Interstitial 1q25.3-q31.3 Deletion in a Boy with Mild Manifestations

American Journal of Medical Genetics

Volumn 123 A, Issue 3, 2003, Pages 290-295

  Höglund, Pia ^a,b,c   Jalkanen, Reetta ^b   Marttinen, Eino ^a   Alitalo, Tiina ^b  

^a UNIVERSITY OF HELSINKI   (Finland)

^b HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

^c HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

Author keywords

1q25.3 q31.3; Chromosome 1; Interstitial deletion; Review

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHROMOSOME; CHROMOSOME 1; CHROMOSOME 1Q; CHROMOSOME 25; CHROMOSOME 35Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME MARKER; CHROMOSOME Q BAND; CHROMOSOME SATELLITE ASSOCIATION; CLINICAL FEATURE; CRYPTORCHISM; DISEASE SEVERITY; EAR MALFORMATION; HUMAN; HUMAN CELL; INHERITANCE; LYMPHOCYTE; MALE; MENTAL DEFICIENCY; MICROGNATHIA; PATERNAL INHERITANCE; PRIORITY JOURNAL; SPEECH DISORDER; THUMB MALFORMATION; TOE MALFORMATION;

EID: 0345327689     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.20385     Document Type: Article

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