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 *

202 related articles for article (PubMed ID: 7424976)

  • 1. Hallux duplication, postaxial polydactyly, absence of the corpus callosum, severe mental retardation, and additional anomalies in two unrelated patients: a new syndrome.
    Schinzel A; Schmid W
    Am J Med Genet; 1980; 6(3):241-9. PubMed ID: 7424976
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The acrocallosal syndrome.
    Nelson MM; Thomson AJ
    Am J Med Genet; 1982 Jun; 12(2):195-9. PubMed ID: 7102724
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Postaxial polydactyly, hallux duplication, absence of the corpus callosum, macrencephaly and severe mental retardation: a new syndrome?
    Schinzel A
    Helv Paediatr Acta; 1979 May; 34(2):141-6. PubMed ID: 457430
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Acrocallosal syndrome in a girl born to consanguineous parents.
    Salgado LJ; Ali CA; Castilla EE
    Am J Med Genet; 1989 Mar; 32(3):298-300. PubMed ID: 2729348
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [The acrocallosal syndrome. Report of an additional case].
    Wendisch J; Lorenz P; Kabus M; Rupprecht E; Walther S
    Kinderarztl Prax; 1990 Jun; 58(6):315-21. PubMed ID: 2166860
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hypogenitalism in the acrocallosal syndrome.
    Temtamy SA; Meguid NA
    Am J Med Genet; 1989 Mar; 32(3):301-5. PubMed ID: 2658583
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Triplets with growth failure, microcephaly, mental retardation, nail hypoplasia and corpus callosum agenesis: is it a variant of Coffin-Siris or a new syndrome?
    Kirel B; Kural N; Yakut A; Adapinar B
    Turk J Pediatr; 2000; 42(2):171-6. PubMed ID: 10936989
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Greig cephalopolysyndactyly syndrome with dysgenesis of the corpus callosum in a Bedouin family.
    Marafie MJ; Temtamy SA; Rajaram U; al-Awadi SA; el-Badramany MH; Farag TI
    Am J Med Genet; 1996 Dec; 66(3):261-4. PubMed ID: 8985483
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Filippi syndrome: report of three additional cases.
    Williams MS; Williams JL; Wargowski DS; Pauli RM; Pletcher BA
    Am J Med Genet; 1999 Nov; 87(2):128-33. PubMed ID: 10533026
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An additional manifestation in acrocallosal syndrome: temporal lobe hypoplasia.
    Aykut A; Cogulu O; Ekmekci AY; Ozkinay F
    Genet Couns; 2008; 19(2):237-40. PubMed ID: 18618999
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Acrocallosal syndrome in a child with de novo inverted tandem duplication of 12p11.2-p13.3.
    Pfeiffer RA; Legat G; Trautmann U
    Ann Genet; 1992; 35(1):41-6. PubMed ID: 1610119
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Acrocallosal syndrome in fetus: focus on additional brain abnormalities.
    Fernandez C; Soulier M; Coulibaly B; Liprandi A; Benoit B; Giuliano F; Sigaudy S; Figarella-Branger D; Fallet-Bianco C
    Acta Neuropathol; 2008 Jan; 115(1):151-6. PubMed ID: 17593378
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Callosal defect, microcephaly, severe mental retardation, and other anomalies in three sibs.
    da-Silva EO
    Am J Med Genet; 1988 Apr; 29(4):837-43. PubMed ID: 3400727
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Craniosynostosis, agenesis of the corpus callosum, serve mental retardation, distinctive facies, camptodactyly, and hypogonadism.
    Lin AE; Gettig E
    Am J Med Genet; 1990 Apr; 35(4):582-5. PubMed ID: 2333890
    [No Abstract]   [Full Text] [Related]  

  • 15. [Agenesis of the corpus callosum].
    Nielsen LH
    Ugeskr Laeger; 1995 Feb; 157(6):737-9. PubMed ID: 7701633
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Thrombocytopenia-absent radius (tar) syndrome: a case with agenesis of corpus callosum, hypoplasia of cerebellar vermis and horseshoe kidney.
    Skórka A; Bielicka-Cymermann J; Gieruszczak-Białek D; Korniszewski L
    Genet Couns; 2005; 16(4):377-82. PubMed ID: 16440880
    [TBL] [Abstract][Full Text] [Related]  

  • 17. New autosomal recessive multiple congenital abnormalities/mental retardation syndrome with craniofacial dysmorphism absent corpus callosum, iris colobomas and connective tissue dysplasia.
    Temtamy SA; Salam MA; Aboul-Ezz EH; Hussein HA; Helmy SA; Shalash BA
    Clin Dysmorphol; 1996 Jul; 5(3):231-40. PubMed ID: 8818452
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Delineation of the da-Silva syndrome.
    Naritomi K; Tohma T; Goya Y; Shiroma N; Hirayama K
    Am J Med Genet; 1994 Feb; 49(3):313-6. PubMed ID: 8209892
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Possible new autosomal recessive syndrome of partial agenesis of the corpus callosum, pontine hypoplasia, focal white matter changes, hypotonia, mental retardation, and minor anomalies.
    Jonas RE; Kimonis VE; Morales A
    Am J Med Genet; 1997 Dec; 73(2):184-8. PubMed ID: 9409870
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly. A new syndrome?
    Filippi G
    Am J Med Genet; 1985 Dec; 22(4):821-4. PubMed ID: 4073130
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.