Detalhe da pesquisa
1.
Adapting ACMG/AMP sequence variant classification guidelines for single-gene copy number variants.
Genet Med
; 22(2): 336-344, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31534211
2.
Correction: Adapting ACMG/AMP sequence variant classification guidelines for single-gene copy-number variants.
Genet Med
; 22(3): 670-671, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-31844178
3.
Diagnostic cytogenetic testing following positive noninvasive prenatal screening results: a clinical laboratory practice resource of the American College of Medical Genetics and Genomics (ACMG).
Genet Med
; 19(8): 845-850, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28726804
4.
Noninvasive prenatal screening for aneuploidy: positive predictive values based on cytogenetic findings.
Am J Obstet Gynecol
; 213(2): 214.e1-5, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25843063
5.
Cooperation of tumor-derived HBx mutants and p53-249(ser) mutant in regulating cell proliferation, anchorage-independent growth and aneuploidy in a telomerase-immortalized normal human hepatocyte-derived cell line.
Int J Cancer
; 127(5): 1011-20, 2010 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20017137
6.
Holoprosencephaly due to numeric chromosome abnormalities.
Am J Med Genet C Semin Med Genet
; 154C(1): 146-8, 2010 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20104610
7.
Reply: To PMID 25843063.
Am J Obstet Gynecol
; 213(4): 596, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26070704
8.
Statement on guidance for genetic counseling in advanced paternal age.
Genet Med
; 10(6): 457-60, 2008 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-18496227
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.
BMC Med Genet
; 7: 2, 2006 Jan 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-16412230
10.
Molecular cytogenetic characterization of two small supernumerary marker chromosomes derived from chromosome 19.
Am J Med Genet A
; 149A(2): 262-5, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19133694
11.
Cytogenetic abnormalities in attention-deficit/hyperactivity disorder.
J Am Acad Child Adolesc Psychiatry
; 41(7): 806-10, 2002 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-12108805
12.
Long-term persistence of nonpathogenic clonal chromosome abnormalities in donor hematopoietic cells after allogeneic stem cell transplantation.
Cancer Genet Cytogenet
; 190(2): 125-30, 2009 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19380032
13.
MDA-MB-435 cells are derived from M14 melanoma cells--a loss for breast cancer, but a boon for melanoma research.
Breast Cancer Res Treat
; 104(1): 13-9, 2007 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-17004106
14.
Deletion 6p as the sole chromosome abnormality in a patient with therapy-related myelodysplastic syndrome: case report and review of the literature.
Cancer Genet Cytogenet
; 197(1): 81-3, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20113842
15.
Segregation of a t(1;3) translocation in multiple affected family members with both types of adjacent-1 segregants.
Am J Med Genet A
; 124A(2): 118-28, 2004 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-14699608
16.
A rare finding of deletion 5q in a child with juvenile myelomonocytic leukemia.
Cancer Genet Cytogenet
; 195(2): 192-4, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19963125