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 *

116 related articles for article (PubMed ID: 7134511)

  • 1. [Case of otocraniofacial and vertebral malformation syndrome. The postnatal evolution of congenital vertebral blocks].
    Leone G
    Radiol Med; 1982; 68(7-8):592-4. PubMed ID: 7134511
    [No Abstract]   [Full Text] [Related]  

  • 2. The radiology of Coffin-Lowry syndrome.
    Padley S; Hodgson SV; Sherwood T
    Br J Radiol; 1990 Jan; 63(745):72-5. PubMed ID: 2306591
    [No Abstract]   [Full Text] [Related]  

  • 3. [Teleradiographic analysis of the face in facial asymmetry].
    Jammet P; Souyris F; Rey PA; Atlan G
    Rev Stomatol Chir Maxillofac; 1991; 92(3):188-92. PubMed ID: 1891694
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hemifacial microsomia in pediatric patients: asymmetric abnormal development of the first and second branchial arches.
    Sze RW; Paladin AM; Lee S; Cunningham ML
    AJR Am J Roentgenol; 2002 Jun; 178(6):1523-30. PubMed ID: 12034632
    [No Abstract]   [Full Text] [Related]  

  • 5. [Facial malformations and asymmetries due to first and second branchial arch syndromes].
    Van den Eynde H; Joosen E; Van Reck J; Mayer R
    Acta Stomatol Belg; 1989 Jun; 86(1):49-65. PubMed ID: 2577742
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Thymalin correction of the immunologic deficiency state in children with congenital 1st and 2d branchial arch syndrome].
    Kotov GA; Iarchuk NI; Khavinson VKh; Morozov VG; Kozhemiakin AL
    Pediatriia; 1983 May; (5):54-5. PubMed ID: 6688298
    [No Abstract]   [Full Text] [Related]  

  • 7. Multiple posterior vertebral fusion abnormalities: a case report and review of the literature.
    Chen JJ; Branstetter BF; Welch WC
    AJR Am J Roentgenol; 2006 May; 186(5):1256-9. PubMed ID: 16632715
    [No Abstract]   [Full Text] [Related]  

  • 8. [Maxillofacial reflection of choanal atresia. Apropos 11 cases].
    Hofmann B; Beauvillain de Montreuil C; Delaire J
    Rev Stomatol Chir Maxillofac; 1985; 86(5):327-33. PubMed ID: 3868005
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A rare congenital malformation: caudal regression syndrome.
    Mandour C; El Mostarchid B
    Pan Afr Med J; 2013; 14():30. PubMed ID: 23504067
    [No Abstract]   [Full Text] [Related]  

  • 10. Postnatal Diagnosis of a Baby With Multiple Rare Congenital Anomalies Including Syngnathia, Brain Dysmorphism, and Skin Pigmentation.
    Mahgoub L; Joynt C; Bhargava R; Davies D; El-Hakim H; Dobrovolsky W
    Cleft Palate Craniofac J; 2015 Nov; 52(6):e201-4. PubMed ID: 25325328
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Gnathodiaphyseal dysplasia.
    Ahluwalia J; Ly JQ; Norman E; Costello RF; Beall DP
    Clin Imaging; 2007; 31(1):67-9. PubMed ID: 17189853
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Immunological disorders and their correction with thymalin in the surgical treatment of patients with 1st and 2nd branchial arch syndromes].
    Kotov GA; Iarchuk NI; Khavinson VKh; Morozov VG
    Stomatologiia (Mosk); 1984; 63(3):43-4. PubMed ID: 6589825
    [No Abstract]   [Full Text] [Related]  

  • 13. Frontometaphyseal dysplasia.
    Holt JF; Thompson GR; Arenberg IK
    Radiol Clin North Am; 1972 Aug; 10(2):225-43. PubMed ID: 5044403
    [No Abstract]   [Full Text] [Related]  

  • 14. [Spondylocostal dysostosis and polydactylia].
    Zeller C; Babin E; Dietemann JL; Wackenheim A
    J Radiol; 1982 May; 63(5):355-7. PubMed ID: 7131402
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Apropos of a rare craniofacial abnormality of the 1st branchial arch].
    Hsissen MA; Kadiri F; Detsouli M; Touhami M; Chekkoury IA; Benchakroun Y
    Rev Laryngol Otol Rhinol (Bord); 1996; 117(2):141-4. PubMed ID: 8959936
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Unusual case of dysmorphous vertebral column (clinical and radiological aspects)].
    Collo G; Valdameri C; Callura G
    Chir Organi Mov; 1971; 60(3):297-303. PubMed ID: 5005236
    [No Abstract]   [Full Text] [Related]  

  • 17. Facial dysmorphism associated with distinctive spine abnormalities in a girl and her mother: novel syndromic association.
    Al Kaissi A; Roetzer KM; Heitzer E; Ben Chehida F; Ben Ghachem M; Klaushofer K; Grill F
    Clin Dysmorphol; 2011 Oct; 20(4):182-186. PubMed ID: 21814137
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Jarcho-Levin syndrome: a new case report with unusual unexplained aortic root dilatation.
    Galguera MA; García FL; Bauzá Rossi J; Vázquez de Corral L
    Bol Asoc Med P R; 1997; 89(7-9):134-6. PubMed ID: 9419932
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dysspondylochondromatosis.
    Freisinger P; Finidori G; Maroteaux P
    Am J Med Genet; 1993 Feb; 45(4):460-4. PubMed ID: 8465851
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [The oto-cardio-vertebral syndrome (author's transl)].
    Müller WD; Beitzke A; Kellerer K
    Klin Padiatr; 1974 May; 186(3):252-6. PubMed ID: 4472471
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.