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 *

159 related articles for article (PubMed ID: 10794262)

  • 81. In-depth phenotyping of a Donnai-Barrow patient helps clarify proximal tubule dysfunction.
    Dachy A; Paquot F; Debray G; Bovy C; Christensen EI; Collard L; Jouret F
    Pediatr Nephrol; 2015 Jun; 30(6):1027-31. PubMed ID: 25822460
    [TBL] [Abstract][Full Text] [Related]  

  • 82. [Weill-Marchesani syndrome. Study of a case].
    Jouhaud F; Augustin P; Malbrel C
    Bull Soc Ophtalmol Fr; 1984 Oct; 84(10):1107-11. PubMed ID: 6544165
    [No Abstract]   [Full Text] [Related]  

  • 83. A review of Donnai-Barrow and facio-oculo-acoustico-renal (DB/FOAR) syndrome: clinical features and differential diagnosis.
    Pober BR; Longoni M; Noonan KM
    Birth Defects Res A Clin Mol Teratol; 2009 Jan; 85(1):76-81. PubMed ID: 19089858
    [TBL] [Abstract][Full Text] [Related]  

  • 84. Septo-optic dysplasia in two siblings.
    Benner JD; Preslan MW; Gratz E; Joslyn J; Schwartz M; Kelman S
    Am J Ophthalmol; 1990 Jun; 109(6):632-7. PubMed ID: 2346191
    [TBL] [Abstract][Full Text] [Related]  

  • 85. [Computed tomography appearance of agenesis of the corpus callosum. A report of 5 cases (author's transl)].
    Coursault R; Delouvrier JJ; Desbleds MT; Marsault C; Nahum H
    J Radiol; 1981 Feb; 62(2):103-6. PubMed ID: 7252897
    [No Abstract]   [Full Text] [Related]  

  • 86. Agenesis of the corpus callosum in Schinzel-Giedion syndrome associated with 47,XXY karyotype.
    Ozkinay FF; Akisü M; Kültürsay N; Oral R; Tansug N; Sapmaz G
    Clin Genet; 1996 Sep; 50(3):145-8. PubMed ID: 8946113
    [TBL] [Abstract][Full Text] [Related]  

  • 87. Chondrodysplasia punctata with retinal colobomas: radiographic findings.
    Herman TE
    J Perinatol; 1998; 18(2):152-5. PubMed ID: 9605308
    [No Abstract]   [Full Text] [Related]  

  • 88. The acrocallosal syndrome in a Turkish boy.
    Yüksel M; Caliskan M; Oğur G; Ozmen M; Dolunay G; Apak S
    J Med Genet; 1990 Jan; 27(1):48-9. PubMed ID: 2308155
    [TBL] [Abstract][Full Text] [Related]  

  • 89. Acrocallosal syndrome in a girl born to consanguineous parents.
    Salgado LJ; Ali CA; Castilla EE
    Am J Med Genet; 1989 Mar; 32(3):298-300. PubMed ID: 2729348
    [TBL] [Abstract][Full Text] [Related]  

  • 90. The normal, absent, and abnormal corpus callosum: sonographic findings.
    Babcock DS
    Radiology; 1984 May; 151(2):449-53. PubMed ID: 6709917
    [TBL] [Abstract][Full Text] [Related]  

  • 91. Provisionally unique autosomal recessive chondrodysplasia punctata syndrome.
    Toriello HV; Higgins JV; Miller T
    Am J Med Genet; 1993 Oct; 47(5):797-9. PubMed ID: 8267015
    [TBL] [Abstract][Full Text] [Related]  

  • 92. Two sisters with Toriello-Carey syndrome.
    Chinen Y; Tohma T; Izumikawa Y; Taketomi H; Iha T; Ohta T; Naritomi K
    Am J Med Genet; 1999 Nov; 87(3):262-4. PubMed ID: 10564882
    [TBL] [Abstract][Full Text] [Related]  

  • 93. Evidence for possible Mendelian inheritance of septo-optic dysplasia.
    Wales JK; Quarrell OW
    Acta Paediatr; 1996 Mar; 85(3):391-2. PubMed ID: 8696006
    [TBL] [Abstract][Full Text] [Related]  

  • 94. Aicardi's syndrome. A clinicopathological report.
    Allaire GS; Michaud J; Polomeno RC; Dubé J
    Can J Ophthalmol; 1995 Apr; 30(3):154-8. PubMed ID: 7627904
    [No Abstract]   [Full Text] [Related]  

  • 95. [Heterochromia iridis, congenital deafness and skin pigmentary abnormalities: Waardenburg syndrome].
    Jiménez Gómez N; Ballester Martínez MA; Urrutia Hernando S; Jaén Olasolo P
    Med Clin (Barc); 2014 Mar; 142(6):e11. PubMed ID: 24029453
    [No Abstract]   [Full Text] [Related]  

  • 96. Previously undescribed syndrome of craniofacial, hand anomalies, and sensorineural deafness.
    Sommer A; Young-Wee T; Frye T
    Am J Med Genet; 1983 May; 15(1):71-7. PubMed ID: 6859126
    [TBL] [Abstract][Full Text] [Related]  

  • 97. Cat's eye syndrome with cleft soft palate.
    Nakamura K
    Ann Plast Surg; 1985 Jan; 14(1):77-80. PubMed ID: 3856414
    [TBL] [Abstract][Full Text] [Related]  

  • 98. Ophthalmic and systemic findings in interstitial deletions of chromosome 14q: a case report and literature review.
    Pearce ZD; Droste PJ; Aaberg TM; Hassan AS
    Ophthalmic Genet; 2012 Sep; 33(3):161-6. PubMed ID: 22486322
    [TBL] [Abstract][Full Text] [Related]  

  • 99. Unexpected familial recurrence of iris coloboma. A delayed mutation mechanism?
    Barros-Nuñez P; Medina C; Mendoza R; Sanchez-Corona J; Garcia-Cruz D
    Clin Genet; 1995 Sep; 48(3):160-1. PubMed ID: 8556825
    [TBL] [Abstract][Full Text] [Related]  

  • 100. Agenesis of the corpus callosum and macrocephaly in siblings.
    Young ID; Trounce JQ; Levene MI; Fitzsimmons JS; Moore JR
    Clin Genet; 1985 Sep; 28(3):225-30. PubMed ID: 3905089
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.