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Items: 7

1.

Subacute concussion-related symptoms and postconcussion syndrome in pediatrics.

Blume H, Hawash K.

Curr Opin Pediatr. 2012 Dec;24(6):724-30. doi: 10.1097/MOP.0b013e328359e4cc. Review.

PMID:
23128838
2.

Age- and gender-dependent obesity in individuals with 16p11.2 deletion.

Yu Y, Zhu H, Miller DT, Gusella JF, Platt OS, Wu BL, Shen Y; Children's Hospital Boston Genotype Phenotype Study Group.

J Genet Genomics. 2011 Sep 20;38(9):403-9. doi: 10.1016/j.jgg.2011.08.003. Epub 2011 Aug 17.

PMID:
21930099
3.

A recurrent 1.71 Mb genomic imbalance at 2q13 increases the risk of developmental delay and dysmorphism.

Yu HE, Hawash K, Picker J, Stoler J, Urion D, Wu BL, Shen Y.

Clin Genet. 2012 Mar;81(3):257-64. doi: 10.1111/j.1399-0004.2011.01637.x. Epub 2011 Feb 7.

PMID:
21255006
4.

Cognitive and behavioral characterization of 16p11.2 deletion syndrome.

Hanson E, Nasir RH, Fong A, Lian A, Hundley R, Shen Y, Wu BL, Holm IA, Miller DT; 16p11.2 Study Group Clinicians.

J Dev Behav Pediatr. 2010 Oct;31(8):649-57. doi: 10.1097/DBP.0b013e3181ea50ed.

PMID:
20613623
5.

Clinical genetic testing for patients with autism spectrum disorders.

Shen Y, Dies KA, Holm IA, Bridgemohan C, Sobeih MM, Caronna EB, Miller KJ, Frazier JA, Silverstein I, Picker J, Weissman L, Raffalli P, Jeste S, Demmer LA, Peters HK, Brewster SJ, Kowalczyk SJ, Rosen-Sheidley B, McGowan C, Duda AW 3rd, Lincoln SA, Lowe KR, Schonwald A, Robbins M, Hisama F, Wolff R, Becker R, Nasir R, Urion DK, Milunsky JM, Rappaport L, Gusella JF, Walsh CA, Wu BL, Miller DT; Autism Consortium Clinical Genetics/DNA Diagnostics Collaboration.

Pediatrics. 2010 Apr;125(4):e727-35. doi: 10.1542/peds.2009-1684. Epub 2010 Mar 15.

6.

Is Rolandic epilepsy associated with abnormal findings on cranial MRI?

Boxerman JL, Hawash K, Bali B, Clarke T, Rogg J, Pal DK.

Epilepsy Res. 2007 Jul;75(2-3):180-5.

7.

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