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 *

189 related articles for article (PubMed ID: 18813423)

  • 61. Gomez-Lopez-Hernandez syndrome: an easily missed diagnosis.
    Poretti A; Bartholdi D; Gobara S; Alber FD; Boltshauser E
    Eur J Med Genet; 2008; 51(3):197-208. PubMed ID: 18342593
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Oculoauriculovertebral spectrum in an infant of diabetic mother.
    Chen LT; Chang ML
    Acta Paediatr Taiwan; 2004; 45(6):346-9. PubMed ID: 15868852
    [TBL] [Abstract][Full Text] [Related]  

  • 63. [Congenital thrombopenic syndrome].
    Zergollern L; Mosnicka M; Zergollern S; Urbas N
    Srp Arh Celok Lek; 1972 Feb; 100(2):211-23. PubMed ID: 5040098
    [No Abstract]   [Full Text] [Related]  

  • 64. Urorectal septum malformation sequence: a report of seven cases.
    Jain D; Sharma MC; Kulkarni KK; Aggrawal S; Karak AK
    Congenit Anom (Kyoto); 2008 Dec; 48(4):174-9. PubMed ID: 18983585
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Townes-Brocks syndrome.
    König R; Schick U; Fuchs S
    Eur J Pediatr; 1990 Dec; 150(2):100-3. PubMed ID: 2279502
    [TBL] [Abstract][Full Text] [Related]  

  • 66. [PELVIS/SACRAL syndrome with livedoid haemangioma and amniotic band].
    Bourrat E; Lemarchand-Venencie F; Jacquemont ML; El Ghoneimi A; Wassef M; Leger J; Morel P
    Ann Dermatol Venereol; 2008 Dec; 135(12):855-9. PubMed ID: 19084698
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Berry syndrome in association with familial limb malformation.
    Shahdadpuri R; Prendiville T; Nölke L; McMahon CJ
    Ir Med J; 2009 Feb; 102(2):54-6. PubMed ID: 19405322
    [TBL] [Abstract][Full Text] [Related]  

  • 68. A sporadic case of Lenz microphthalmia syndrome.
    Antoniades K; Tzouvelekis G; Doudou A; Nanas C
    Ann Ophthalmol; 1993 Sep; 25(9):342-5. PubMed ID: 8297071
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Radial longitudinal deficiency: the incidence of associated medical and musculoskeletal conditions.
    Goldfarb CA; Wall L; Manske PR
    J Hand Surg Am; 2006 Sep; 31(7):1176-82. PubMed ID: 16945723
    [TBL] [Abstract][Full Text] [Related]  

  • 70. A Genotyped Case of Townes-Brocks Syndrome with Absent Pulmonary Valve Syndrome from Turkey.
    Ilhan O; Gumus E; Hakan N; Istar H; Harmandar B; Olgun H; Karakus SC; Cullu N; Kohlhase J; Sutherland JD; Barrio R
    J Pediatr Genet; 2024 Jun; 13(2):139-143. PubMed ID: 38721582
    [TBL] [Abstract][Full Text] [Related]  

  • 71. [MURCS association: a challenging diagnosis].
    Vergnes C; Cordier MP; Dubois R; Bouvier R; Cochat P
    Arch Pediatr; 2005 Jan; 12(1):49-51. PubMed ID: 15653055
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Townes-Brocks and Pendred syndrome in the same patient.
    Yano S; Watanabe Y; Yoshino M; Aida K; Kato H
    Am J Med Genet; 1998 May; 77(4):330-1. PubMed ID: 9600745
    [No Abstract]   [Full Text] [Related]  

  • 73. A case with bilateral radio-ulnar synostosis.
    Koç A; Kaymak AO; Karaer K; Ergün MA; Aksu T; Perçin EF
    Genet Couns; 2008; 19(2):193-8. PubMed ID: 18618994
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Congenital amegakaryocytic thrombocytopenia: the diagnostic importance of combining pathology with molecular genetics.
    Rose MJ; Nicol KK; Skeens MA; Gross TG; Kerlin BA
    Pediatr Blood Cancer; 2008 Jun; 50(6):1263-5. PubMed ID: 18240171
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Variable expressivity of renal involvement in a further family with Townes-Brocks syndrome.
    Eker HK; Balasar Ö
    Clin Dysmorphol; 2015 Jan; 24(1):24-5. PubMed ID: 25192472
    [No Abstract]   [Full Text] [Related]  

  • 76. Congenital pyloric atresia: the spectrum.
    Al-Salem A; Nawaz A; Matta H; Jacobsz A
    Int Surg; 2002; 87(3):147-51. PubMed ID: 12403088
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Kidney failure in Townes-Brocks syndrome: an under recognized phenomenon?
    Reardon W; Casserly LF; Birkenhäger R; Kohlhase J
    Am J Med Genet A; 2007 Nov; 143A(21):2588-91. PubMed ID: 17910067
    [TBL] [Abstract][Full Text] [Related]  

  • 78. PHACES syndrome--case report and literature review.
    Roganović J; Adams D
    Coll Antropol; 2009 Mar; 33(1):311-4. PubMed ID: 19408643
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Aplasia cutis congenita of the scalp, skull and dura associated with Adams-Oliver syndrome.
    Bilginer B; Onal MB; Bahadir S; Akalan N
    Turk Neurosurg; 2008 Apr; 18(2):191-3. PubMed ID: 18597236
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Fibular aplasia with ectrodactyly--broadening the clinical spectrum.
    Gieruszczak-Bialek D; Oldak M; Skorka A; Waligora J; Korniszewski L
    Eur J Med Genet; 2006; 49(1):83-6. PubMed ID: 16473314
    [TBL] [Abstract][Full Text] [Related]  

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