Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): A gene causing neuronal migration defects in human brain

Human Molecular Genetics

Volumn 6, Issue 4, 1997, Pages 555-562

  Ross, M Elizabeth ^a   Allen, Kristina M ^b   Srivastava, Anand K ^c   Featherstone, Terry ^d   Gleeson, Joseph G ^b   Hirsch, Betsy ^a   Harding, Brian N ^e   Andermann, Eva ^f   Abdullah, Rabi ^b   Berg, Michael ^g   Czapansky Bielman, Désirée ^a   Flanders, Dean J ^h   Guerrini, Renzo ⁱ   Motté, Jacques ^j   Mira, A Puche ^k   Scheffer, Ingrid ^l   Berkovic, Samuel ^l   Scaravilli, F ^m   King, Richard A ^h   Ledbetter, David H ⁿ   Schlessinger, David ^d   Dobyns, William B ^a   Walsh, Christopher A ^b   more..

^a UNIV OF MINNESOTA HOSP AND CLINIC   (United States)

^b HARVARD UNIVERSITY   (United States)

^c GREENWOOD GENETIC CENTER   (United States)

^d WASHINGTON UNIVERSITY   (United States)

^e HOSPITAL FOR SICK CHILDREN   (United Kingdom)

^f MCGILL UNIVERSITY   (Canada)

^g UNIVERSITY OF ROCHESTER MEDICAL CENTER   (United States)

^h UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

ⁱ UNIVERSITY OF PISA   (Italy)

^j AMERICAN MEMORIAL HOSPITAL   (France)

^k HOSPITAL UNIVERSITARIO VIRGEN DE LA ARRIXACA   (Spain)

^l AUSTIN HOSPITAL   (Australia)

^m Neuropathology Natl Hosp N   (United Kingdom)

ⁿ UNIVERSITY OF CHICAGO   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

AGYRIA; ARTICLE; BRAIN DEVELOPMENT; CELL MIGRATION; CHROMOSOME 2; CHROMOSOME ANALYSIS; CHROMOSOME TRANSLOCATION; CHROMOSOME XQ; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE FUNCTION; GENE MAPPING; GENETIC LINKAGE; HUMAN; HUMAN CELL; HYBRID CELL; MALE; MARKER GENE; NERVOUS SYSTEM DEVELOPMENT; PRIORITY JOURNAL; X CHROMOSOME LINKAGE;

CEREBRAL CORTEX; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 2; DOSAGE COMPENSATION, GENETIC; EPILEPSY; FEMALE; HUMANS; HYBRID CELLS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; LINKAGE (GENETICS); MALE; PEDIGREE; PHENOTYPE; RESTRICTION MAPPING; SEX CHROMOSOME ABERRATIONS; TRANSLOCATION, GENETIC; X CHROMOSOME;

EID: 8244247118     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/6.4.555     Document Type: Article

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