FG syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "FG syndrome" in English language version.

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Opitz JM, Kaveggia EG (1974). "Studies of malformation syndromes of man XXXIII: the FG syndrome. An X-linked recessive syndrome of multiple congenital anomalies and mental retardation". Z Kinderheilkd. 117 (1): 1–18. doi:10.1007/BF00439020. PMID 4365204. S2CID 25141237.
Thompson E, Baraitser M (1987). "FG syndrome". J Med Genet. 24 (3): 139–43. doi:10.1136/jmg.24.3.139. PMC 1049945. PMID 3572995.
Opitz JM, Smith JF, Santoro L (2008). "The FG syndromes (Online Mendelian Inheritance in Man 305450): perspective in 2008". Adv Pediatr. 55: 123–70. doi:10.1016/j.yapd.2008.07.014. PMID 19048730.

"Faq Pages". FG Syndrome Family Alliance. fgsyndrome.org. Archived from the original on 26 February 2019. Retrieved 20 September 2016.

Opitz JM, Kaveggia EG (1974). "Studies of malformation syndromes of man XXXIII: the FG syndrome. An X-linked recessive syndrome of multiple congenital anomalies and mental retardation". Z Kinderheilkd. 117 (1): 1–18. doi:10.1007/BF00439020. PMID 4365204. S2CID 25141237.
Thompson E, Baraitser M (1987). "FG syndrome". J Med Genet. 24 (3): 139–43. doi:10.1136/jmg.24.3.139. PMC 1049945. PMID 3572995.
Lyons, M (1993). "MED12-Related Disorders". GeneReviews. University of Washington, Seattle. PMID 20301719. Retrieved 6 September 2016.
Lyons, Michael J. (1993), Adam, Margaret P.; Ardinger, Holly H.; Pagon, Roberta A.; Wallace, Stephanie E. (eds.), "MED12-Related Disorders", GeneReviews, Seattle (WA): University of Washington, Seattle, PMID 20301719, retrieved 2020-09-01
Opitz JM, Smith JF, Santoro L (2008). "The FG syndromes (Online Mendelian Inheritance in Man 305450): perspective in 2008". Adv Pediatr. 55: 123–70. doi:10.1016/j.yapd.2008.07.014. PMID 19048730.

Thompson E, Baraitser M (1987). "FG syndrome". J Med Genet. 24 (3): 139–43. doi:10.1136/jmg.24.3.139. PMC 1049945. PMID 3572995.
Lyons, M (1993). "MED12-Related Disorders". GeneReviews. University of Washington, Seattle. PMID 20301719. Retrieved 6 September 2016.
Lyons, Michael J. (1993), Adam, Margaret P.; Ardinger, Holly H.; Pagon, Roberta A.; Wallace, Stephanie E. (eds.), "MED12-Related Disorders", GeneReviews, Seattle (WA): University of Washington, Seattle, PMID 20301719, retrieved 2020-09-01

"MED12 - Genetics Home Reference". U.S. National Library of Medicine. Retrieved 6 September 2016.

Opitz JM, Kaveggia EG (1974). "Studies of malformation syndromes of man XXXIII: the FG syndrome. An X-linked recessive syndrome of multiple congenital anomalies and mental retardation". Z Kinderheilkd. 117 (1): 1–18. doi:10.1007/BF00439020. PMID 4365204. S2CID 25141237.

"Faq Pages". FG Syndrome Family Alliance. fgsyndrome.org. Archived from the original on 26 February 2019. Retrieved 20 September 2016.