Detalhe da pesquisa
1.
The 2019 medical genetics workforce: A focus on laboratory geneticists.
Genet Med
; 25(6): 100834, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36999554
2.
Vascular aneurysms in Ehlers-Danlos syndrome subtypes: A systematic review.
Clin Genet
; 103(3): 261-267, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36210598
3.
The 2019 US medical genetics workforce: a focus on clinical genetics.
Genet Med
; 23(8): 1458-1464, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33941882
4.
"It's a Little Different for Men"-Sponsorship and Gender in Academic Medicine: a Qualitative Study.
J Gen Intern Med
; 36(1): 1-8, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32601927
5.
A Cost Analysis of Universal versus Targeted Cholesterol Screening in Pediatrics.
J Pediatr
; 196: 201-207.e2, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29703359
6.
High-Risk Palliative Care Patients' Knowledge and Attitudes about Hereditary Cancer Testing and DNA Banking.
J Genet Couns
; 27(4): 834-843, 2018 08.
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em Inglês
| MEDLINE | ID: mdl-29204810
7.
Family Ties: The Role of Family Context in Family Health History Communication About Cancer.
J Health Commun
; 21(3): 346-55, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26735646
8.
Horizontal integration of OMIM across the medical school preclinical curriculum for early reinforcement of clinical genetics principles.
Genet Med
; 17(2): 158-63, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25032988
9.
What women think: cancer causal attributions in a diverse sample of women.
J Psychosoc Oncol
; 33(1): 48-65, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25398057
10.
Youth with special health care needs: transition to adult health care services.
Matern Child Health J
; 17(10): 1744-52, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23160763
11.
Prolyl 3-hydroxylase 1 and CRTAP are mutually stabilizing in the endoplasmic reticulum collagen prolyl 3-hydroxylation complex.
Hum Mol Genet
; 19(2): 223-34, 2010 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19846465
12.
The Coffin-Siris syndrome: a proposed diagnostic approach and assessment of 15 overlapping cases.
Am J Med Genet A
; 158A(8): 1865-76, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22711679
13.
Monochorionic twins with 15q26.3 duplication presenting with selective intrauterine growth restriction and discordant cardiac anomalies: A case report.
Mol Genet Genomic Med
; 10(8): e1947, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35795918
14.
Genetic risk, perceived risk, and cancer worry in daughters of breast cancer patients.
J Genet Couns
; 20(2): 157-64, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21132457
15.
Demographic and socioeconomic trends in DNA banking utilization in the USA.
J Community Genet
; 12(4): 593-602, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34185264
16.
Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations.
Hum Mutat
; 31(10): 1142-54, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20672375
17.
Exploring hereditary cancer among dying cancer patients--a cross-sectional study of hereditary risk and perceived awareness of DNA testing and banking.
J Genet Couns
; 19(5): 497-525, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20680422
18.
A genetic perspective on infant mortality.
South Med J
; 103(5): 440-4; quiz 445-6, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20375941
19.
GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype.
Hum Mutat
; 30(5): 724-33, 2009 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19338053
20.
Palliative care and genetics: personalized medicine for the patient and family.
Eur J Hum Genet
; 32(1): 8-9, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37607990