Cytogenetic and molecular-cytogenetic investigation of Rett syndrome: Analysis of 31 cases

NeuroReport

Volumn 8, Issue 1, 1997, Pages 187-189

  Vorsanova, S G ^a,b   Demidova, I A ^a   Ulas, V Yu ^a   Soloviev, I V ^b,c   Kazantzeva, L Z ^b   Yurov, Yu B ^b,c  

^a PIROGOV RUSSIAN NATIONAL RESEARCH MEDICAL UNIVERSITY   (Russian Federation)

^b CNRS   (France)

^c INSTITUTE OF BIOMEDICAL CHEMISTRY   (Russian Federation)

Author keywords

Abnormal karyotype; Fluorescence in situ hybridization; Fragile site; Rett Syndrome; X chromosomes

Indexed keywords

ARTICLE; CONTROLLED STUDY; FEMALE; HUMAN; HUMAN CELL; HUMAN TISSUE; IN SITU HYBRIDIZATION; MALE; PRIORITY JOURNAL; RETT SYNDROME; X CHROMOSOME;

EID: 0030937663     PISSN: 09594965     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001756-199612200-00038     Document Type: Article

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