S. Noblin

发表

Influence of Anchoring on Miscarriage Risk Perception Associated with Amniocentesis

S. Hashmi, Regina Nuccio, J. Mastrobattista, 2015, Journal of Genetic Counseling.

Patients with unexplained mismatch repair deficiency are interested in updated genetic testing

B. Stevens, E. Vilar, S. Noblin, 2020, Hereditary cancer in clinical practice.

Somatic mismatch repair testing in evaluation of Lynch syndrome: The gap between preferred and current practices

E. Vilar, S. Noblin, M. Mork, 2020, Journal of genetic counseling.

Exploring experiences and expectations of prenatal health care and genetic counseling/testing in immigrant Latinas.

N. Zacharias, S. Noblin, G. Palos, 2020, Journal of genetic counseling.

Introduction of cell‐free DNA screening is associated with changes in prenatal genetic counseling indications

B. Stevens, Han-Yang Chen, L. Friel, 2019, Journal of genetic counseling.

Attitudes Towards Prenatal Genetic Counseling, Prenatal Genetic Testing, and Termination of Pregnancy among Southeast and East Asian Women in the United States

S. Peterson, H. Mendez-Figueroa, S. Noblin, 2017, Journal of Genetic Counseling.

Expanded newborn screening in Texas: a survey and educational module addressing the knowledge of pediatric residents

H. Northrup, B. Therrell, S. Noblin, 2009, Genetics in Medicine.

2013 Review and Update of the Genetic Counseling Practice Based Competencies by a Task Force of the Accreditation Council for Genetic Counseling

D. L. Doyle, K. Ormond, E. Petty, 2016, Journal of Genetic Counseling.

Fetal trisomy 21 and the risk of preeclampsia

M. Monga, M. Gambello, A. Vidaeff, 2009, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Evaluating the NCCN Clinical Criteria for Recommending BRCA1 and BRCA2 Genetic Testing in Patients With Breast Cancer.

Diane D. Liu, B. Arun, M. Daniels, 2017, Journal of the National Comprehensive Cancer Network : JNCCN.

The utilization of prenatal microarray: A survey of current genetic counseling practices and barriers

B. Stevens, R. Papanna, David F Rodriguez-Buritica, 2019, Prenatal diagnosis.

Survival of Texas infants born with trisomies 21, 18, and 13

S. Daiger, M. Gambello, J. Hecht, 2010, American journal of medical genetics. Part A.

NSGC Practice Guideline: Prenatal Screening and Diagnostic Testing Options for Chromosome Aneuploidy

S. Noblin, C. Singletary, C. Sullivan, 2013, Journal of Genetic Counseling.

Knowledge and Self-Esteem of Individuals with Neurofibromatosis Type 1 (NF1)

H. Northrup, S. Noblin, S. Hashmi, 2017, Journal of Genetic Counseling.

Is it all Lynch Syndrome? An assessment of family history in individuals with mismatch repair deficient tumors

R. Broaddus, K. Lu, B. Fellman, 2014, Genetics in Medicine.