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Connection

T. Conrad Gilliam to Cloning, Molecular

This is a "connection" page, showing publications T. Conrad Gilliam has written about Cloning, Molecular.
Connection Strength

0.355
  1. Progress toward cloning of the gene responsible for childhood spinal muscular atrophy. Semin Neurol. 1993 Sep; 13(3):276-82.
    View in: PubMed
    Score: 0.108
  2. Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndrome. Cytogenet Genome Res. 2004; 107(1-2):68-76.
    View in: PubMed
    Score: 0.055
  3. Isolation of multiple genomic sequences coding for chicken myosin heavy chain protein. J Biol Chem. 1982 Jan 10; 257(1):549-56.
    View in: PubMed
    Score: 0.048
  4. Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictions. Hum Mol Genet. 1994 Sep; 3(9):1647-56.
    View in: PubMed
    Score: 0.029
  5. Mapping psychiatric disease genes: impact of new molecular strategies. J Psychiatr Res. 1992 Oct; 26(4):309-26.
    View in: PubMed
    Score: 0.025
  6. A DNA segment encoding two genes very tightly linked to Huntington's disease. Science. 1987 Nov 13; 238(4829):950-2.
    View in: PubMed
    Score: 0.018
  7. Isolation of polymorphic DNA fragments from human chromosome 4. Nucleic Acids Res. 1987 Feb 25; 15(4):1445-58.
    View in: PubMed
    Score: 0.017
  8. Positional cloning and characterisation of the human DLGAP2 gene and its exclusion in progressive epilepsy with mental retardation. Eur J Hum Genet. 2000 May; 8(5):381-4.
    View in: PubMed
    Score: 0.011
  9. Cloning and genomic organization of beclin 1, a candidate tumor suppressor gene on chromosome 17q21. Genomics. 1999 Jul 01; 59(1):59-65.
    View in: PubMed
    Score: 0.010
  10. Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3. Genomics. 1998 Mar 01; 48(2):171-7.
    View in: PubMed
    Score: 0.009
  11. Heterologous expression of the metal-binding domains of human copper-transporting ATPases (P1-ATPases). Ann N Y Acad Sci. 1997 Nov 03; 834:155-7.
    View in: PubMed
    Score: 0.009
  12. Chromosome jumping from D4S10 (G8) toward the Huntington disease gene. Proc Natl Acad Sci U S A. 1988 Sep; 85(17):6437-41.
    View in: PubMed
    Score: 0.005
  13. Molecular genetics of human chromosome 4. J Med Genet. 1986 Jun; 23(3):193-9.
    View in: PubMed
    Score: 0.004
  14. DNA markers for nervous system diseases. Science. 1984 Sep 21; 225(4668):1320-6.
    View in: PubMed
    Score: 0.004
  15. The implications of genetic variation in human pathology. Biochem Soc Symp. 1984; 49:183-8.
    View in: PubMed
    Score: 0.003
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.