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Natasha Shur

Showing results (11-20 of 56) with videos related to

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American Journal of Medical Genetics. Part A|July 29, 2003
Craniosynostosis and congenital heart anomalies associated with a maternal deletion of 15q15-22.1Natasha Shur, Janet Cowan, Patricia G Wheeler
Pediatric Annals|March 31, 2025
Rare Disease Growth Monitoring: Improving Early DiagnosisNatasha Shur, Seth Berger, Andrew Dauber, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 20, 2015
The clinical geneticist and the evaluation of failure to thrive versus failure to feedJillian Rabago, Kayt Marra, Nikki Allmendinger, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|September 10, 2020
Further Clinical Delineation of Chromosome 1q21Microduplication Syndrome: Robin Sequence as an Under-Recognized Association in Chromosomal Microdeletions and DuplicationsLauren K Salinero, Natasha Shur, Albert K Oh
Pediatric Annals|September 9, 2025
Incorporating Rare Disease Growth Monitoring Into Routine Practice to Improve Early Recognition and Diagnosis of Genetic ConditionsNatasha Shur, Seth Berger, Andrew Dauber, et al.
Pediatric Annals|April 2, 2026
A Stepwise Approach to Macrocephaly: Clinical Clues to the Rare Diagnosis of PTEN Hamartoma Tumor SyndromeNidhi A Gupta, Natasha Shur, Seth I Berger
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 22, 2020
Society for Pediatric Radiology (SPR) Child Abuse Committee response regarding Miller, Stolfi and Ayoub's flawed theories about child abuse and metabolic bone diseaseStephen D Brown, Joelle A Moreno, Natasha Shur, et al.
Radiology|March 26, 2011
Case 168: rhabdoid predisposition syndrome--familial cancer syndromes in childrenTyler J Harris, John E Donahue, Natasha Shur, et al.
Translational Science of Rare Diseases|November 2, 2020
Lysinuric protein intolerance: Pearls to detect this otherwise easily missed diagnosisFiras Alqarajeh, Jacklyn Omorodion, Kerri Bosfield, et al.
Pediatrics|August 17, 2025
Creation and Evaluation of New Growth Charts With a Gradual Transition From WHO to CDC ValuesCarrie Daymont, Wenke Hwang, Ian M Paul, et al.
Pageof 6

Showing results (11-20 of 56) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics. Part A|July 29, 2003
Craniosynostosis and congenital heart anomalies associated with a maternal deletion of 15q15-22.1Natasha Shur, Janet Cowan, Patricia G Wheeler
Pediatric Annals|March 31, 2025
Rare Disease Growth Monitoring: Improving Early DiagnosisNatasha Shur, Seth Berger, Andrew Dauber, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 20, 2015
The clinical geneticist and the evaluation of failure to thrive versus failure to feedJillian Rabago, Kayt Marra, Nikki Allmendinger, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|September 10, 2020
Further Clinical Delineation of Chromosome 1q21Microduplication Syndrome: Robin Sequence as an Under-Recognized Association in Chromosomal Microdeletions and DuplicationsLauren K Salinero, Natasha Shur, Albert K Oh
Pediatric Annals|September 9, 2025
Incorporating Rare Disease Growth Monitoring Into Routine Practice to Improve Early Recognition and Diagnosis of Genetic ConditionsNatasha Shur, Seth Berger, Andrew Dauber, et al.
Pediatric Annals|April 2, 2026
A Stepwise Approach to Macrocephaly: Clinical Clues to the Rare Diagnosis of PTEN Hamartoma Tumor SyndromeNidhi A Gupta, Natasha Shur, Seth I Berger
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 22, 2020
Society for Pediatric Radiology (SPR) Child Abuse Committee response regarding Miller, Stolfi and Ayoub's flawed theories about child abuse and metabolic bone diseaseStephen D Brown, Joelle A Moreno, Natasha Shur, et al.
Radiology|March 26, 2011
Case 168: rhabdoid predisposition syndrome--familial cancer syndromes in childrenTyler J Harris, John E Donahue, Natasha Shur, et al.
Translational Science of Rare Diseases|November 2, 2020
Lysinuric protein intolerance: Pearls to detect this otherwise easily missed diagnosisFiras Alqarajeh, Jacklyn Omorodion, Kerri Bosfield, et al.
Pediatrics|August 17, 2025
Creation and Evaluation of New Growth Charts With a Gradual Transition From WHO to CDC ValuesCarrie Daymont, Wenke Hwang, Ian M Paul, et al.
Pageof 6