Ledbetter DH - Search Results

1

Clinical outcomes of a genomic screening program for actionable genetic conditions.

Buchanan AH, Lester Kirchner H, Schwartz MLB, Kelly MA, Schmidlen T, Jones LK, Hallquist MLG, Rocha H, Betts M, Schwiter R, Butry L, Lazzeri AL, Frisbie LR, Rahm AK, Hao J, Willard HF, Martin CL, Ledbetter DH, Williams MS, Sturm AC. Buchanan AH, et al. Among authors: ledbetter dh. Genet Med. 2020 Nov;22(11):1874-1882. doi: 10.1038/s41436-020-0876-4. Epub 2020 Jun 30. Genet Med. 2020. PMID: 32601386 Free PMC article.

2

Five polymorphic microsatellite VNTRs on the human X chromosome.

Luty JA, Guo Z, Willard HF, Ledbetter DH, Ledbetter S, Litt M. Luty JA, et al. Among authors: ledbetter s, ledbetter dh. Am J Hum Genet. 1990 Apr;46(4):776-83. Am J Hum Genet. 1990. PMID: 2316523 Free PMC article.

3

Autism and cytogenetic abnormalities: solving autism one chromosome at a time.

Martin CL, Ledbetter DH. Martin CL, et al. Among authors: ledbetter dh. Curr Psychiatry Rep. 2007 Apr;9(2):141-7. doi: 10.1007/s11920-007-0084-9. Curr Psychiatry Rep. 2007. PMID: 17389126 Review.

4

The evolution of molecular ruler analysis for characterizing telomere imbalances: from fluorescence in situ hybridization to array comparative genomic hybridization.

Martin CL, Nawaz Z, Baldwin EL, Wallace EJ, Justice AN, Ledbetter DH. Martin CL, et al. Among authors: ledbetter dh. Genet Med. 2007 Sep;9(9):566-73. doi: 10.1097/gim.0b013e318149e1fc. Genet Med. 2007. PMID: 17873644 Free article. Review.

5

Cryptic telomere imbalance: a 15-year update.

Ledbetter DH, Martin CL. Ledbetter DH, et al. Am J Med Genet C Semin Med Genet. 2007 Nov 15;145C(4):327-34. doi: 10.1002/ajmg.c.30149. Am J Med Genet C Semin Med Genet. 2007. PMID: 17910073 Review.

6

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene.

Alarcón M, Abrahams BS, Stone JL, Duvall JA, Perederiy JV, Bomar JM, Sebat J, Wigler M, Martin CL, Ledbetter DH, Nelson SF, Cantor RM, Geschwind DH. Alarcón M, et al. Among authors: ledbetter dh. Am J Hum Genet. 2008 Jan;82(1):150-9. doi: 10.1016/j.ajhg.2007.09.005. Am J Hum Genet. 2008. PMID: 18179893 Free PMC article.

7

Mechanisms and consequences of small supernumerary marker chromosomes: from Barbara McClintock to modern genetic-counseling issues.

Baldwin EL, May LF, Justice AN, Martin CL, Ledbetter DH. Baldwin EL, et al. Among authors: ledbetter dh. Am J Hum Genet. 2008 Feb;82(2):398-410. doi: 10.1016/j.ajhg.2007.10.013. Am J Hum Genet. 2008. PMID: 18252220 Free PMC article.

8

Enhanced detection of clinically relevant genomic imbalances using a targeted plus whole genome oligonucleotide microarray.

Baldwin EL, Lee JY, Blake DM, Bunke BP, Alexander CR, Kogan AL, Ledbetter DH, Martin CL. Baldwin EL, et al. Among authors: ledbetter dh. Genet Med. 2008 Jun;10(6):415-29. doi: 10.1097/GIM.0b013e318177015c. Genet Med. 2008. PMID: 18496225 Free article.

9

Adaptor protein complex-4 (AP-4) deficiency causes a novel autosomal recessive cerebral palsy syndrome with microcephaly and intellectual disability.

Moreno-De-Luca A, Helmers SL, Mao H, Burns TG, Melton AM, Schmidt KR, Fernhoff PM, Ledbetter DH, Martin CL. Moreno-De-Luca A, et al. Among authors: ledbetter dh. J Med Genet. 2011 Feb;48(2):141-4. doi: 10.1136/jmg.2010.082263. Epub 2010 Oct 23. J Med Genet. 2011. PMID: 20972249 Free PMC article.

10

Genetic [corrected] insights into the causes and classification of [corrected] cerebral palsies.

Moreno-De-Luca A, Ledbetter DH, Martin CL. Moreno-De-Luca A, et al. Among authors: ledbetter dh. Lancet Neurol. 2012 Mar;11(3):283-92. doi: 10.1016/S1474-4422(11)70287-3. Epub 2012 Jan 18. Lancet Neurol. 2012. PMID: 22261432 Free PMC article. Review.

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