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 *

172 related articles for article (PubMed ID: 4757648)

  • 1. [Pierre Robin syndrome with associated malformations].
    Müntener M
    Schweiz Med Wochenschr; 1973 Oct; 103(43):1504-8. PubMed ID: 4757648
    [No Abstract]   [Full Text] [Related]  

  • 2. Catel-Manzke syndrome: two new patients and a critical review of the literature.
    Manzke H; Lehmann K; Klopocki E; Caliebe A
    Eur J Med Genet; 2008; 51(5):452-65. PubMed ID: 18501694
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Eye involvement in Pierre Robin syndrome].
    Schumann M; Schumann D
    Klin Monbl Augenheilkd; 1971 Apr; 158(4):554-60. PubMed ID: 5578937
    [No Abstract]   [Full Text] [Related]  

  • 4. [Pierre Robin syndrome - type and degree of developmental anomalies in 62 neonates and infants].
    Poradowska W; Reszke S; Lenkiewicz T
    Pediatr Pol; 1981 Jun; 56(6):607-11. PubMed ID: 7290796
    [No Abstract]   [Full Text] [Related]  

  • 5. [Complete trisomy 22].
    Wollina K; Seidel J; Kirchner M; Beensen V; Kelbova C
    Monatsschr Kinderheilkd; 1993 Mar; 141(3):211-3. PubMed ID: 8474467
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Orolaryngofacial malformations with recurrent attacks of asphyxia, with or without chromosome abnormalities].
    Iancu AA; Iancu A
    Pediatria (Bucur); 1969; 18(1):23-32. PubMed ID: 5780917
    [No Abstract]   [Full Text] [Related]  

  • 7. [Cystic degeneration of kidneys in children in the light of our personal observations].
    Oknińska A; Ostojska J; Bogacka-Zatorska E
    Pediatr Pol; 1973 Jun; 48(6):703-12. PubMed ID: 4721429
    [No Abstract]   [Full Text] [Related]  

  • 8. Syndrome identification case report 99: proptosis, Robin association, clenched hands, and multiple abnormalities.
    Sanderson DM; Fraser FC
    J Clin Dysmorphol; 1983; 1(2):19-21. PubMed ID: 6580389
    [No Abstract]   [Full Text] [Related]  

  • 9. Stickler syndrome: report of four cases.
    Kulkarni ML; Sureshkumar C; George VG
    Ann Dent; 1993; 52(2):23-7. PubMed ID: 8267375
    [No Abstract]   [Full Text] [Related]  

  • 10. [Does the Pierre Robin syndrome still have its justification as an etiological entity?].
    Müntener M
    Arch Julius Klaus Stift Vererbungsforsch Sozialanthropol Rassenhyg; 1968-1969; 43-44():75-89. PubMed ID: 5761619
    [No Abstract]   [Full Text] [Related]  

  • 11. A genetic follow-up study of 64 patients with the Pierre Robin complex.
    Sheffield LJ; Reiss JA; Strohm K; Gilding M
    Am J Med Genet; 1987 Sep; 28(1):25-36. PubMed ID: 3674115
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Marshall syndrome.
    Stratton RF; Lee B; Ramirez F
    Am J Med Genet; 1991 Oct; 41(1):35-8. PubMed ID: 1951461
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Familial polymorph ventricular extrasystole associated with Pierre Robin syndrome].
    Kieny JR; Stoll C; Roul G; Hessel F; Bareiss P; Sacrez A
    Arch Mal Coeur Vaiss; 1992 Nov; 85(11):1559-62. PubMed ID: 1284460
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Anatomic anomalies of P. Robin syndrome and therapeutic management].
    Anagnostopoulos D; Kandiloros D; Ioannidou D; Foroglou P; Pergamalis G; Triantafilou D; Anagnostou T
    Bull Assoc Anat (Nancy); 1996 Sep; 80(250):5-6. PubMed ID: 9162258
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Onychoheterotopia with polyonychia associated with Pierre Robin syndrome: apropos of a new case. (Trial of classifying nail ectopia)].
    Roger H; Souteyrand P; Collin JP; Vanneuville G; Teinturier P
    Ann Dermatol Venereol; 1986; 113(3):235-42. PubMed ID: 3752862
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Congenital defect of the lens in the Pierre-Robin syndrome].
    Kuchynka P; Vrabec F; Krásný J; Krepelková J
    Cesk Oftalmol; 1985 Mar; 41(2):62-5. PubMed ID: 3995610
    [No Abstract]   [Full Text] [Related]  

  • 17. Pierre-Robin syndrome: a case report.
    Chiriac A; Dawson A; Krapp M; Axt-Fliedner R
    Arch Gynecol Obstet; 2008 Jan; 277(1):95-8. PubMed ID: 17618445
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Congenital microgastria in association with Pierre-Robin sequence.
    Laurie DE; Wakeling EL
    Clin Dysmorphol; 2008 Apr; 17(2):143-144. PubMed ID: 18388790
    [No Abstract]   [Full Text] [Related]  

  • 19. Pierre Robin sequence: a series of 117 consecutive cases.
    Holder-Espinasse M; Abadie V; Cormier-Daire V; Beyler C; Manach Y; Munnich A; Lyonnet S; Couly G; Amiel J
    J Pediatr; 2001 Oct; 139(4):588-90. PubMed ID: 11598609
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The prenatal diagnosis of Pierre-Robin sequence.
    Hsieh YY; Chang CC; Tsai HD; Yang TC; Lee CC; Tsai CH
    Prenat Diagn; 1999 Jun; 19(6):567-9. PubMed ID: 10416975
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.