Reverse mutation in fragile X syndrome [1]

American Journal of Human Genetics

Volumn 58, Issue 1, 1996, Pages 237-239

  Antinolo, G ^a   Borrego, S ^a   Cabeza, J C ^a   Sanchez, R ^a   Sanchez, J ^a   Sanchez, B ^a  

^a HOSPITAL UNIVERSITARIO VIRGEN DEL ROCÍO   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE TRANSMISSION; DNA HYBRIDIZATION; FAMILIAL DISEASE; FEMALE; FRAGILE X SYNDROME; GENE ISOLATION; HUMAN; KARYOTYPE; LETTER; MOSAICISM; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; REVERTANT;

CASE REPORT; DISEASES IN TWINS; FEMALE; FRAGILE X SYNDROME; HUMAN; INCIDENCE; MALE; MUTATION; PEDIGREE; PHENOTYPE; REPETITIVE SEQUENCES, NUCLEIC ACID; RESTRICTION MAPPING; X CHROMOSOME;

EID: 0029655386     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

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