Lamb AN - Search Results

1

Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome.

Estabrooks LL, Lamb AN, Aylsworth AS, Callanan NP, Rao KW. Estabrooks LL, et al. Among authors: lamb an. J Med Genet. 1994 Feb;31(2):103-7. doi: 10.1136/jmg.31.2.103. J Med Genet. 1994. PMID: 8182713 Free PMC article.

2

A molecular deletion of distal chromosome 4p in two families with a satellited chromosome 4 lacking the Wolf-Hirschhorn syndrome phenotype.

Estabrooks LL, Lamb AN, Kirkman HN, Callanan NP, Rao KW. Estabrooks LL, et al. Among authors: lamb an. Am J Hum Genet. 1992 Nov;51(5):971-8. Am J Hum Genet. 1992. PMID: 1384329 Free PMC article.

3

Familial 5p- syndrome.

Kushnick T, Rao KW, Lamb AN. Kushnick T, et al. Among authors: lamb an. Clin Genet. 1984 Nov;26(5):472-6. doi: 10.1111/j.1399-0004.1984.tb01091.x. Clin Genet. 1984. PMID: 6499259

4

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

5

American College of Medical Genetics recommendations for the design and performance expectations for clinical genomic copy number microarrays intended for use in the postnatal setting for detection of constitutional abnormalities.

Kearney HM, South ST, Wolff DJ, Lamb A, Hamosh A, Rao KW; Working Group of the American College of Medical Genetics. Kearney HM, et al. Genet Med. 2011 Jul;13(7):676-9. doi: 10.1097/GIM.0b013e31822272ac. Genet Med. 2011. PMID: 21681105 Free article.

6

Genotype-phenotype correlation in interstitial 6q deletions: a report of 12 new cases.

Rosenfeld JA, Amrom D, Andermann E, Andermann F, Veilleux M, Curry C, Fisher J, Deputy S, Aylsworth AS, Powell CM, Manickam K, Heese B, Maisenbacher M, Stevens C, Ellison JW, Upton S, Moeschler J, Torres-Martinez W, Stevens A, Marion R, Pereira EM, Babcock M, Morrow B, Sahoo T, Lamb AN, Ballif BC, Paciorkowski AR, Shaffer LG. Rosenfeld JA, et al. Among authors: lamb an. Neurogenetics. 2012 Feb;13(1):31-47. doi: 10.1007/s10048-011-0306-5. Epub 2012 Jan 5. Neurogenetics. 2012. PMID: 22218741

7

Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes.

Rosenfeld JA, Traylor RN, Schaefer GB, McPherson EW, Ballif BC, Klopocki E, Mundlos S, Shaffer LG, Aylsworth AS; 1q21.1 Study Group. Rosenfeld JA, et al. Eur J Hum Genet. 2012 Jul;20(7):754-61. doi: 10.1038/ejhg.2012.6. Epub 2012 Feb 8. Eur J Hum Genet. 2012. PMID: 22317977 Free PMC article.

8

Further clinical and molecular delineation of the 15q24 microdeletion syndrome.

Mefford HC, Rosenfeld JA, Shur N, Slavotinek AM, Cox VA, Hennekam RC, Firth HV, Willatt L, Wheeler P, Morrow EM, Cook J, Sullivan R, Oh A, McDonald MT, Zonana J, Keller K, Hannibal MC, Ball S, Kussmann J, Gorski J, Zelewski S, Banks V, Smith W, Smith R, Paull L, Rosenbaum KN, Amor DJ, Silva J, Lamb A, Eichler EE. Mefford HC, et al. J Med Genet. 2012 Feb;49(2):110-8. doi: 10.1136/jmedgenet-2011-100499. Epub 2011 Dec 17. J Med Genet. 2012. PMID: 22180641 Free PMC article.

9

Overwhelming maternal cell contamination in amniotic fluid samples from patients with oligohydramnios can lead to false prenatal interphase FISH results.

Estabrooks LL, Hanna JS, Lamb AN. Estabrooks LL, et al. Among authors: lamb an. Prenat Diagn. 1999 Feb;19(2):179-81. doi: 10.1002/(sici)1097-0223(199902)19:2<179::aid-pd473>3.0.co;2-1. Prenat Diagn. 1999. PMID: 10215080 No abstract available.

10

Ring 22 duplication/deletion mosaicism: clinical, cytogenetic, and molecular characterisation.

Frizzley JK, Stephan MJ, Lamb AN, Jonas PP, Hinson RM, Moffitt DR, Shkolny DL, McDermid HE. Frizzley JK, et al. Among authors: lamb an. J Med Genet. 1999 Mar;36(3):237-41. J Med Genet. 1999. PMID: 10204853 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

59 results

Search Page

Filters