Continuing Education Opportunities.
- Published in:
- Journal of the Association of Genetic Technologists, 2017, v. 43, n. 3, p. 136
- By:
- Publication type:
- Article
Works by Kochmar, Sally J.
Results: 11
1
2
Continuing Education Opportunities.
- Published in:
- 2017
- By:
- Publication type:
- Test/Instrument
3
Test Yourself #4, 2016.
- Published in:
- Journal of the Association of Genetic Technologists, 2016, v. 42, n. 4, p. 193
- By:
- Publication type:
- Article
4
Test Yourself #2, 2016.
- Published in:
- 2016
- By:
- Publication type:
- Test/Instrument
5
Test Yourself #2, 2014.
- Published in:
- Journal of the Association of Genetic Technologists, 2014, v. 40, n. 2, p. 99
- By:
- Publication type:
- Article
6
Seizure Disorder in a Patient with a 5.09 Mb 7q11.23-q21.11 Microdeletion Including the MAGI2 Gene.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
7
Test Yourself #3, 2013.
- Published in:
- Journal of the Association of Genetic Technologists, 2013, v. 39, n. 3, p. 115
- By:
- Publication type:
- Article
8
Prenatal Diagnosis of 2q32 Deletion Syndrome Characterized by Multiple Segmental Deletions and Complex Chromosomal Rearrangement Involving Chromosomes 2, 5 and 7.
- Published in:
- Fetal Diagnosis & Therapy, 2012, v. 31, n. 3, p. 196, doi. 10.1159/000335650
- By:
- Publication type:
- Article
9
Prenatal detection of del(10)(q11.2) mosaicism in chorionic villus specimens likely caused by a common chromosomal fragile site FRA10G is associated with a normal phenotype.
- Published in:
- Prenatal Diagnosis, 2012, v. 32, n. 12, p. 1166, doi. 10.1002/pd.3977
- By:
- Publication type:
- Article
10
The use of interphase FISH for prenatal diagnosis of Pallister-Killian syndrome.
- Published in:
- 1997
- By:
- Publication type:
- journal article
11
Chromosome 12q13.13q13.13 microduplication and microdeletion: a case report and literature review.
- Published in:
- 2017
- By:
- Publication type:
- Case Study