PubMed (OMIM) for id: 376107

Year	Number of Results
1990	1
1996	1
1999	2
2002	1
2003	1
2004	1
2005	1
2023	0

1

Genetics of the polymicrogyria syndromes.

Jansen A, Andermann E. Jansen A, et al. J Med Genet. 2005 May;42(5):369-78. doi: 10.1136/jmg.2004.023952. J Med Genet. 2005. PMID: 15863665 Free PMC article. Review.

2

G protein-coupled receptor-dependent development of human frontal cortex.

Piao X, Hill RS, Bodell A, Chang BS, Basel-Vanagaite L, Straussberg R, Dobyns WB, Qasrawi B, Winter RM, Innes AM, Voit T, Ross ME, Michaud JL, Déscarie JC, Barkovich AJ, Walsh CA. Piao X, et al. Science. 2004 Mar 26;303(5666):2033-6. doi: 10.1126/science.1092780. Science. 2004. PMID: 15044805

3

Bilateral frontoparietal polymicrogyria: clinical and radiological features in 10 families with linkage to chromosome 16.

Chang BS, Piao X, Bodell A, Basel-Vanagaite L, Straussberg R, Dobyns WB, Qasrawi B, Winter RM, Innes AM, Voit T, Grant PE, Barkovich AJ, Walsh CA. Chang BS, et al. Ann Neurol. 2003 May;53(5):596-606. doi: 10.1002/ana.10520. Ann Neurol. 2003. PMID: 12730993

4

An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21.

Piao X, Basel-Vanagaite L, Straussberg R, Grant PE, Pugh EW, Doheny K, Doan B, Hong SE, Shugart YY, Walsh CA. Piao X, et al. Am J Hum Genet. 2002 Apr;70(4):1028-33. doi: 10.1086/339552. Epub 2002 Feb 13. Am J Hum Genet. 2002. PMID: 11845408 Free PMC article.

5

TM7XN1, a novel human EGF-TM7-like cDNA, detected with mRNA differential display using human melanoma cell lines with different metastatic potential.

Zendman AJ, Cornelissen IM, Weidle UH, Ruiter DJ, van Muijen GN. Zendman AJ, et al. FEBS Lett. 1999 Mar 12;446(2-3):292-8. doi: 10.1016/s0014-5793(99)00230-6. FEBS Lett. 1999. PMID: 10100861 Free article.

6

GPR56, a novel secretin-like human G-protein-coupled receptor gene.

Liu M, Parker RM, Darby K, Eyre HJ, Copeland NG, Crawford J, Gilbert DJ, Sutherland GR, Jenkins NA, Herzog H. Liu M, et al. Genomics. 1999 Feb 1;55(3):296-305. doi: 10.1006/geno.1998.5644. Genomics. 1999. PMID: 10049584

7

A new autosomal recessive syndrome of pachygyria.

Straussberg R, Gross S, Amir J, Gadoth N. Straussberg R, et al. Clin Genet. 1996 Dec;50(6):498-501. doi: 10.1111/j.1399-0004.1996.tb02721.x. Clin Genet. 1996. PMID: 9147882

8

Ataxia, developmental delay and an extensive neuronal migration abnormality in 2 siblings.

Harbord MG, Boyd S, Hall-Craggs MA, Kendall B, McShane MA, Baraitser M. Harbord MG, et al. Neuropediatrics. 1990 Nov;21(4):218-21. doi: 10.1055/s-2008-1071501. Neuropediatrics. 1990. PMID: 2290486

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