Published in Am J Hum Genet on November 01, 1996
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Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome. Eur J Hum Genet (2014) 0.84
Translocation breakpoint in two unrelated Tourette syndrome cases, within a region previously linked to the disorder. Hum Genet (2003) 0.81
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The D2 dopamine receptor gene as a determinant of reward deficiency syndrome. J R Soc Med (1996) 1.98
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Detection of major gene for Gilles de la Tourette syndrome. Am J Hum Genet (1984) 1.54
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Hemizygosity of delta-catenin (CTNND2) is associated with severe mental retardation in cri-du-chat syndrome. Genomics (2000) 1.47
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The mechanism of C- and G-banding of chromosomes. Exp Cell Res (1973) 1.38
A fine structure physical map of the short arm of chromosome 5. Am J Hum Genet (1986) 1.35
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Clinical and molecular characterisation of 80 patients with 5p deletion: genotype-phenotype correlation. J Med Genet (2001) 1.26
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Partial deletion of chromosome 6p: delineation of the syndrome. Am J Med Genet (1991) 1.22
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Molecular cloning and mapping of human semaphorin F from the Cri-du-chat candidate interval. Biochem Biophys Res Commun (1998) 1.21
Analysis of clinical variation seen in patients with 18q terminal deletions. Am J Med Genet (1995) 1.16
Optical Studies of the interaction of 4'-6'-diamidino-2-phenylindole with DNA and metaphase chromosomes. Chromosoma (1977) 1.16
Somatic cell hybrid deletion map of human chromosome 18. Genomics (1992) 1.15
Dopamine receptor genes are associated with age at first sexual intercourse. J Biosoc Sci (1999) 1.14
Evidence for a distinct region causing a cat-like cry in patients with 5p deletions. Am J Hum Genet (1995) 1.13
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Tourette syndrome: clinical and psychological aspects of 250 cases. Am J Hum Genet (1985) 1.13
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Five novel genes from the cri-du-chat critical region isolated by direct selection. Hum Mol Genet (1995) 1.02
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Duplication 3q syndrome: molecular delineation of the critical region. Am J Med Genet (1995) 1.00
The structural genes, MEP1A and MEP1B, for the alpha and beta subunits of the metalloendopeptidase meprin map to human chromosomes 6p and 18q, respectively. Genomics (1995) 1.00
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Tourette's syndrome and attention deficit disorder with hyperactivity: are they genetically related? J Am Acad Child Psychiatry (1984) 0.99
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Characterization of a complex chromosomal rearrangement in a patient with a typical catlike cry and no other clinical findings of cri-du-chat syndrome. Am J Med Genet (1999) 0.97
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Physical mapping of genetic markers on the short arm of chromosome 5. Genomics (1994) 0.96
A case of familial exhibitionism in Tourette's syndrome successfully treated with haloperidol. Am J Psychiatry (1982) 0.94
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Neuropsychiatry of 18q- syndrome. Am J Med Genet (1996) 0.92
Clinical and molecular evaluation of four patients with partial duplications of the long arm of chromosome 18. Am J Hum Genet (1993) 0.92
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A new deletion of 18q23 with few typical features of the 18q- syndrome. J Med Genet (1996) 0.87
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