Microarray analysis of 50 patients reveals the critical chromosomal regions responsible for 1p36 deletion syndrome-related complications

Brain and Development

Volumn 37, Issue 5, 2015, Pages 515-526

  Shimada, Shino ^a   Shimojima, Keiko ^a   Okamoto, Nobuhiko ^b   Sangu, Noriko ^a   Hirasawa, Kyoko ^a   Matsuo, Mari ^a   Ikeuchi, Mayo ^c   Shimakawa, Shuichi ^d   Shimizu, Kenji ^e   Mizuno, Seiji ^f   Kubota, Masaya ^g   Adachi, Masao ^h   Saito, Yoshiaki ⁱ   Tomiwa, Kiyotaka ^j   Haginoya, Kazuhiro ^k   Numabe, Hironao ^l   Kako, Yuko ^m   Hayashi, Ai ⁿ   Sakamoto, Haruko ^o   Hiraki, Yoko ^p   Minami, Koichi ^q   Takemoto, Kiyoshi ^r   Watanabe, Kyoko ^s   Miura, Kiyokuni ^t   Chiyonobu, Tomohiro ^u   Kumada, Tomohiro ^v   Imai, Katsumi ^w   Maegaki, Yoshihiro ^x   Nagata, Satoru ^a   Kosaki, Kenjiro ^y   Izumi, Tatsuro ^c   Nagai, Toshiro ^z   Yamamoto, Toshiyuki ^a   more..

^a TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

^b RESEARCH INSTITUTE FOR MATERNAL AND CHILD HEALTH   (Japan)

^c OITA UNIVERSITY   (Japan)

^d OSAKA MEDICAL COLLEGE   (Japan)

^e SAITAMA CHILDREN'S MEDICAL CENTER   (Japan)

^f INSTITUTE FOR DEVELOPMENTAL RESEARCH   (Japan)

^g NATIONAL CENTER FOR CHILD HEALTH AND DEVELOPMENT   (Japan)

^h Kakogawa West City Hospital   (Japan)

ⁱ NATIONAL INSTITUTE OF MENTAL HEALTH   (Japan)

^j OSAKA CITY GENERAL HOSPITAL   (Japan)

^k Takuto Rehabilitation Center for Children   (Japan)

^l OCHANOMIZU UNIVERSITY   (Japan)

^m SHOWA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

ⁿ KYOTO FIRST RED CROSS HOSPITAL   (Japan)

^o OSAKA RED CROSS HOSPITAL   (Japan)

^p Hiroshima Municipal Center for Child Health and Development   (Japan)

^q WAKAYAMA MEDICAL UNIVERSITY   (Japan)

^r Osaka Developmental Rehabilitation Center   (Japan)

^s Kokura Medical Center   (Japan)

^t NAGOYA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^u KYOTO PREFECTURAL UNIVERSITY OF MEDICINE   (Japan)

^v SHIGA MEDICAL CENTER FOR CHILDREN   (Japan)

^w SHIZUOKA INSTITUTE OF EPILEPSY AND NEUROLOGICAL DISORDERS   (Japan)

^x TOTTORI UNIVERSITY   (Japan)

^y KEIO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^z DOKKYO MEDICAL UNIVERSITY   (Japan)

more..

Author keywords

1p36 deletion syndrome; Ambulation; Chromosomal deletion; Distinctive features; Epilepsy; Genotype phenotype correlation; Intellectual disability

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BLOOD SAMPLING; CHILD; CHROMOSOME DELETION; CLINICAL ARTICLE; CLINICAL FEATURE; COPY NUMBER VARIATION; CYTOGENETICS; EPILEPSY; FEMALE; GENOTYPE PHENOTYPE CORRELATION; HEART DISEASE; HUMAN; INTELLECTUAL IMPAIRMENT; JAPAN; MALE; MICROARRAY ANALYSIS; MONOSOMY 1P36 SYNDROME; MOSAICISM; CHROMOSOME 1; CHROMOSOME DISORDERS; COMPLICATION; GENETIC ASSOCIATION; GENETICS; INFANT; NEWBORN; PRESCHOOL CHILD; PROCEDURES; YOUNG ADULT;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 1; FEMALE; GENETIC ASSOCIATION STUDIES; HUMANS; INFANT; INFANT, NEWBORN; JAPAN; MALE; MICROARRAY ANALYSIS; YOUNG ADULT;

EID: 84925272911     PISSN: 03877604     EISSN: 18727131     Source Type: Journal    
DOI: 10.1016/j.braindev.2014.08.002     Document Type: Article

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