Search details
1.
Graduate training, credentialing, and continuing education to prepare genetic counselors for laboratory roles-Results of a national survey.
J Genet Couns
; 2024 Feb 09.
Article
in English
| MEDLINE | ID: mdl-38339832
2.
Need for additional training to be a laboratory genetic counselor-A qualitative exploration.
J Genet Couns
; 32(6): 1249-1265, 2023 Dec.
Article
in English
| MEDLINE | ID: mdl-37493003
3.
Stankiewicz-Isidor syndrome: expanding the clinical and molecular phenotype.
Genet Med
; 24(1): 179-191, 2022 01.
Article
in English
| MEDLINE | ID: mdl-34906456
4.
Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar.
Hum Mutat
; 39(11): 1650-1659, 2018 11.
Article
in English
| MEDLINE | ID: mdl-30095202
5.
PMS2 monoallelic mutation carriers: the known unknown.
Genet Med
; 18(1): 13-9, 2016 Jan.
Article
in English
| MEDLINE | ID: mdl-25856668
6.
Further Defining the Role of the Laboratory Genetic Counselor.
J Genet Couns
; 25(4): 786-98, 2016 08.
Article
in English
| MEDLINE | ID: mdl-26895873
7.
Rare deletions at the neurexin 3 locus in autism spectrum disorder.
Am J Hum Genet
; 90(1): 133-41, 2012 Jan 13.
Article
in English
| MEDLINE | ID: mdl-22209245
8.
The utilization of counseling skills by the laboratory genetic counselor.
J Genet Couns
; 24(1): 6-17, 2015 Feb.
Article
in English
| MEDLINE | ID: mdl-25138081
9.
Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation.
J Med Genet
; 50(3): 163-73, 2013 Mar.
Article
in English
| MEDLINE | ID: mdl-23335808
10.
Response to Commercial Genetic Testing and the Future of the Genetic Counseling Profession.
J Genet Couns
; 27(3): 530-532, 2018 06.
Article
in English
| MEDLINE | ID: mdl-29569053
11.
Lynch syndrome and MYH-associated polyposis: review and testing strategy.
J Clin Gastroenterol
; 45(6): 488-500, 2011 Jul.
Article
in English
| MEDLINE | ID: mdl-21325953
12.
Response to ten Broeke and Nielsen.
Genet Med
; 17(8): 684-5, 2015 Aug.
Article
in English
| MEDLINE | ID: mdl-26240979
13.
Familial segregation of a 5q15-q21.2 deletion associated with facial dysmorphism and speech delay.
Clin Case Rep
; 7(6): 1154-1160, 2019 Jun.
Article
in English
| MEDLINE | ID: mdl-31183085
14.
Malignant Peripheral Nerve Sheath Tumor in a Patient With BAP1 Tumor Predisposition Syndrome.
World Neurosurg
; 109: 362-364, 2018 Jan.
Article
in English
| MEDLINE | ID: mdl-29061454
15.
Pathologic findings in breast, fallopian tube, and ovary specimens in non-BRCA hereditary breast and/or ovarian cancer syndromes: a study of 18 patients with deleterious germline mutations in RAD51C, BARD1, BRIP1, PALB2, MUTYH, or CHEK2.
Hum Pathol
; 70: 14-26, 2017 12.
Article
in English
| MEDLINE | ID: mdl-28709830
16.
Genetic testing utilization and the role of the laboratory genetic counselor.
Clin Chim Acta
; 427: 193-5, 2014 Jan 01.
Article
in English
| MEDLINE | ID: mdl-24084506
17.
Genetics of adult glioma.
Cancer Genet
; 205(12): 613-21, 2012 Dec.
Article
in English
| MEDLINE | ID: mdl-23238284
Results
1 -
17
de 17
1
Next >
>>