; 11(3):373-5. PubMed ID: 7081302
    [No Abstract]   [Full Text] [Related]  

  • 27. [Agenesis of the corpus callosum in 2 brothers].
    Dogan K; Dogan S; Lovrencić M
    Lijec Vjesn; 1967; 89(5):377-85. PubMed ID: 6063234
    [No Abstract]   [Full Text] [Related]  

  • 28. [Minor abnormalities in children with severe mental retardation].
    Péter L; István L; Endre C
    Orv Hetil; 1978 Dec; 119(49):3010-2. PubMed ID: 714448
    [No Abstract]   [Full Text] [Related]  

  • 29. [Mental retardation in childhood. The prevalence of informative morphogenetic variants].
    Csábi G; Aradi P; Hollódy K; Tényi T
    Neuropsychopharmacol Hung; 2007 Dec; 9(4):197-200. PubMed ID: 18510264
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Autosomal cytogenetics.
    ZELLWEGER H; MIKAMO K
    Helv Paediatr Acta; 1961 Dec; 16():670-90. PubMed ID: 14010092
    [No Abstract]   [Full Text] [Related]  

  • 31. [Oro-facio-digital syndrome. 3 personal cases].
    Walbaum R; Maillard E; Donazzan M; Carbain B; Fontaine G
    Lille Med; 1970; 15(6):917-30. PubMed ID: 5454728
    [No Abstract]   [Full Text] [Related]  

  • 32. Picture of the month. Oral-facial-digital syndrome.
    Gellis SS; Feingold M; Gorlin R
    Am J Dis Child; 1970 Sep; 120(3):241-2. PubMed ID: 5458559
    [No Abstract]   [Full Text] [Related]  

  • 33. [Congenital anomalies in a family with incest].
    Seemanová E
    Cesk Pediatr; 1970 Sep; 25(9):432-3. PubMed ID: 5455606
    [No Abstract]   [Full Text] [Related]  

  • 34. Use of array CGH in the evaluation of dysmorphology, malformations, developmental delay, and idiopathic mental retardation.
    Stankiewicz P; Beaudet AL
    Curr Opin Genet Dev; 2007 Jun; 17(3):182-92. PubMed ID: 17467974
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A diagnostic survey of patients referred for chromosome analysis.
    Kosztolányi G
    Acta Paediatr Acad Sci Hung; 1982; 23(1):35-40. PubMed ID: 7090808
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Clinical application of microarray-based molecular cytogenetics: an emerging new era of genomic medicine.
    Li MM; Andersson HC
    J Pediatr; 2009 Sep; 155(3):311-7. PubMed ID: 19732576
    [No Abstract]   [Full Text] [Related]  

  • 37. The acrocallosal syndrome.
    Nelson MM; Thomson AJ
    Am J Med Genet; 1982 Jun; 12(2):195-9. PubMed ID: 7102724
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [OFD syndrome in a male. Clinical-genetic analysis of 33 families].
    Segni G; Serra A; Mastrangelo R; Polidori G; Massasso J
    Acta Genet Med Gemellol (Roma); 1970 Oct; 19(4):546-66. PubMed ID: 5512530
    [No Abstract]   [Full Text] [Related]  

  • 39. Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes.
    Riegel M; Baumer A; Jamar M; Delbecque K; Herens C; Verloes A; Schinzel A
    Hum Genet; 2001 Sep; 109(3):286-94. PubMed ID: 11702209
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Autosomal recessive syndrome of growth and mental retardation, seizures, retinal abnormalities, and osteodysplasia with similarity to the Gurrieri syndrome.
    Orrico A; Hayek G; Burroni L
    Am J Med Genet; 1999 Jan; 82(1):84-7. PubMed ID: 9916849
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.