Narrowing the candidate region of Albright hereditary osteodystrophy-like syndrome by deletion mapping in a patient with an unbalanced cryptic translocation t(2;6)(q37.3;q26)

American Journal of Medical Genetics

Volumn 122 A, Issue 3, 2003, Pages 261-265

  Giardino, Daniela ^a   Finelli, Palma ^a,b   Gottardi, Giulietta ^a   De Canal, Gabriella ^a   Della Monica, Matteo ^c   Lonardo, Fortunato ^c   Scarano, Gioacchino ^c   Larizza, Lidia ^a,b  

^a ISTITUTO AUXOLOGICO ITALIANO   (Italy)

^b UNIVERSITY OF MILAN   (Italy)

^c G RUMMO HOSPITAL   (Italy)

Author keywords

2qter deletion; 6q partial trisomy; AHO like syndrome; Candidate gene region

Indexed keywords

ALBRIGHT HEREDITARY OSTEODYSTROPHY LIKE SYNDROME; ALBRIGHT SYNDROME; ARTICLE; BRACHYDACTYLY; CASE REPORT; CHILD; CHROMOSOME 2Q; CHROMOSOME 6Q; CHROMOSOME TRANSLOCATION; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE MAPPING; HUMAN; KARYOTYPE 46,XY; MALE; MENTAL DEFICIENCY; MONOSOMY; OBESITY; PHENOTYPE; PRIORITY JOURNAL; SHORT STATURE;

EID: 0141857855     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.20287     Document Type: Article

References (17)

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