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 *

99 related articles for article (PubMed ID: 340801)

  • 1. Differential diagnosis on the basis of physical findings.
    Hanshaw JB; Dudgeon JA
    Major Probl Clin Pediatr; 1978; 17():278-300. PubMed ID: 340801
    [No Abstract]   [Full Text] [Related]  

  • 2. Syndrome of mental retardation, cleft palate, eventration of diaphragm, congenital heart defect, glaucoma, growth failure and craniosynostosis.
    Lowry RB; MacLean JR
    Birth Defects Orig Artic Ser; 1977; 13(3B):203-28. PubMed ID: 890093
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A new case of Balci's syndrome (corneal opacity, microphthalmia, microcephaly, mental retardation, and generalized muscular spasticity associated with congenital heart disease).
    Balci S; Demirçeken FG; Ocal B; Zorlu P; Teziç T
    Turk J Pediatr; 2001; 43(4):366-8. PubMed ID: 11765173
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Smith-Lemli-Opitz syndrome with cardiovascular abnormality.
    Robinson CD; Perry LW; Barlee A; Mella GW
    Pediatrics; 1971 May; 47(5):844-7. PubMed ID: 5573870
    [No Abstract]   [Full Text] [Related]  

  • 5. [The course of congenital toxoplasmosis. Critical study of 12 treated cases].
    Martin C; Bentegeat J; Bildstein G; Beauvieux YJ; Boisseau M; de Joigny C
    Ann Pediatr (Paris); 1969 Feb; 16(2):117-28. PubMed ID: 5785175
    [No Abstract]   [Full Text] [Related]  

  • 6. [Neonatal jaundice and the differential diagnosis of neonatal hepatosplenomegaly (author's transl)].
    Bachmann KD
    Geburtshilfe Frauenheilkd; 1974 Aug; 34(8):597-606. PubMed ID: 4372127
    [No Abstract]   [Full Text] [Related]  

  • 7. [Townes-Brocks syndrome. Case report and review of the literature].
    Kotzot D; Lorenz P; Bieber A; Gröbe H
    Monatsschr Kinderheilkd; 1992 Jun; 140(6):343-5. PubMed ID: 1640945
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Description of a case of rubella embryopathy].
    Gullo A; Gerbasi F
    Pediatria (Napoli); 1973 Oct; 81(3):502-20. PubMed ID: 4767798
    [No Abstract]   [Full Text] [Related]  

  • 9. A case of cardio-facio-cutaneous syndrome.
    Mucklow ES
    Am J Med Genet; 1989 Aug; 33(4):474-5. PubMed ID: 2596506
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Manifestation of congenital rubella syndrome: clinical and epidemiologic aspects].
    Lahbil D; Souldi L; Rais L; Lamari H; El Kettani A; Zaghloul K
    Bull Soc Belge Ophtalmol; 2007; (303):13-20. PubMed ID: 17894282
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [CHARGE association: 4 case reports].
    Siala Gaigi S; Masmoudi A; Souissi MH; Chabchoub A; Chelli H; Khrouf N
    Tunis Med; 1999 May; 77(5):297-302. PubMed ID: 10516817
    [No Abstract]   [Full Text] [Related]  

  • 12. Review of cases presenting with microcephaly and bilateral congenital cataract in a paediatric cataract clinic.
    Goyal R; Thompson D; Timms C; Wilson LC; Russell-Eggitt I
    Eye (Lond); 2008 Feb; 22(2):273-81. PubMed ID: 17975563
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Difficulties in the diagnosis of congenital toxoplasmosis in newborn infants].
    Norska-Borówka I; Godula-Stuglik U; Gajewska J
    Wiad Parazytol; 1985; 31(2):147-52. PubMed ID: 4082593
    [No Abstract]   [Full Text] [Related]  

  • 14. Macroglossia, omphalocele, visceromegaly, cytomegaly of the adrenal cortex and neonatal hypoglycemia.
    Cohen MM
    Birth Defects Orig Artic Ser; 1971 Jun; 7(7):226-32. PubMed ID: 4950924
    [No Abstract]   [Full Text] [Related]  

  • 15. Congenital intrauterine infection like syndrome of microcephaly, intracranial calcification and CNS disease.
    Mishra D; Gupta VK; Nandan D; Behal D
    Indian Pediatr; 2002 Sep; 39(9):866-9. PubMed ID: 12368535
    [No Abstract]   [Full Text] [Related]  

  • 16. Glaucoma in the congenital rubella syndrome.
    Boniuk M
    Int Ophthalmol Clin; 1972; 12(2):121-36. PubMed ID: 4121209
    [No Abstract]   [Full Text] [Related]  

  • 17. Microcephaly, microphthalmia, congenital cataract, optic atrophy, short stature, hypotonia, severe psychomotor retardation, and cerebral malformations: a second family with micro syndrome or a new syndrome?
    Mégarbané A; Choueiri R; Bleik J; Mezzina M; Caillaud C
    J Med Genet; 1999 Aug; 36(8):637-40. PubMed ID: 10465117
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Cardiac symptoms in 2 patients with Seckel syndrome].
    Rappen U; von Brenndorff AI
    Monatsschr Kinderheilkd; 1993 Jul; 141(7):584-6. PubMed ID: 8413337
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The early diagnosis of biliary atresia.
    Kimura S
    Prog Pediatr Surg; 1974; 6():91-112. PubMed ID: 4819433
    [No Abstract]   [Full Text] [Related]  

  • 20. [Differential diagnosis of mentally retarded children--report of 2 cases on the Smith-Lemli-Opitz syndrome].
    Kofer J
    Cesk Pediatr; 1976 Aug; 31(8):465-6. PubMed ID: 975364
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.