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 *

153 related articles for article (PubMed ID: 18388781)

  • 21. Robinow syndrome: report of two cases and review of the literature.
    Al Kaissi A; Bieganski T; Baranska D; Chehida FB; Gharbi H; Ghachem MB; Hendaoui L; Safi H; Kozlowski K
    Australas Radiol; 2007 Feb; 51(1):83-6. PubMed ID: 17217496
    [TBL] [Abstract][Full Text] [Related]  

  • 22. An unclassifiable short rib-polydactyly syndrome with acromesomelic hypomineralization and campomelia in siblings.
    Kannu P; McFarlane JH; Savarirayan R; Aftimos S
    Am J Med Genet A; 2007 Nov; 143A(21):2607-11. PubMed ID: 17935248
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Fryns syndrome with vertebral defects: a novel association in a Mexican infant.
    Salinas-Torres VM; Rivera H
    Genet Couns; 2014; 25(1):29-33. PubMed ID: 24783652
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A newly recognized skeletal dysplasia with rhizomelic limbs and retinitis pigmentosa.
    Mégarbané A; Melick N; Daou L
    Am J Med Genet A; 2004 Oct; 130A(2):176-80. PubMed ID: 15372527
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Severe constipation in a patient with Myhre syndrome: a case report.
    Bassett JK; Douzgou S; Kerr B
    Clin Dysmorphol; 2016 Apr; 25(2):54-7. PubMed ID: 26636501
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Craniofacial and limb defects secondary to aberrant tissue bands.
    Poland BJ; Miller JR
    J Pediatr; 1974 Jan; 84(1):156. PubMed ID: 12119941
    [No Abstract]   [Full Text] [Related]  

  • 27. Clinical and radiological findings in Schinzel-Giedion syndrome.
    Al-Mudaffer M; Oley C; Price S; Hayes I; Stewart A; Hall CM; Reardon W
    Eur J Pediatr; 2008 Dec; 167(12):1399-407. PubMed ID: 18461363
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Unusual neuroradiological features in Schinzel-Giedion syndrome: a novel case.
    Lestner JM; Chong WK; Offiiah A; Kefas J; Vandersteen AM
    Clin Dysmorphol; 2012 Jul; 21(3):152-154. PubMed ID: 22473152
    [No Abstract]   [Full Text] [Related]  

  • 29. COIF syndrome: the diversity of clinical and radiological findings.
    Prais D; Merlob P; Horev G
    Am J Med Genet; 2002 Jan; 107(2):179-80. PubMed ID: 11807895
    [No Abstract]   [Full Text] [Related]  

  • 30. Myhre syndrome: A first familial recurrence and broadening of the phenotypic spectrum.
    Meerschaut I; Beyens A; Steyaert W; De Rycke R; Bonte K; De Backer T; Janssens S; Panzer J; Plasschaert F; De Wolf D; Callewaert B
    Am J Med Genet A; 2019 Dec; 179(12):2494-2499. PubMed ID: 31595668
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Ectodermal dysplasia, cleft lip/palate, and severe cutaneous and osseous syndactyly in a mentally retarded girl: a new multiple malformation syndrome.
    Freihofer HP; Walji S; Brunner HG
    Am J Med Genet; 1997 Jun; 70(3):211-5. PubMed ID: 9188655
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Familial multiple ventricular extrasystoles, short stature, craniofacial abnormalities and digital hypoplasia: a further case of Stoll syndrome?
    Mercer CL; Keeton B; Dennis NR
    Clin Dysmorphol; 2008 Apr; 17(2):91-93. PubMed ID: 18388777
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Two cases of Temple-Baraitser syndrome: natural history and further delineation of the clinical and radiologic phenotypes.
    Shen JJ
    Clin Dysmorphol; 2015 Apr; 24(2):55-60. PubMed ID: 25629734
    [TBL] [Abstract][Full Text] [Related]  

  • 34. De Novo Mutation of KAT6B Gene Causing Atypical Say-Barber-Biesecker-Young-Simpson Syndrome or Genitopatellar Syndrome.
    Li G; Li N; Li J; Ding Y; Yu T; Wang X; Wang J
    Fetal Pediatr Pathol; 2017 Apr; 36(2):130-138. PubMed ID: 28426343
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Myhre syndrome: a rare craniofacial disorder.
    Ishibashi N; Sasaki Y; Asakura Y
    Cranio; 2014 Oct; 32(4):300-6. PubMed ID: 25252769
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Hanhart syndrome.
    Dogan DG; Dogan M; Aslan M; Menekse E; Yakinci C
    Genet Couns; 2010; 21(4):359-62. PubMed ID: 21290964
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Myhre and LAPS syndromes: clinical and molecular review of 32 patients.
    Michot C; Le Goff C; Mahaut C; Afenjar A; Brooks AS; Campeau PM; Destree A; Di Rocco M; Donnai D; Hennekam R; Heron D; Jacquemont S; Kannu P; Lin AE; Manouvrier-Hanu S; Mansour S; Marlin S; McGowan R; Murphy H; Raas-Rothschild A; Rio M; Simon M; Stolte-Dijkstra I; Stone JR; Sznajer Y; Tolmie J; Touraine R; van den Ende J; Van der Aa N; van Essen T; Verloes A; Munnich A; Cormier-Daire V
    Eur J Hum Genet; 2014 Nov; 22(11):1272-7. PubMed ID: 24424121
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Roentgen rounds #90. Newborn with club feet and dislocatable hips, knees, and elbows. Campomelic dysplasia.
    McAlister WH; Applewhite T; Taysi K; Gilula LA
    Orthop Rev; 1987 Sep; 16(9):687-90. PubMed ID: 3453994
    [No Abstract]   [Full Text] [Related]  

  • 39. Ophthalmoacromelic syndrome: two further cases expanding the phenotype.
    Gambhir PS; Gambhir SP; Bankar SM
    Clin Dysmorphol; 2010 Apr; 19(2):91-94. PubMed ID: 20179580
    [No Abstract]   [Full Text] [Related]  

  • 40. Solitary median maxillary central incisor and congenital nasal pyriform aperture stenosis combined with asymmetric crying facies and postaxial lower limb reduction defects: a unique combination of features.
    Van Dijk FS; van Thuijl HF; Wermeskerken A; van Rijn RR; Cobben JM
    Eur J Med Genet; 2011; 54(3):284-6. PubMed ID: 21167328
    [TBL] [Abstract][Full Text] [Related]  

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