Paternally inherited deletion of CSH1 in a patient with Silver-Russell syndrome

Journal of Medical Genetics

Volumn 35, Issue 9, 1998, Pages 784-786

  Eggermann, Thomas ^a   Eggermann, Katja ^a   Mergenthaler, Susanne ^a   Kuner, Ruprecht ^a   Kaiser, Peter ^a   Ranke, Michael B ^a   Wollmann, Hartmut A ^a  

^a UNIVERSITY OF TÜBINGEN   (Germany)

Author keywords

Chorionic somatomammotrophin hormone 1 (CSH1); Growth hormone gene cluster; Silver Russell syndrome

Indexed keywords

HUMAN GROWTH HORMONE; PLACENTA LACTOGEN;

ARTICLE; CHILD; GENE CLUSTER; GENE DELETION; GROWTH RETARDATION; HUMAN; INFANT; MALE; PRIORITY JOURNAL; SILVER RUSSELL SYNDROME; UNIPARENTAL DISOMY;

EID: 0031869209     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.35.9.784     Document Type: Article

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