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 *

114 related articles for article (PubMed ID: 3796538)

  • 21. [Craniofacial surgery in Göteborg].
    Johanson B; Lauritzen C; Andersson H; Ridell A; Friede H; Eriksson E; Lilja J; Svendsen P
    Lakartidningen; 1981 May; 78(22):2223-8. PubMed ID: 7266158
    [No Abstract]   [Full Text] [Related]  

  • 22. [Craniofacial dysmorphism with flexion of the fingers. Marden-Walker syndrome? (author's transl)].
    Kubryk N; Borde M
    Ann Pediatr (Paris); 1982 Mar; 29(3):208-10. PubMed ID: 6177274
    [No Abstract]   [Full Text] [Related]  

  • 23. Perspectives on craniofacial growth.
    Ohman JC; Richtsmeier JT
    Clin Plast Surg; 1994 Oct; 21(4):489-99. PubMed ID: 7813150
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Preoperative anthropometric dysmorphology in metopic synostosis.
    Kolar JC; Salter EM
    Am J Phys Anthropol; 1997 Jul; 103(3):341-51. PubMed ID: 9261497
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Dwarfism with high and narrow vertebrae. 2 new cases].
    Rochiccioli P; Malpuech G
    Ann Pediatr (Paris); 1983 Nov; 30(9):709-12. PubMed ID: 6660804
    [No Abstract]   [Full Text] [Related]  

  • 26. [An unusual morbid association: oligophrenia with craniofacial dysmorphism (including hypertelorism), absence of the nails and terminal phalanges of the 4th and 5th fingers and other malformations in a 7-year-old girl].
    Măgureanu S; Christodorescu D; Ciovirnache M; Constantinescu E
    Neurol Psihiatr Neurochir; 1973; 18(3):255-62. PubMed ID: 4747309
    [No Abstract]   [Full Text] [Related]  

  • 27. Hypospadias as a new congenital anomaly in Bowen-Conradi syndrome.
    Aynaci FM; Mocan H; Erduran E; Gedik Y
    Genet Couns; 1994; 5(4):369-71. PubMed ID: 7888139
    [No Abstract]   [Full Text] [Related]  

  • 28. Further experience in the management of craniofacial dysmorphic states.
    Nagib MG; Wisiol ES; Shilling BB; Purcell TW; Tubman DE
    Minn Med; 1985 Jul; 68(7):521-5. PubMed ID: 4021967
    [No Abstract]   [Full Text] [Related]  

  • 29. Parietal bone agenesis and associated multiple congenital anomalies.
    de Heer IM; van Nesselrooij BP; Spliet W; Vermeij-Keers C
    J Craniofac Surg; 2003 Mar; 14(2):192-6. PubMed ID: 12621289
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Craniofacial surgery].
    Lyberg T
    Tidsskr Nor Laegeforen; 1996 Jan; 116(2):230-4. PubMed ID: 8633330
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Genetic morphological fatal syndrome. Smith-Lemli-Opitz syndrome].
    Henkel KE; Pfeiffer RA; Stöss H
    Pathologe; 1993 Mar; 14(2):91-2. PubMed ID: 8469651
    [No Abstract]   [Full Text] [Related]  

  • 32. [Fryns syndrome: report of the first case in the national literature].
    Rentería-Ibarra M; Frías-Márquez SG; Michel-Aceves RJ; Navarrete-Arellano M
    Bol Med Hosp Infant Mex; 1993 Sep; 50(9):666-70. PubMed ID: 8373549
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Bilateral Foramina Parietalia Permagna - A Calvarial Defect Caused by Haploinsufficiency of the Msh Homeobox 2 Gene: A Case Report and Current Literature Review.
    Kahl N; Lüsebrink N; Schubert-Bast S; Freiman TM; Kieslich M
    Neuropediatrics; 2024 Jun; 55(3):205-208. PubMed ID: 38447947
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Four siblings with malformations due to maternal epilepsy and anticonvulsants.
    Lau K; Lee A; Ch'ien L
    J Tenn Med Assoc; 1994 May; 87(5):193-4. PubMed ID: 8041159
    [No Abstract]   [Full Text] [Related]  

  • 35. [Foramina parietalia permagna. Case report].
    Esposito M
    Radiol Med; 1967 Oct; 53(10):987-91. PubMed ID: 5192126
    [No Abstract]   [Full Text] [Related]  

  • 36. [Genetic morphological fatal syndromes. The Fryns syndrome].
    Henkel KE; Pfeiffer RA; Stöss H
    Pathologe; 1993 Mar; 14(2):92-3. PubMed ID: 8469652
    [No Abstract]   [Full Text] [Related]  

  • 37. Impact of communicative disorders on otolaryngologic care of patients with craniofacial anomalies.
    Peterson-Falzone SJ
    Otolaryngol Clin North Am; 1981 Nov; 14(4):895-915. PubMed ID: 7335363
    [No Abstract]   [Full Text] [Related]  

  • 38. A new lethal sclerosing bone dysplasia.
    Kingston HM; Freeman JS; Hall CM
    Skeletal Radiol; 1991; 20(2):117-9. PubMed ID: 2020859
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Genetic morphologic fatal syndromes. Neu-Laxova syndrome].
    Henkel KE; Pfeiffer RA; Stöss H
    Pathologe; 1993 Sep; 14(5):271-3. PubMed ID: 8415438
    [No Abstract]   [Full Text] [Related]  

  • 40. [Gigantism with encephalopathy and craniofacial dysmorphism].
    Marie J; Royer P; Lévèque B; Debauchez C; Rappaport R
    Ann Pediatr (Paris); 1965 Nov; 12(11):682-91. PubMed ID: 5851848
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.