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Hoffman, Jodi D.
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1

Neonatal arrhythmias in Turner syndrome: a case report and ..:

Choi, Yeyoon ; Hoffman, Jodi ; Alarcon, Lizzeth...
European Heart Journal - Case Reports.  5 (2021)  4 - p. , 2021
Link: https://doi.org/10.1093/..
 
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2

Complexities of Clinical Genetics Consultation: An Interpro..:

Hoffman, Jodi D. ; Thompson, Rachel ; Swenson, Kathleen B..
MedEdPORTAL.  , 2020
Link: https://doi.org/10.15766..
 
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3

Evaluation and classification of severity for 176 genes on ..:

Arjunan, Aishwarya ; Bellerose, Holly ; Torres, Raul...
Prenatal Diagnosis.  40 (2020)  10 - p. 1246-1257 , 2020
Link: https://doi.org/10.1002/..
 
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4

Response to Knoppers et al:

David, Karen L. ; Best, Robert G. ; Brenman, Leslie Manace...
Genetics in Medicine.  21 (2019)  10 - p. 2403 , 2019
Link: https://doi.org/10.1038/..
 
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5

Patient re-contact after revision of genomic test results: ..:

David, Karen L. ; Best, Robert G. ; Brenman, Leslie Manace...
Genetics in Medicine.  21 (2019)  4 - p. 769-771 , 2019
Link: https://doi.org/10.1038/..
 
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6

Urogenital and pelvic complications in the Ehlers‐Danlos sy..:

Gilliam, Elizabeth ; Hoffman, Jodi D. ; Yeh, Gloria
Clinical Genetics.  97 (2019)  1 - p. 168-178 , 2019
Link: https://doi.org/10.1111/..
 
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7

17-β-hydroxysteroid dehydrogenase type 3 deficiency: Identi..:

Sullivan, Catherine A. ; Hoffman, Jodi D. ; Safer, Joshua D.
Journal of Clinical and Translational Endocrinology: Case Reports.  7 (2018)  - p. 5-7 , 2018
Link: https://doi.org/10.1016/..
 
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8

Prenatal presentation of 49,XXXXY syndrome:

Stover, Megan W. ; Cowan, Janet ; Cross, Leah..
Prenatal Diagnosis.  37 (2017)  11 - p. 1176-1178 , 2017
Link: https://doi.org/10.1002/..
 
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9

Expanding the SPECC1L mutation phenotypic spectrum to inclu..:

Bhoj, Elizabeth J. ; Li, Dong ; Harr, Margaret H....
American Journal of Medical Genetics Part A.  167 (2015)  11 - p. 2497-2502 , 2015
Link: https://doi.org/10.1002/..
 
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10

OTX2 Duplication Is Implicated in Hemifacial Microsomia:

Zielinski, Dina ; Markus, Barak ; Sheikh, Mona...
PLoS ONE.  9 (2014)  5 - p. e96788 , 2014
Link: https://doi.org/10.1371/..
 
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11

The Ashkenazi Jewish carrier screening panel: evolution, st..:

Hoffman, Jodi D. ; Park, Jessica J. ; Schreiber‐Agus, Nicole...
Prenatal Diagnosis.  34 (2014)  12 - p. 1161-1167 , 2014
Link: https://doi.org/10.1002/..
 
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12

Knowledge, attitudes, and barriers to carrier screening for..:

Warsch, Jessica R. L. ; Warsch, Sean ; Herman, Elizabeth...
Journal of Community Genetics.  5 (2014)  3 - p. 223-231 , 2014
Link: https://doi.org/10.1007/..
 
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13

Next‐generationDNAsequencing ofHEXA: a step in the right di..:

Hoffman, Jodi D. ; Greger, Valerie ; Strovel, Erin T....
Molecular Genetics & Genomic Medicine.  1 (2013)  4 - p. 260-268 , 2013
Link: https://doi.org/10.1002/..
 
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14

3q26.33–3q27.2 microdeletion: A new microdeletion syndrome?:

Mandrile, Giorgia ; Dubois, Anna ; Hoffman, Jodi D....
European Journal of Medical Genetics.  56 (2013)  4 - p. 216-221 , 2013
Link: https://doi.org/10.1016/..
 
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15

More Than Just Skin Deep: Faciocutaneous Clues to Genetic S..:

Shen, Zhu ; Hoffman, Jodi D. ; Hao, Fei.
The Oncologist.  17 (2012)  7 - p. 930-936 , 2012
Link: https://doi.org/10.1634/..
 
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