Large deletion at the TSC1 locus in a family with tuberous sclerosis complex

Genetic Testing

Volumn 9, Issue 3, 2005, Pages 226-230

  Nellist, M ^a   Sancak, O ^a   Goedbloed, M A ^a   Van Veghel Plandsoen, M ^a   Maat Kievit, A ^a   Lindhout, D ^b   Bussen, B H ^a   De Klein, A ^a   Halley, D J J ^a   Van Den Ouweland, A M W ^a  

^a ERASMUS MEDICAL CENTER   (Netherlands)

^b UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 16P; CHROMOSOME 9Q; GENE; GENE DELETION; GENE LOCUS; GENE MUTATION; GENETIC SCREENING; HAMARTOMA; HUMAN; HUMAN CELL; MENTAL DEFICIENCY; MULTIGENE FAMILY; SEIZURE; TSC1 GENE; TSC2 GENE; TUBEROUS SCLEROSIS;

BASE SEQUENCE; DNA PRIMERS; FEMALE; GENE DELETION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MUTATION; PEDIGREE; TUBEROUS SCLEROSIS; TUMOR SUPPRESSOR PROTEINS;

EID: 27144445858     PISSN: 10906576     EISSN: None     Source Type: Journal    
DOI: 10.1089/gte.2005.9.226     Document Type: Article

References (13)

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