Preimplantation genetic diagnosis for severe albright hereditary osteodystrophy

Journal of Clinical Endocrinology and Metabolism

Volumn 93, Issue 3, 2008, Pages 901-904

  Lietman, Steven A ^a   Goldfarb, James ^a   Desai, Nina ^a   Levine, Michael A ^a  

^a LERNER RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALBRIGHT SYNDROME; ARTICLE; CONTROLLED STUDY; DISEASE SEVERITY; EMBRYO; FAMILY HISTORY; FEMALE; FERTILIZATION IN VITRO; GENE; GENE MUTATION; GENE SEQUENCE; GNAS GENE; HUMAN; HUMAN CELL; MALE; PHENOTYPE; PHOCOMELIA; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; PSEUDOHYPOPARATHYROIDISM;

EID: 40849137683     PISSN: 0021972X     EISSN: 0021972X     Source Type: Journal    
DOI: 10.1210/jc.2007-2040     Document Type: Article

References (20)

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