Lamb AN - Search Results

1

Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities.

Ravnan JB, Tepperberg JH, Papenhausen P, Lamb AN, Hedrick J, Eash D, Ledbetter DH, Martin CL. Ravnan JB, et al. Among authors: lamb an. J Med Genet. 2006 Jun;43(6):478-89. doi: 10.1136/jmg.2005.036350. Epub 2005 Sep 30. J Med Genet. 2006. PMID: 16199540 Free PMC article.

2

Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems.

Sahoo T, Theisen A, Rosenfeld JA, Lamb AN, Ravnan JB, Schultz RA, Torchia BS, Neill N, Casci I, Bejjani BA, Shaffer LG. Sahoo T, et al. Among authors: lamb an. Genet Med. 2011 Oct;13(10):868-80. doi: 10.1097/GIM.0b013e3182217a06. Genet Med. 2011. PMID: 21792059 Free article.

3

Identification of an unusual marker chromosome by spectral karyotyping.

Huang B, Ning Y, Lamb AN, Sandlin CJ, Jamehdor M, Ried T, Bartley J. Huang B, et al. Among authors: lamb an. Am J Med Genet. 1998 Dec 4;80(4):368-72. Am J Med Genet. 1998. PMID: 9856565

4

Clinical features associated with copy number variations of the 14q32 imprinted gene cluster.

Rosenfeld JA, Fox JE, Descartes M, Brewer F, Stroud T, Gorski JL, Upton SJ, Moeschler JB, Monteleone B, Neill NJ, Lamb AN, Ballif BC, Shaffer LG, Ravnan JB. Rosenfeld JA, et al. Among authors: lamb an. Am J Med Genet A. 2015 Feb;167A(2):345-53. doi: 10.1002/ajmg.a.36866. Am J Med Genet A. 2015. PMID: 25756153

5

Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders.

Rosenfeld JA, Ballif BC, Torchia BS, Sahoo T, Ravnan JB, Schultz R, Lamb A, Bejjani BA, Shaffer LG. Rosenfeld JA, et al. Genet Med. 2010 Nov;12(11):694-702. doi: 10.1097/GIM.0b013e3181f0c5f3. Genet Med. 2010. PMID: 20808228 Free article.

6

Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).

Waggoner D, Wain KE, Dubuc AM, Conlin L, Hickey SE, Lamb AN, Martin CL, Morton CC, Rasmussen K, Schuette JL, Schwartz S, Miller DT; ACMG Professional Practice and Guidelines Committee. Waggoner D, et al. Among authors: lamb an. Genet Med. 2018 Oct;20(10):1105-1113. doi: 10.1038/s41436-018-0040-6. Epub 2018 Jun 18. Genet Med. 2018. PMID: 29915380 Free PMC article. Review.

7

Recurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISH.

Neill NJ, Ballif BC, Lamb AN, Parikh S, Ravnan JB, Schultz RA, Torchia BS, Rosenfeld JA, Shaffer LG. Neill NJ, et al. Among authors: lamb an. Genome Res. 2011 Apr;21(4):535-44. doi: 10.1101/gr.114579.110. Epub 2011 Mar 7. Genome Res. 2011. PMID: 21383316 Free PMC article.

8

High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44.

Ballif BC, Rosenfeld JA, Traylor R, Theisen A, Bader PI, Ladda RL, Sell SL, Steinraths M, Surti U, McGuire M, Williams S, Farrell SA, Filiano J, Schnur RE, Coffey LB, Tervo RC, Stroud T, Marble M, Netzloff M, Hanson K, Aylsworth AS, Bamforth JS, Babu D, Niyazov DM, Ravnan JB, Schultz RA, Lamb AN, Torchia BS, Bejjani BA, Shaffer LG. Ballif BC, et al. Among authors: lamb an. Hum Genet. 2012 Jan;131(1):145-56. doi: 10.1007/s00439-011-1073-y. Epub 2011 Jul 29. Hum Genet. 2012. PMID: 21800092

9

Defining the impact of maternal cell contamination on the interpretation of prenatal microarray analysis.

Lamb AN, Rosenfeld JA, Coppinger J, Dodge ET, Dabell MP, Torchia BS, Ravnan JB, Shaffer LG, Ballif BC. Lamb AN, et al. Genet Med. 2012 Nov;14(11):914-21. doi: 10.1038/gim.2012.77. Epub 2012 Jul 5. Genet Med. 2012. PMID: 22766610 Free article.

10

Prenatal diagnosis from fetal urine in bladder outlet obstruction: success rates for traditional cytogenetic evaluation and interphase fluorescence in situ hybridization.

Donnenfeld AE, Lockwood D, Custer T, Lamb AN. Donnenfeld AE, et al. Among authors: lamb an. Genet Med. 2002 Nov-Dec;4(6):444-7. doi: 10.1097/00125817-200211000-00008. Genet Med. 2002. PMID: 12509716

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