Do patients with maternal uniparental disomy for chromosome 7 have a distinct mild Silver-Russell phenotype? [12]

Journal of Medical Genetics

Volumn 38, Issue 4, 2001, Pages 273-278

  Hannula, K ^a   Kere, J ^a   Pirinen, S ^a   Holmberg, C ^a   Lipsanen Nyman, M ^a  

^a UNIVERSITY OF HELSINKI   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; CASE REPORT; CHROMOSOME 7; CLINICAL FEATURE; DEVELOPMENTAL DISORDER; DISEASE SEVERITY; FACE DYSMORPHIA; GENOTYPE; HUMAN; INTRAUTERINE GROWTH RETARDATION; LETTER; MALE; PHENOTYPE; PRIORITY JOURNAL; SHORT STATURE; SILVER RUSSELL SYNDROME; UNIPARENTAL DISOMY;

ADULT; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 7; DINUCLEOTIDE REPEATS; DNA; FAMILY HEALTH; FEMALE; GENOTYPE; GROWTH DISORDERS; HUMANS; INFANT; MALE; PHENOTYPE; SYNDROME;

EID: 0035058522     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

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34. Prader-Willi syndrome: Phenotypic differences observed in an objective study of deletion and disomy