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 *

67 related articles for article (PubMed ID: 7447745)

  • 21. Fryns syndrome survivors and neurologic outcome.
    Van Hove JL; Spiridigliozzi GA; Heinz R; McConkie-Rosell A; Iafolla AK; Kahler SG
    Am J Med Genet; 1995 Nov; 59(3):334-40. PubMed ID: 8599357
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Cerebellar hypoplasia, facial dysmorphism and internal abnormalities: a new recessive syndrome?
    Seller MJ; Pal K; Moscoso G; Nicolaides K; Hyett JA
    Clin Dysmorphol; 1998 Jan; 7(1):41-4. PubMed ID: 9546829
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Low cholesterol and pathological manifestations: Smith-Lemli-Opitz syndrome].
    Franceschini P; Franceschini D
    Minerva Pediatr; 1994 Dec; 46(12):579-80. PubMed ID: 7731422
    [No Abstract]   [Full Text] [Related]  

  • 24. Acrocallosal syndrome in two African brothers born to consanguineous parents.
    Christianson AL; Venter PA; Du Toit JL; Shipalana N; Gericke GS
    Am J Med Genet; 1994 Jun; 51(2):98-101. PubMed ID: 8092201
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Ritscher-Schinzel cranio-cerebello-cardiac (3C) syndrome: report of four new cases and review.
    Leonardi ML; Pai GS; Wilkes B; Lebel RR
    Am J Med Genet; 2001 Aug; 102(3):237-42. PubMed ID: 11484200
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Six patients with oral-facial-digital syndrome IV: the case for heterogeneity.
    Toriello HV; Carey JC; Suslak E; Desposito FR; Leonard B; Lipson M; Friedman BD; Hoyme HE
    Am J Med Genet; 1997 Mar; 69(3):250-60. PubMed ID: 9096753
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Multiple congenital anomalies associated with an oto-palato-digital syndrome type II.
    Blanchet P; Lefort G; Eglin MC; Rieu D; Sarda P
    Genet Couns; 1993; 4(4):289-94. PubMed ID: 8110417
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Antley-Bixler syndrome: case report and review of the literature.
    Poddevin F; Delobel B; Courreges P; Bayart M
    Genet Couns; 1995; 6(3):241-6. PubMed ID: 8588853
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Acro-cardio-facial syndrome associated with neuroepithelial cyst: a case report.
    Sivasli O; Ozer EA; Ozer A; Aydinlioglu H; Helvaci M
    Genet Couns; 2007; 18(2):247-50. PubMed ID: 17710878
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Fetal alcohol syndrome: craniofacial and central nervous system manifestations.
    Johnson VP; Swayze VW II; Sato Y; Andreasen NC
    Am J Med Genet; 1996 Feb; 61(4):329-39. PubMed ID: 8834044
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Cloverleaf skull and other malformations of the skull. Pathology and clinical aspect].
    Gathmann HA
    Acta Med Austriaca; 1977; 4(4-9):152-6. PubMed ID: 610339
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Toriello-Carey syndrome: report of a new case.
    Camera G; Righi E; Romagnoli G
    Clin Dysmorphol; 1993 Jul; 2(3):260-3. PubMed ID: 7506967
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Further delineation of the Baller-Gerold syndrome.
    Lin AE; McPherson E; Nwokoro NA; Clemens M; Losken HW; Mulvihill JJ
    Am J Med Genet; 1993 Feb; 45(4):519-24. PubMed ID: 8465861
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Schinzel-Giedion syndrome: autopsy report and additional clinical manifestations.
    Rodríguez JI; Jiménez-Heffernan JA; Leal J
    Am J Med Genet; 1994 Dec; 53(4):374-7. PubMed ID: 7864048
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Joubert syndrome with congenital hepatic fibrosis: an entity in the spectrum of oculo-encephalo-hepato-renal disorders.
    Lewis SM; Roberts EA; Marcon MA; Harvey E; Phillips MJ; Chuang SA; Buncic JR; Clarke JT
    Am J Med Genet; 1994 Oct; 52(4):419-26. PubMed ID: 7538263
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Two siblings with midline field defects and Hirschsprung disease: variable expression of Toriello-Carey or new syndrome?
    Jespers A; Buntinx I; Melis K; Vaerenberg M; Janssens G
    Am J Med Genet; 1993 Aug; 47(2):299-302. PubMed ID: 8213924
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The Walker-Warburg syndrome with cleft lip and palate.
    Pratap A; Agrawal A; Tiwari A; Lakshmi R; Rajbanshi S
    Singapore Med J; 2007 Feb; 48(2):e66-7. PubMed ID: 17304384
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Case report: two patients with oculocerebrocutaneous syndrome and terminal digital amputations.
    Asher NG; Olney AH; Schaefer GB
    Semin Pediatr Neurol; 2008 Dec; 15(4):221-3. PubMed ID: 19073332
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Congenital Hyposplenia with multiple additional anomalies: a variant of the Ivemark Syndrome].
    Nanan R; Wirbelauer J; Werner E; Schrod L; Speer CP
    Klin Padiatr; 2002; 214(5):299-302. PubMed ID: 12235547
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Biliary atresia splenic malformation syndrome--is it a result of embryonically midline rotational defects? A case report.
    Deveci MS; Deveci G
    J Pediatr Surg; 2000 Sep; 35(9):1377-80. PubMed ID: 10999706
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.