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

151 related items for PubMed ID: 12624156

  • 1. Analphoid de novo marker chromosome inv dup(3)(q28qter) with neocentromere in a dysmorphic and developmentally retarded girl.
    Barbi G, Spaich C, Adolph S, Kehrer-Sawatzki H.
    J Med Genet; 2003 Mar; 40(3):e27. PubMed ID: 12624156
    [No Abstract] [Full Text] [Related]

  • 2. Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome.
    Levy B, Papenhausen P, Tepperberg J, Dunn T, Fallet S, Magid M, Kardon N, Hirschhorn K, Warburton P.
    Cytogenet Cell Genet; 2000 Mar; 91(1-4):165-70. PubMed ID: 11173851
    [Abstract] [Full Text] [Related]

  • 3. Stable dicentric duplication-deficiency chromosome 14 resulting from crossing-over within a maternal paracentric inversion.
    Lefort G, Blanchet P, Belgrade N, Rivier F, Chaze AM, Sarda P, Demaille J, Pellestor F.
    Am J Med Genet A; 2003 Apr 15; 118A(2):333-8. PubMed ID: 12698965
    [Abstract] [Full Text] [Related]

  • 4. Neocentromere marker chromosome of distal 3q mimicking dup(3q) syndrome phenotype.
    Izumi K, Yamashita Y, Aramaki M, Kosaki R, Hosokai N, Takahashi T, Kosaki K.
    Am J Med Genet A; 2008 Aug 01; 146A(15):1967-71. PubMed ID: 18561337
    [Abstract] [Full Text] [Related]

  • 5. Class II Analphoid Chromosome in a Child with Aberrant Chromosome 7: A Rare Cytogenetic Association.
    Kumar MJ, Kumar RA, Subhashree V, Jayasudha T, Hemagowri V, Koshy T, Gowrishankar K.
    Cytogenet Genome Res; 2015 Aug 01; 146(2):120-123. PubMed ID: 26226839
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Triplication of 15q11-q13 with inv dup(15) in a female with developmental delay.
    Long FL, Duckett DP, Billam LJ, Williams DK, Crolla JA.
    J Med Genet; 1998 May 01; 35(5):425-8. PubMed ID: 9610809
    [Abstract] [Full Text] [Related]

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

  • 12. Developmental delay caused by a supernumerary chromosome, inv dup (15), identified by fluorescent in situ hybridization.
    Abuelo D, Mark HF, Bier JA.
    Clin Pediatr (Phila); 1995 Apr 01; 34(4):223-6. PubMed ID: 7540523
    [No Abstract] [Full Text] [Related]

  • 13. Trisomy 20p resulting from inverted duplication and neocentromere formation.
    Voullaire L, Saffery R, Davies J, Earle E, Kalitsis P, Slater H, Irvine DV, Choo KH.
    Am J Med Genet; 1999 Aug 06; 85(4):403-8. PubMed ID: 10398268
    [Abstract] [Full Text] [Related]

  • 14. Supernumerary der(1) marker chromosome derived from a ring chromosome 1 which has retained the original centromere and euchromatin from 1q21.1 --> q21.3 with substantial loss of 1q12 heterochromatin in a female with dysmorphic features and psychomotoric developmental delay.
    Barbi G, Spaich Ch, Adolph S, Rossier E, Kehrer-Sawatzki H.
    Am J Med Genet A; 2005 Feb 01; 132A(4):419-24. PubMed ID: 15633178
    [Abstract] [Full Text] [Related]

  • 15. Mosaic inv dup(8p) marker chromosome with stable neocentromere suggests neocentromerization is a post-zygotic event.
    Voullaire L, Saffery R, Earle E, Irvine DV, Slater H, Dale S, du Sart D, Fleming T, Choo KH.
    Am J Med Genet; 2001 Jul 22; 102(1):86-94. PubMed ID: 11471179
    [Abstract] [Full Text] [Related]

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

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.