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Items: 4


Genomic and epigenetic evidence for oxytocin receptor deficiency in autism.

Gregory SG, Connelly JJ, Towers AJ, Johnson J, Biscocho D, Markunas CA, Lintas C, Abramson RK, Wright HH, Ellis P, Langford CF, Worley G, Delong GR, Murphy SK, Cuccaro ML, Persico A, Pericak-Vance MA.

BMC Med. 2009 Oct 22;7:62. doi: 10.1186/1741-7015-7-62.


Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism.

Ma DQ, Whitehead PL, Menold MM, Martin ER, Ashley-Koch AE, Mei H, Ritchie MD, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Hussman JP, Gilbert JR, Pericak-Vance MA.

Am J Hum Genet. 2005 Sep;77(3):377-88. Epub 2005 Jul 15.


Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes.

Shao Y, Cuccaro ML, Hauser ER, Raiford KL, Menold MM, Wolpert CM, Ravan SA, Elston L, Decena K, Donnelly SL, Abramson RK, Wright HH, DeLong GR, Gilbert JR, Pericak-Vance MA.

Am J Hum Genet. 2003 Mar;72(3):539-48. Epub 2003 Feb 3.


Sylvian aqueduct syndrome as a sign of acute obstructive hydrocephalus in children.

Chattha AS, Delong GR.

J Neurol Neurosurg Psychiatry. 1975 Mar;38(3):288-96.

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