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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

161 related items for PubMed ID: 6787562

  • 1. [Holoprosencephaly and agenesis of the corpus callosum. Contribution to the study of dysrhaphic states].
    Cincinnati P, Baciocco A, Sorano V, Lapresa M, Lalli F.
    Pediatria (Napoli); 1980 Jun 30; 88(2):229-47. PubMed ID: 6787562
    [No Abstract] [Full Text] [Related]

  • 2. Cerebral midline developmental anomalies: spectrum and associated features.
    Delezoide AL, Narcy F, Larroche JC.
    Genet Couns; 1990 Jun 30; 1(3-4):197-210. PubMed ID: 2098044
    [Abstract] [Full Text] [Related]

  • 3. [Agenesis of the corpus callosum].
    Antonenko VG, Robak OP.
    Zh Vopr Neirokhir Im N N Burdenko; 1980 Jun 30; (4):59-60. PubMed ID: 7424326
    [Abstract] [Full Text] [Related]

  • 4. Analysis of the gross anatomical variations found in four cases of trisomy 13.
    Colacino SC, Pettersen JC.
    Am J Med Genet; 1978 Jun 30; 2(1):31-50. PubMed ID: 122447
    [Abstract] [Full Text] [Related]

  • 5. Lipoma of corpus callosum associated with dysraphic lesions and trisomy 13.
    Wainwright H, Bowen R, Radcliffe M.
    Am J Med Genet; 1995 May 22; 57(1):10-3. PubMed ID: 7645586
    [Abstract] [Full Text] [Related]

  • 6. [Partial agenesis of the corpus callosum with multiple ocular abnormalities and exceptional chromosome aberration].
    Ardouin M, Urvoy M, Le Marec B, Lessard M, Senecal J.
    Rev Otoneuroophtalmol; 1974 May 22; 46(2):143-7. PubMed ID: 4215115
    [No Abstract] [Full Text] [Related]

  • 7. [Cerebral malformation in the newborn: holoprosencephaly and agenesis of the corpus callosum].
    Alfonso I, Papazian O, Sinisterra S.
    Rev Neurol; 1974 May 22; 36(2):179-84. PubMed ID: 12589607
    [Abstract] [Full Text] [Related]

  • 8. Corpus callosum agenesis in trisomy 8p11.23 and monosomy 4q34 because of maternal translocation.
    Işik U, Başaran S, Dehgan T, Apak M.
    Pediatr Neurol; 2008 Jul 22; 39(1):55-7. PubMed ID: 18555175
    [Abstract] [Full Text] [Related]

  • 9. [The Arnold-Chiari malformation in the frame of the dysrhaphic equivalents of the cerebrum and the cerebellum. A contribution to the Durand-Zunin syndrome].
    David E, Müller K.
    Z Kinderheilkd; 1966 Feb 18; 95(3):263-90. PubMed ID: 4864046
    [No Abstract] [Full Text] [Related]

  • 10. Genetic counselling in holoprosencephaly.
    Burck U.
    Helv Paediatr Acta; 1982 Jun 18; 37(3):231-7. PubMed ID: 7118555
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Craniofacial abnormalities, agenesis of the corpus callosum, polysyndactyly and abnormal skin and gut development--the Curry Jones syndrome.
    Temple IK, Eccles DM, Winter RM, Baraitser M, Carr SB, Shortland D, Jones MC, Curry C.
    Clin Dysmorphol; 1995 Apr 18; 4(2):116-29. PubMed ID: 7606318
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. [Holoprosencephaly and agenesis of the corpus callosum. Contribution to the study of dysraphia].
    Baciocco A, Cincinnati P, Lapresa M, Sorano V, Lalli F.
    Riv Neurobiol; 1978 Apr 18; 24(4):311-23. PubMed ID: 388599
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. [Distal trisomy 14q associated with agenesis of the corpus callosus and truncus arteriosus due to the maternal translocation t(5;14)(q13;q23q32) (author's transl)].
    Geormaneanu M, Geormaneanu C, Walter-Rosianu A, Papuc M.
    Ann Genet; 1981 Apr 18; 24(3):176-8. PubMed ID: 6974531
    [No Abstract] [Full Text] [Related]

  • 18. Clinical, neuroimaging and cytogenetic findings in 20 patients with corpus callosum dysgenesis.
    dos Santos AC, Midleton SR, Fonseca RL, dos Santos SR, Llerena JC, Vargas FR.
    Arq Neuropsiquiatr; 2002 Jun 18; 60(2-B):382-5. PubMed ID: 12131936
    [Abstract] [Full Text] [Related]

  • 19. "Holoprosencephaly-polydactyly" (pseudotrisomy 13) syndrome: expansion of the phenotypic spectrum.
    Lurie IW, Wulfsberg EA.
    Am J Med Genet; 1993 Sep 01; 47(3):405-9. PubMed ID: 8135289
    [Abstract] [Full Text] [Related]

  • 20. Partial trisomy 1(q25qter) due to a de novo unbalanced 1;19 translocation in a neonate.
    Senses DA, Silan F, Uzun H, Zafer C, Ucar-Cavusoglu E, Kocabay K.
    Genet Couns; 2007 Sep 01; 18(4):409-16. PubMed ID: 18286822
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.