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Anne M Slavotinek

Showing results (31-40 of 93) with videos related to

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American Journal of Medical Genetics. Part A|June 16, 2005
Case reports of oculofaciocardiodental syndrome with unusual dental findingsSnehlata Oberoi, Alison E Winder, Jennifer Johnston, et al.
HGG Advances|March 24, 2024
Diagnostic yield after next-generation sequencing in pediatric cardiovascular diseaseAnne M Slavotinek, Michelle L Thompson, Lisa J Martin, et al.
American Journal of Medical Genetics. Part A|October 6, 2012
Special Section. Syndrome-specific growth chartsJudith G Hall, Judith E Allanson, Karen W Gripp, et al.
American Journal of Medical Genetics. Part A|November 12, 2005
Cardiovascular malformations in Fryns syndrome: is there a pathogenic role for neural crest cells?Angela E Lin, Barbara R Pober, Mary P Mullen, et al.
Pediatric Neurology|November 7, 2012
Intraparenchymal hemorrhage in a neonate with cleidocranial dysostosisMarisa A Gardner, Ben C Li, Yvonne W Wu, et al.
American Journal of Medical Genetics. Part A|August 23, 2005
Acro-dermato-ungual-lacrimal-tooth (ADULT) syndrome: report of a child with phenotypic overlap with ulnar-mammary syndrome and a new mutation in TP63Anne M Slavotinek, June Tanaka, Alison Winder, et al.
Clinical Dysmorphology|December 5, 2012
2p16.3 microdeletion with partial deletion of the neurexin-1 gene in a female with developmental delays, short stature, and a congenital diaphragmatic herniaKarla Bermudez-Wagner, Linda J B Jeng, Anne M Slavotinek, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 13, 2018
Private payer coverage policies for exome sequencing (ES) in pediatric patients: trends over time and analysis of evidence citedMichael P Douglas, Stephanie L Parker, Julia R Trosman, et al.
Ophthalmic Genetics|June 22, 2017
Inner retinal dystrophy in a patient with biallelic sequence variants in BRAT1Julius T Oatts, Jacque L Duncan, Creig S Hoyt, et al.
American Journal of Medical Genetics. Part A|October 4, 2011
Congenital diaphragmatic hernia in Smith-Magenis syndrome: a possible locus at chromosome 17p11.2E F Sanford, K Bermudez-Wagner, L J B Jeng, et al.
Pageof 10

Showing results (31-40 of 93) with videos related to

Sort By:
Pageof 10
American Journal of Medical Genetics. Part A|June 16, 2005
Case reports of oculofaciocardiodental syndrome with unusual dental findingsSnehlata Oberoi, Alison E Winder, Jennifer Johnston, et al.
HGG Advances|March 24, 2024
Diagnostic yield after next-generation sequencing in pediatric cardiovascular diseaseAnne M Slavotinek, Michelle L Thompson, Lisa J Martin, et al.
American Journal of Medical Genetics. Part A|October 6, 2012
Special Section. Syndrome-specific growth chartsJudith G Hall, Judith E Allanson, Karen W Gripp, et al.
American Journal of Medical Genetics. Part A|November 12, 2005
Cardiovascular malformations in Fryns syndrome: is there a pathogenic role for neural crest cells?Angela E Lin, Barbara R Pober, Mary P Mullen, et al.
Pediatric Neurology|November 7, 2012
Intraparenchymal hemorrhage in a neonate with cleidocranial dysostosisMarisa A Gardner, Ben C Li, Yvonne W Wu, et al.
American Journal of Medical Genetics. Part A|August 23, 2005
Acro-dermato-ungual-lacrimal-tooth (ADULT) syndrome: report of a child with phenotypic overlap with ulnar-mammary syndrome and a new mutation in TP63Anne M Slavotinek, June Tanaka, Alison Winder, et al.
Clinical Dysmorphology|December 5, 2012
2p16.3 microdeletion with partial deletion of the neurexin-1 gene in a female with developmental delays, short stature, and a congenital diaphragmatic herniaKarla Bermudez-Wagner, Linda J B Jeng, Anne M Slavotinek, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 13, 2018
Private payer coverage policies for exome sequencing (ES) in pediatric patients: trends over time and analysis of evidence citedMichael P Douglas, Stephanie L Parker, Julia R Trosman, et al.
Ophthalmic Genetics|June 22, 2017
Inner retinal dystrophy in a patient with biallelic sequence variants in BRAT1Julius T Oatts, Jacque L Duncan, Creig S Hoyt, et al.
American Journal of Medical Genetics. Part A|October 4, 2011
Congenital diaphragmatic hernia in Smith-Magenis syndrome: a possible locus at chromosome 17p11.2E F Sanford, K Bermudez-Wagner, L J B Jeng, et al.
Pageof 10