Preferential paternal origin of microdeletions caused by prezygotic chromosome or chromatid rearrangements in Sotos syndrome

American Journal of Human Genetics

Volumn 72, Issue 5, 2003, Pages 1331-1337

  Miyake, Noriko ^a,d   Kurotaki, Naohiro ^a,d   Sugawara, Hirobumi ^a,e   Shimokawa, Osamu ^c   Harada, Naoki ^a,c,d   Kondoh, Tatsuro ^a   Tsukahara, Masato ^f   Ishikiriyama, Satoshi ^g   Sonoda, Tohru ^h   Miyoshi, Yoko ⁱ   Sakazume, Satoru ^j   Fukushima, Yoshimitsu ^j   Ohashi, Hirofumi ^k   Nagai, Toshiro ^l   Kawame, Hiroshi ^m   Kurosawa, Kenji ⁿ   Touyama, Mayumi ^o   Shiihara, Takashi ^e   Okamoto, Nobuhiko ^p   Nishimoto, Junji ^q   Yoshiura, Ko Ichiro ^a,d   Ohta, Tohru ^b,d   Kishino, Tatsuya ^b,d   Niikawa, Norio ^a,d   Matsumoto, Naomichi ^a,d   more..

^a NAGASAKI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b NAGASAKI UNIVERSITY   (Japan)

^c Kyushu Medical Science Nagasaki Laboratory   (Japan)

^d JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

^e YAMAGATA UNIVERSITY   (Japan)

^f YAMAGUCHI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^g CHIBA CHILDREN'S HOSPITAL   (Japan)

^h UNIVERSITY OF MIYAZAKI   (Japan)

ⁱ OSAKA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^j SHINSHU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^k SAITAMA CHILDREN'S MEDICAL CENTER   (Japan)

^l DOKKYO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^m NAGANO CHILDREN'S HOSPITAL   (Japan)

ⁿ KANAGAWA CHILDREN'S MEDICAL CENTER   (Japan)

^o JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

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

^q Kinki Central Hospital of Mutual Association of Public School Teachers   (Japan)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CANCER SUSCEPTIBILITY; CHROMATID; CHROMOSOME 5Q; CHROMOSOME MARKER; CHROMOSOME REARRANGEMENT; CLINICAL ARTICLE; CLINICAL FEATURE; DNA FLANKING REGION; FACE DYSMORPHIA; FEMALE; GENE DELETION; GENE LOCUS; GENE MAPPING; GENOTYPE; HAPLOTYPE; HUMAN; MALE; MENTAL DEFICIENCY; MICROSATELLITE MARKER; NUCLEOTIDE SEQUENCE; PATERNITY; POINT MUTATION; PRIORITY JOURNAL; SOTOS SYNDROME; ZYGOTE;

EID: 0038067733     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/375166     Document Type: Article

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