Comprehensive clinical studies in 34 patients with molecularly defined UPD(14)pat and related conditions (Kagami-Ogata syndrome)

European Journal of Human Genetics

Volumn 23, Issue 11, 2015, Pages 1488-1498

  Kagami, Masayo ^a   Kurosawa, Kenji ^b   Miyazaki, Osamu ^c   Ishino, Fumitoshi ^d   Matsuoka, Kentaro ^c   Ogata, Tsutomu ^a,e  

^a NATIONAL RESEARCH INSTITUTE FOR CHILD HEALTH AND DEVELOPMENT   (Japan)

^b KANAGAWA CHILDREN'S MEDICAL CENTER   (Japan)

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

^d TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

^e HAMAMATSU UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BECKWITH WIEDEMANN SYNDROME; BIRTH WEIGHT; CHEEK; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CLINICAL STUDY; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; FACIES; FEMALE; GENE DELETION; HEMOPHAGOCYTIC SYNDROME; HEPATOBLASTOMA; HUMAN; HYDRAMNIOS; INFANCY; INFANT; INFLUENZA; INTELLECTUAL IMPAIRMENT; INTELLIGENCE QUOTIENT; KAGAMI OGATA SYNDROME; MALE; MALFORMATION SYNDROME; NEONATAL RESPIRATORY DISTRESS SYNDROME; NEWBORN; OMPHALOCELE; PATERNAL UNIPARENTAL DISOMY14; PHILTRUM; PRIORITY JOURNAL; RESPIRATORY TRACT INFECTION; ROBERTSONIAN CHROMOSOME TRANSLOCATION; SURVIVAL RATE; THORAX RADIOGRAPHY; UNIPARENTAL DISOMY; ADOLESCENT; CHROMOSOME 14; CRANIOFACIAL MALFORMATION; GENETICS; GENOME IMPRINTING; GESTATIONAL AGE; KAPLAN MEIER METHOD; MULTIPLE MALFORMATION SYNDROME; PATHOPHYSIOLOGY; PREGNANCY; PRESCHOOL CHILD;

ABNORMALITIES, MULTIPLE; ADOLESCENT; BECKWITH-WIEDEMANN SYNDROME; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 14; CRANIOFACIAL ABNORMALITIES; DEVELOPMENTAL DISABILITIES; FEMALE; GENOMIC IMPRINTING; GESTATIONAL AGE; HUMANS; INFANT; INFANT, NEWBORN; INTELLECTUAL DISABILITY; KAPLAN-MEIER ESTIMATE; MALE; PREGNANCY; UNIPARENTAL DISOMY;

EID: 84944352498     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2015.13     Document Type: Article

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