Mild phenotype associated with inv dup 8 (q21.2-q22.3) of maternal origin

American Journal of Medical Genetics

Volumn 62, Issue 2, 1996, Pages 160-163

  Tupler, Rossella ^a,b   Pagliano, Emanuela ^a   Barbierato, Laura ^a   Lanzi, Giovanni ^a   Maraschio, Paola ^a   Fazzi, Elisa ^a  

^a UNIVERSITY OF PAVIA   (Italy)

^b Biologia Generale e Genetica Medica   (Italy)

Author keywords

flat nasal bridge; high arched palate; maternal origin; micrognathia; mild mental retardation; trisomy 8q21.2 q22.3; umbilical hernia

Indexed keywords

ARTICLE; CASE REPORT; CAVERNOUS HEMANGIOMA; CHILD; CHROMOSOME 8; CHROMOSOME DUPLICATION; CHROMOSOME INVERSION; CHROMOSOME REARRANGEMENT; CYTOGENETICS; FEMALE; GENOTYPE; HUMAN; HYPERTELORISM; MICROGNATHIA; MUSCLE HYPOTONIA; NOSE MALFORMATION; PALATE MALFORMATION; PHENOTYPE; PRIORITY JOURNAL; TRISOMY 8; UMBILICAL HERNIA;

EID: 0029872879     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1096-8628(19960315)62:2<160::aid-ajmg8>3.0.co;2-#     Document Type: Article

References (6)

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