Genetics of tethered cord "syndrome": The FG syndrome

American Journal of Medical Genetics

Volumn 132 A, Issue 4, 2005, Pages 454-455

  Opitz, J M ^a  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CENTRAL NERVOUS SYSTEM DISEASE; CLINICAL FEATURE; COMORBIDITY; CONGENITAL MALFORMATION; DISEASE TRANSMISSION; GASTROINTESTINAL DISEASE; HUMAN; MENTAL RETARDATION MALFORMATION SYNDROME; NOTE; OPITZ SYNDROME; PLACENTA DISORDER; PRIORITY JOURNAL; RESPIRATORY TRACT DISEASE; TETHERED CORD SYNDROME; X CHROMOSOME LINKED DISORDER;

ABNORMALITIES, MULTIPLE; CHROMOSOME ABERRATIONS; GROWTH DISORDERS; HUMANS; MUSCLE HYPOTONIA; SPINAL DYSRAPHISM; SYNDROME;

EID: 12944266913     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30440     Document Type: Note

References (5)

1. Bianchi DW. 2000. Fetomaternal cell trafficking: A new cause of disease? Am J Med Genet 91:22-28.
2. Gottfried ON, Hedlund GL, Opitz JM, Walker ML. 2004. Chiari I malformation in patients with FG syndrome. Pediatr Neurosurg (in press).
3. Opitz JM, Kaveggia EG. 1974. Studies of malformation syndromes of man 33: The FG syndrome. An X-linked recessive syndrome of multiple congenital anomalies and mental retardation. Z Kinderheilkd 117(1):1-18.
4. Opitz JM, Rauch AM, Poss A, Peiffer A, Folland DS, Walker D. 2001. The FG syndrome: Perspective in 2001. Ital J Pediatr 27:715-729.
5. Ozonoff S, Williams BJ, Rauch AM, Opitz JO. 2000. Behavior phenotype of FG syndrome: Cognition, personality, and behavior in eleven affected boys. Am J Med Genet 97(2):112-118.