Robinson HB - Search Results

1

Fetal age: methods of estimation and effects of pathology.

Sherwood RJ, Meindl RS, Robinson HB, May RL. Sherwood RJ, et al. Among authors: robinson hb. Am J Phys Anthropol. 2000 Nov;113(3):305-15. doi: 10.1002/1096-8644(200011)113:3<305::AID-AJPA3>3.0.CO;2-R. Am J Phys Anthropol. 2000. PMID: 11042534

2

Standardized residuals as a means for detection of growth alteration in the pathologic human fetus.

Sherwood RJ, Robinson HB, May RL, Meindl RS. Sherwood RJ, et al. Among authors: robinson hb. Teratology. 1992 Nov;46(5):419-27. doi: 10.1002/tera.1420460506. Teratology. 1992. PMID: 1462246

3

Pattern and process of growth of the abnormal human fetus.

Sherwood RJ, Robinson HB, Meindl RS, May RL. Sherwood RJ, et al. Among authors: robinson hb. Hum Biol. 1997 Dec;69(6):849-71. Hum Biol. 1997. PMID: 9353979

4

Exome sequencing identifies a novel EP300 frame shift mutation in a patient with features that overlap Cornelia de Lange syndrome.

Woods SA, Robinson HB, Kohler LJ, Agamanolis D, Sterbenz G, Khalifa M. Woods SA, et al. Among authors: robinson hb. Am J Med Genet A. 2014 Jan;164A(1):251-8. doi: 10.1002/ajmg.a.36237. Epub 2013 Oct 29. Am J Med Genet A. 2014. PMID: 24352918 Review.

5

A spectrum of phenotypical expression OF Neu-Laxova syndrome: Three case reports and a review of the literature.

Coto-Puckett WL, Gilbert-Barness E, Steelman CK, Stuart T, Robinson HB, Shehata BM. Coto-Puckett WL, et al. Among authors: robinson hb. Fetal Pediatr Pathol. 2010 Jan;29(2):108-19. doi: 10.3109/15513811003620914. Fetal Pediatr Pathol. 2010. PMID: 20334486

6

Genomic duplication resulting in increased copy number of genes encoding the sister chromatid cohesion complex conveys clinical consequences distinct from Cornelia de Lange.

Yan J, Zhang F, Brundage E, Scheuerle A, Lanpher B, Erickson RP, Powis Z, Robinson HB, Trapane PL, Stachiw-Hietpas D, Keppler-Noreuil KM, Lalani SR, Sahoo T, Chinault AC, Patel A, Cheung SW, Lupski JR. Yan J, et al. Among authors: robinson hb. J Med Genet. 2009 Sep;46(9):626-34. doi: 10.1136/jmg.2008.062471. Epub 2008 Dec 3. J Med Genet. 2009. PMID: 19052029 Free PMC article.

7

Prenatal echocardiographic diagnosis of a right aortic arch and bilateral arterial duct with isolation of the left subclavian artery from the left pulmonary artery.

Patel CR, Smith GL, Lane JR, Robinson HB. Patel CR, et al. Among authors: robinson hb. J Ultrasound Med. 2007 Aug;26(8):1107-10. doi: 10.7863/jum.2007.26.8.1107. J Ultrasound Med. 2007. PMID: 17646375 No abstract available.

8

Prenatal diagnosis of partial anomalous pulmonary venous connection in a patient with Fryns syndrome.

Patel CR, Smith GL, Robinson HB. Patel CR, et al. Among authors: robinson hb. J Ultrasound Med. 2007 Mar;26(3):403-6. doi: 10.7863/jum.2007.26.3.403. J Ultrasound Med. 2007. PMID: 17324994 No abstract available.

9

The feasibility of using histologic placental sections to predict newborn nucleated red blood cell counts.

Curtin WM, Shehata BM, Khuder SA, Robinson HB, Brost BC. Curtin WM, et al. Among authors: robinson hb. Obstet Gynecol. 2002 Aug;100(2):305-10. doi: 10.1016/s0029-7844(02)02041-0. Obstet Gynecol. 2002. PMID: 12151154

10

Weaver syndrome with neuroblastoma and cardiovascular anomalies.

Huffman C, McCandless D, Jasty R, Matloub J, Robinson HB, Weaver DD, Cohen MM Jr. Huffman C, et al. Among authors: robinson hb. Am J Med Genet. 2001 Mar 15;99(3):252-5. doi: 10.1002/1096-8628(2001)9999:9999<::aid-ajmg1169>3.0.co;2-l. Am J Med Genet. 2001. PMID: 11241499

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