A Syndrome with Multiple Malformations, Mental Retardation, and ACTH Deficiency

American Journal of Medical Genetics

Volumn 126 A, Issue 3, 2004, Pages 313-318

  Kajantie, Eero ^a,b   Otonkoski, Timo ^a   Kivirikko, Sirpa ^b   Somer, Mirja ^b,c  

^a HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

^b HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

^c UNIVERSITY OF HELSINKI   (Finland)

Author keywords

Adrenal insufficiency; Cortisol; Seckel syndrome; Smith Lemli Opitz syndrome; Toriello Carey syndrome

Indexed keywords

ADRENAL INSUFFICIENCY; ARTICLE; CASE REPORT; CHILD; CLEFT PALATE; CORTICOTROPIN DEFICIENCY; FAMILY HISTORY; GROWTH RETARDATION; HEARING LOSS; HEART ATRIUM SEPTUM DEFECT; HUMAN; HYPOSPADIAS; MALE; MENTAL RETARDATION MALFORMATION SYNDROME; MICROCEPHALY; MICROGNATHIA; MULTIPLE MALFORMATION SYNDROME; PRIORITY JOURNAL; SECKEL SYNDROME; SKELETON MALFORMATION; SMITH LEMLI OPITZ SYNDROME;

ERETMOCHELYS IMBRICATA;

EID: 1842458426     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.20604     Document Type: Article

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