Detalhe da pesquisa
1.
Exploring parents' perceptions of the value of pediatric genetic counseling patient letters: A qualitative study presenting lessons learned.
J Genet Couns
; 30(4): 1168-1180, 2021 08.
Artigo
Inglês
| MEDLINE | ID: mdl-33723917
2.
An update to returning genetic research results to individuals: perspectives of the industry pharmacogenomics working group.
Bioethics
; 29(2): 82-90, 2015 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-24471556
3.
Comparison of willingness and preference for genetic counseling via telemedicine: before vs. during the COVID-19 pandemic.
J Community Genet
; 13(4): 449-458, 2022 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-35794442
4.
Assessing parental understanding of variant reclassification in pediatric neurology and developmental pediatrics clinics.
J Community Genet
; 12(4): 663-670, 2021 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-34558037
5.
AsktheGeneticist: five years of online experience.
Genet Med
; 11(4): 294-304, 2009 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-19282773
6.
The use of role-play to enhance medical student understanding of genetic counseling.
Genet Med
; 10(10): 739-44, 2008 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-18813131
7.
Cancer risk assessment and the genetic counseling process: using hereditary breast and ovarian cancer as an example.
Med Princ Pract
; 17(3): 173-89, 2008.
Artigo
Inglês
| MEDLINE | ID: mdl-18408385
8.
Overlapping phenotype of Wolf-Hirschhorn and Beckwith-Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter).
Am J Med Genet A
; 143A(15): 1760-6, 2007 Aug 01.
Artigo
Inglês
| MEDLINE | ID: mdl-17603794
9.
Pediatric otolaryngologists' use of genetic testing.
Arch Otolaryngol Head Neck Surg
; 133(3): 231-6, 2007 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-17372079
10.
Fate maps of neural crest and mesoderm in the mammalian eye.
Invest Ophthalmol Vis Sci
; 46(11): 4200-8, 2005 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-16249499
11.
Familial transmission of oculoauriculovertebral spectrum (Goldenhar syndrome) is not due to mutations in either EYA1 or SALL1.
Am J Med Genet A
; 149A(3): 535-8, 2009 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-19213029
12.
Isolated facial hemihyperplasia: manifestation of Beckwith-Wiedemann syndrome.
J Craniofac Surg
; 19(1): 279-83, 2008 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-18216702
13.
The use of genetic testing in the evaluation of hearing impairment in a child.
Curr Opin Pediatr
; 17(6): 709-12, 2005 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-16282775
14.
Clefting, amniotic bands, and polydactyly: a distinct phenotype that supports an intrinsic mechanism for amniotic band sequence.
Am J Med Genet A
; 137A(3): 298-301, 2005 Sep 01.
Artigo
Inglês
| MEDLINE | ID: mdl-16088913
15.
Single umbilical artery: what does it mean for the fetus? A case-control analysis of pathologically ascertained cases.
Genet Med
; 6(1): 54-7, 2004.
Artigo
Inglês
| MEDLINE | ID: mdl-14726810