Beaulieu-Bergeron M - Search Results

1

A 79-kb paternally inherited 7q32.2 microdeletion involving MEST in a patient with a Silver-Russell syndrome-like phenotype.

Vincent KM, Stavropoulos DJ, Beaulieu-Bergeron M, Yang C, Jiang M, Zuijdwijk C, Dyment DA, Graham GE. Vincent KM, et al. Among authors: beaulieu bergeron m. Am J Med Genet A. 2022 Aug;188(8):2421-2428. doi: 10.1002/ajmg.a.62782. Epub 2022 May 20. Am J Med Genet A. 2022. PMID: 35593535

2

A splice site and copy number variant responsible for TTC25-related primary ciliary dyskinesia.

Backman K, Mears WE, Waheeb A, Beaulieu Bergeron M, McClintock J, de Nanassy J, Reisman J, Osmond M, Hartley T, Mears AJ, Kernohan KD; Care4Rare Canada. Backman K, et al. Among authors: beaulieu bergeron m. Eur J Med Genet. 2021 May;64(5):104193. doi: 10.1016/j.ejmg.2021.104193. Epub 2021 Mar 18. Eur J Med Genet. 2021. PMID: 33746037

3

Male pseudohermaphroditism and gonadal mosaicism in a 47,XY,+22 fetus.

Beaulieu Bergeron M, Tran-Thanh D, Fournet JC, Lemyre E, Lemieux N, Bouron-Dal Soglio D. Beaulieu Bergeron M, et al. Am J Med Genet A. 2006 Aug 15;140(16):1768-72. doi: 10.1002/ajmg.a.31338. Am J Med Genet A. 2006. PMID: 16835917

4

A rare case of acute leukemia of ambiguous lineage overexpressing C-MYC with monosomy 7 and Philadelphia chromosome.

Xu Z, Padmore R, Shier L, Beaulieu Bergeron M. Xu Z, et al. Among authors: beaulieu bergeron m. Ann Hematol. 2015 Oct;94(10):1761-3. doi: 10.1007/s00277-015-2443-7. Epub 2015 Jul 11. Ann Hematol. 2015. PMID: 26159563 No abstract available.

5

Correlation of intercentromeric distance, mosaicism, and sexual phenotype: molecular localization of breakpoints in isodicentric Y chromosomes.

Beaulieu Bergeron M, Brochu P, Lemyre E, Lemieux N. Beaulieu Bergeron M, et al. Am J Med Genet A. 2011 Nov;155A(11):2705-12. doi: 10.1002/ajmg.a.34260. Epub 2011 Sep 30. Am J Med Genet A. 2011. PMID: 21964771

6

ALU transposition induces familial hypertrophic cardiomyopathy.

Nfonsam L, Huang L, Carson N, McGowan-Jordan J, Beaulieu Bergeron M, Goobie S, Conacher S, McCarty D, Benson L, Hewson S, Zahavich L, Sinclair-Bourque E, Smith A, Potter R, Ghani M, Bronicki L, Jarinova O. Nfonsam L, et al. Among authors: beaulieu bergeron m. Mol Genet Genomic Med. 2020 Jan;8(1):e951. doi: 10.1002/mgg3.951. Epub 2019 Sep 30. Mol Genet Genomic Med. 2020. PMID: 31568709 Free PMC article.

7

Phenotypic variability in isodicentric Y patients: study of nine cases.

DesGroseilliers M, Beaulieu Bergeron M, Brochu P, Lemyre E, Lemieux N. DesGroseilliers M, et al. Clin Genet. 2006 Aug;70(2):145-50. doi: 10.1111/j.1399-0004.2006.00654.x. Clin Genet. 2006. PMID: 16879197

8

Undifferentiated gonadal tissue, Y chromosome instability, and tumors in XY gonadal dysgenesis.

Beaulieu Bergeron M, Lemieux N, Brochu P. Beaulieu Bergeron M, et al. Pediatr Dev Pathol. 2011 Nov-Dec;14(6):445-59. doi: 10.2350/11-01-0960-OA.1. Epub 2011 Jun 21. Pediatr Dev Pathol. 2011. PMID: 21692598

9

Identification of new susceptibility regions for X;Y translocations in patients with testicular disorder of sex development.

Beaulieu Bergeron M, Lemyre E, Lemieux N. Beaulieu Bergeron M, et al. Sex Dev. 2011;5(1):1-6. doi: 10.1159/000321995. Epub 2010 Nov 17. Sex Dev. 2011. PMID: 21088380

10

Coexistence of a choriocarcinoma and a gonadoblastoma in the gonad of a 46,XY female: a single nucleotide polymorphism array analysis.

Beaulieu Bergeron M, Soglio DB, Maietta A, Fournet JC, Blumenkrantz M, Brochu P, Lemieux N. Beaulieu Bergeron M, et al. Pediatr Dev Pathol. 2010 Jan-Feb;13(1):66-71. doi: 10.2350/09-02-0606-CR.1. Pediatr Dev Pathol. 2010. PMID: 19425818

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

16 results

Search Page

Filters