Two further AHO-like syndrome patients with deletion of glypican 1 gene region in 2q37.2-q37.3.

International journal of molecular medicine

Volumn 14, Issue 6, 2004, Pages 977-979

  Polityko, Anna ^a   Maltseva, Olga ^a   Rumyantseva, Natalia ^a   Khurs, Olga ^a   Seidel, Jörg ^a   Claussen, Uwe ^a   Weise, Anja ^a   Liehr, Thomas ^a   Starke, Heike ^a  

^a Institute of Human Genetics and Anthropology   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEOHEPARAN SULFATE;

ADULT; ALBRIGHT SYNDROME; ARTICLE; CASE REPORT; CHILD; CHROMOSOME 2; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENETICS; HUMAN; MALE; PATHOLOGY;

ADULT; CHILD; CHROMOSOMES, HUMAN, PAIR 2; FEMALE; FIBROUS DYSPLASIA, POLYOSTOTIC; GENE DELETION; HEPARAN SULFATE PROTEOGLYCANS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE;

MLCS; MLOWN;

EID: 21644457768     PISSN: 11073756     EISSN: None     Source Type: Journal    
DOI: 10.3892/ijmm.14.6.977     Document Type: Article

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