Meck JM - Search Results

Year	Number of Results
1975	1
1979	1
1980	1
1981	2
1982	1
1983	1
1984	2
1986	1
1990	1
1991	1
1992	1
1993	1
1994	3
1995	1
1996	2
1999	4
2000	2
2001	1
2002	1
2004	1
2005	1
2006	2
2007	3
2008	2
2009	3
2010	5
2015	2
2017	1
2019	1
2020	2
2025	0

1

Adapting ACMG/AMP sequence variant classification guidelines for single-gene copy number variants.

Brandt T, Sack LM, Arjona D, Tan D, Mei H, Cui H, Gao H, Bean LJH, Ankala A, Del Gaudio D, Knight Johnson A, Vincent LM, Reavey C, Lai A, Richard G, Meck JM. Brandt T, et al. Among authors: meck jm. Genet Med. 2020 Feb;22(2):336-344. doi: 10.1038/s41436-019-0655-2. Epub 2019 Sep 19. Genet Med. 2020. PMID: 31534211 Free article.

2

Holoprosencephaly due to numeric chromosome abnormalities.

Solomon BD, Rosenbaum KN, Meck JM, Muenke M. Solomon BD, et al. Among authors: meck jm. Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):146-8. doi: 10.1002/ajmg.c.30232. Am J Med Genet C Semin Med Genet. 2010. PMID: 20104610 Free PMC article. Review.

3

Familial 10p trisomy resulting from a maternal pericentric inversion.

Kozma C, Meck JM. Kozma C, et al. Among authors: meck jm. Am J Med Genet. 1994 Feb 1;49(3):281-7. doi: 10.1002/ajmg.1320490308. Am J Med Genet. 1994. PMID: 8209887 Review.

4

Reply: To PMID 25843063.

Meck JM, Cherry AM. Meck JM, et al. Am J Obstet Gynecol. 2015 Oct;213(4):596. doi: 10.1016/j.ajog.2015.06.007. Epub 2015 Jun 9. Am J Obstet Gynecol. 2015. PMID: 26070704 No abstract available.

5

Cytogenetic abnormalities in attention-deficit/hyperactivity disorder.

Bastain TM, Lewczyk CM, Sharp WS, James RS, Long RT, Eagen PB, Ebens CL, Meck JM, Chan WY, Sidransky E, Rapoport JL, Castellanos FX. Bastain TM, et al. Among authors: meck jm. J Am Acad Child Adolesc Psychiatry. 2002 Jul;41(7):806-10. doi: 10.1097/00004583-200207000-00012. J Am Acad Child Adolesc Psychiatry. 2002. PMID: 12108805

6

Correction: Adapting ACMG/AMP sequence variant classification guidelines for single-gene copy-number variants.

Brandt T, Sack LM, Arjona D, Tan D, Mei H, Cui H, Gao H, Bean LJH, Ankala A, Del Gaudio D, Johnson AK, Vincent LM, Reavey C, Lai A, Richard G, Meck JM. Brandt T, et al. Among authors: meck jm. Genet Med. 2020 Mar;22(3):670-671. doi: 10.1038/s41436-019-0725-5. Genet Med. 2020. PMID: 31844178 Free article.

7

Prenatal diagnosis of supernumerary ring chromosome 1: case report and review of the literature.

Wray AM, Dennis TR, Ghidini A, Gorman B, Haddad BR, Meck JM. Wray AM, et al. Among authors: meck jm. Genet Couns. 2007;18(2):233-41. Genet Couns. 2007. PMID: 17710876 Review.

8

Noninvasive prenatal screening for aneuploidy: positive predictive values based on cytogenetic findings.

Meck JM, Kramer Dugan E, Matyakhina L, Aviram A, Trunca C, Pineda-Alvarez D, Aradhya S, Klein RT, Cherry AM. Meck JM, et al. Am J Obstet Gynecol. 2015 Aug;213(2):214.e1-5. doi: 10.1016/j.ajog.2015.04.001. Epub 2015 Apr 3. Am J Obstet Gynecol. 2015. PMID: 25843063

9

Factor VII deficiency and developmental abnormalities in a patient with partial monosomy of 13q and trisomy of 16p: case report and review of the literature.

Brooks BP, Meck JM, Haddad BR, Bendavid C, Blain D, Toretsky JA. Brooks BP, et al. Among authors: meck jm. BMC Med Genet. 2006 Jan 13;7:2. doi: 10.1186/1471-2350-7-2. BMC Med Genet. 2006. PMID: 16412230 Free PMC article. Review.

10

Deletion 6p as the sole chromosome abnormality in a patient with therapy-related myelodysplastic syndrome: case report and review of the literature.

Meloni-Ehrig AM, Alexander E, Nathan SV, Ahmed MS, Smith ED, Scheerle JA, Kelly JC, Meck JM, Mowrey PN. Meloni-Ehrig AM, et al. Among authors: meck jm. Cancer Genet Cytogenet. 2010 Feb;197(1):81-3. doi: 10.1016/j.cancergencyto.2009.11.002. Cancer Genet Cytogenet. 2010. PMID: 20113842 Review. No abstract available.

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