Shanske AL - Search Results

1

Letter to the editor: Hidden pituitary gland: implications for assessment.

Paroder V, Miller T, Shanske AL, Shiota K, Khan MN, Cohen MM Jr. Paroder V, et al. Among authors: shanske al. Am J Med Genet A. 2013 Mar;161A(3):630-1. doi: 10.1002/ajmg.a.35880. Epub 2013 Feb 7. Am J Med Genet A. 2013. PMID: 23401199 No abstract available.

2

Absent sella turcica: a case report and a review of the literature.

Paroder V, Miller T, Cohen MM Jr, Shanske AL. Paroder V, et al. Among authors: shanske al. Fetal Pediatr Pathol. 2013 Oct;32(5):375-83. doi: 10.3109/15513815.2013.799249. Epub 2013 May 20. Fetal Pediatr Pathol. 2013. PMID: 23688421 Review.

3

Interparietal bone (Os Incae) in craniosynostosis.

Wu JK, Goodrich JT, Amadi CC, Miller T, Mulliken JB, Shanske AL. Wu JK, et al. Among authors: shanske al. Am J Med Genet A. 2011 Feb;155A(2):287-94. doi: 10.1002/ajmg.a.33800. Epub 2010 Dec 22. Am J Med Genet A. 2011. PMID: 21271643 Review.

4

Trisomy 18 in a second 20-year-old woman.

Shanske AL. Shanske AL. Am J Med Genet A. 2006 May 1;140(9):966-7. doi: 10.1002/ajmg.a.31171. Am J Med Genet A. 2006. PMID: 16575893 No abstract available.

5

A syndrome of holoprosencephaly, recurrent infections, and monocytosis.

Jubinsky PT, Shanske AL, Pixley FJ, Montagna C, Short MK. Jubinsky PT, et al. Among authors: shanske al. Am J Med Genet A. 2006 Dec 15;140(24):2742-8. doi: 10.1002/ajmg.a.31542. Am J Med Genet A. 2006. PMID: 17103456

6

Detection of an interstitial deletion of 2q21-22 by high resolution comparative genomic hybridization in a child with multiple congenital anomalies and an apparent balanced translocation.

Shanske AL, Edelmann L, Kardon NB, Gosset P, Levy B. Shanske AL, et al. Am J Med Genet A. 2004 Nov 15;131(1):29-35. doi: 10.1002/ajmg.a.30311. Am J Med Genet A. 2004. PMID: 15368480 Review.

7

The proximal chromosome 14q microdeletion syndrome: delineation of the phenotype using high resolution SNP oligonucleotide microarray analysis (SOMA) and review of the literature.

Torgyekes E, Shanske AL, Anyane-Yeboa K, Nahum O, Pirzadeh S, Blumfield E, Jobanputra V, Warburton D, Levy B. Torgyekes E, et al. Among authors: shanske al. Am J Med Genet A. 2011 Aug;155A(8):1884-96. doi: 10.1002/ajmg.a.34090. Epub 2011 Jul 8. Am J Med Genet A. 2011. PMID: 21744488 Review.

8

Chorea associated with antiphospholipid antibodies in a patient with Kabuki syndrome.

Gidwani P, Segal E, Shanske A, Driscoll C. Gidwani P, et al. Am J Med Genet A. 2007 Jun 15;143A(12):1338-41. doi: 10.1002/ajmg.a.31774. Am J Med Genet A. 2007. PMID: 17506095

9

Central nervous system anomalies in Seckel syndrome: report of a new family and review of the literature.

Shanske A, Marion R. Shanske A, et al. Am J Med Genet. 1998 May 18;77(3):250. Am J Med Genet. 1998. PMID: 9605595 No abstract available.

10

The Marshall syndrome: report of a new family and review of the literature.

Shanske AL, Bogdanow A, Shprintzen RJ, Marion RW. Shanske AL, et al. Am J Med Genet. 1997 May 2;70(1):52-7. doi: 10.1002/(sici)1096-8628(19970502)70:1<52::aid-ajmg11>3.0.co;2-w. Am J Med Genet. 1997. PMID: 9129742 Review.

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