Maternal uniparental disomy 7 - Review and further delineation of the phenotype

European Journal of Pediatrics

Volumn 159, Issue 4, 2000, Pages 247-256

  Kotzot, D ^a   Balmer, D ^a   Baumer, A ^a   Chrzanowska, K ^b   Hamel, B C J ^c   Ilyina, H ^d   Krajewska Walasek, M ^b   Lurie, I W ^d   Otten, B J ^c   Schoenle, E ^a   Tariverdian, G ^e   Schinzel, A ^a  

^a UNIVERSITY OF ZURICH   (Switzerland)

^b CHILDREN'S MEMORIAL HEALTH INSTITUTE   (Poland)

^c RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^d BELARUSIAN STATE UNIVERSITY   (Belarus)

^e UNIVERSITY OF HEIDELBERG   (Germany)

Author keywords

Heterodisomy; Isodisomy; Maternal uniparental disomy 7; Mosaicism; Silver Russell syndrome

Indexed keywords

MICROSATELLITE DNA;

ADOLESCENT; ARTICLE; BONE MATURATION; CAFE AU LAIT SPOT; CHILD; CHORION VILLUS; CHROMOSOME 7; CHROMOSOME DISORDER; CLINICAL ARTICLE; CLINODACTYLY; FACE MALFORMATION; FEMALE; GROWTH RETARDATION; HEAD CIRCUMFERENCE; HUMAN; MALE; MEIOSIS; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; PSYCHOMOTOR DEVELOPMENT; SILVER RUSSELL SYNDROME; UNIPARENTAL DISOMY;

EID: 0034113750     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004310050064     Document Type: Article

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