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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2006 | 1 |
2007 | 5 |
2024 | 0 |
Search Results
6 results
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Page 1
A novel multiple congenital anomaly-mental retardation syndrome with Pierre Robin sequence and cerebellar hypoplasia in two sisters.
Am J Med Genet A. 2007 Oct 1;143A(19):2221-6. doi: 10.1002/ajmg.a.31945.
Am J Med Genet A. 2007.
PMID: 17764080
Free PMC article.
Gastric rupture and necrosis in Prader-Willi syndrome.
Stevenson DA, Heinemann J, Angulo M, Butler MG, Loker J, Rupe N, Kendell P, Cassidy SB, Scheimann A.
Stevenson DA, et al.
J Pediatr Gastroenterol Nutr. 2007 Aug;45(2):272-4. doi: 10.1097/MPG.0b013e31805b82b5.
J Pediatr Gastroenterol Nutr. 2007.
PMID: 17667731
Free PMC article.
Item in Clipboard
The use of anterolateral bowing of the lower leg in the diagnostic criteria for neurofibromatosis type 1.
Stevenson DA, Viskochil DH, Schorry EK, Crawford AH, D'Astous J, Murray KA, Friedman JM, Armstrong L, Carey JC.
Stevenson DA, et al.
Genet Med. 2007 Jul;9(7):409-12. doi: 10.1097/gim.0b013e3180986e05.
Genet Med. 2007.
PMID: 17666887
Free PMC article.
Review.
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Mandibulofacial dysostosis in a patient with a de novo 2;17 translocation that disrupts the HOXD gene cluster.
Stevenson DA, Bleyl SB, Maxwell T, Brothman AR, South ST.
Stevenson DA, et al.
Am J Med Genet A. 2007 May 15;143A(10):1053-9. doi: 10.1002/ajmg.a.31715.
Am J Med Genet A. 2007.
PMID: 17431905
Free PMC article.
Item in Clipboard
Deaths due to choking in Prader-Willi syndrome.
Stevenson DA, Heinemann J, Angulo M, Butler MG, Loker J, Rupe N, Kendell P, Clericuzio CL, Scheimann AO.
Stevenson DA, et al.
Am J Med Genet A. 2007 Mar 1;143A(5):484-7. doi: 10.1002/ajmg.a.31502.
Am J Med Genet A. 2007.
PMID: 17036318
Free PMC article.
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Clinical and molecular aspects of an informative family with neurofibromatosis type 1 and Noonan phenotype.
Stevenson DA, Viskochil DH, Rope AF, Carey JC.
Stevenson DA, et al.
Clin Genet. 2006 Mar;69(3):246-53. doi: 10.1111/j.1399-0004.2006.00576.x.
Clin Genet. 2006.
PMID: 16542390
Free PMC article.
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