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Brain and Development

Volumn 23, Issue SUPPL. 1, 2001, Pages

Molecular-cytogenetic investigation of skewed chromosome X inactivation in Rett syndrome

(4) Yurov, Yuri B a Vorsanova, Svetlana G b Kolotii, Alexei D b Iourov, Ivan Y a

a INSTITUTE OF BIOMEDICAL CHEMISTRY (Russian Federation)

b N N BLOKHIN NATIONAL MEDICAL RESEARCH CENTER OF ONCOLOGY (Russian Federation)

Author keywords

Chromosomal heteromorphism; Fluorescence in situ hybridization; Rett syndrome; Skewed X inactivation

Indexed keywords

FLUORESCENT DYE; SATELLITE DNA;

CONFERENCE PAPER; CONTROLLED STUDY; DNA PROBE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN TISSUE; INTERPHASE; MAJOR CLINICAL STUDY; RETT SYNDROME; X CHROMOSOME; X CHROMOSOME INACTIVATION;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; DOSAGE COMPENSATION, GENETIC; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INFANT, NEWBORN; LYMPHOCYTES; MUTATION; RETT SYNDROME; X CHROMOSOME;

EID: 0035194286 PISSN: 03877604 EISSN: None Source Type: Journal
DOI: 10.1016/S0387-7604(01)00370-9 Document Type: Conference Paper

Times cited : (10)

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