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Hiba Risheg

Showing results (1-10 of 15) with videos related to

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Journal of Clinical Gastroenterology|March 11, 2005
Molecular studies of liver disease in erythropoietic protoporphyriaJoseph Bloomer, Yongming Wang, Anuj Singhal, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|April 4, 2002
Ferrochelatase gene mutations in erythropoietic protoporphyria: focus on liver diseaseFu-Ping Chen, Hiba Risheg, Yunying Liu, et al.
Molecular Genetics and Metabolism|October 22, 2003
Genotypic determinants of phenotype in North American patients with erythropoietic protoporphyriaHiba Risheg, Fu-Ping Chen, Joseph R Bloomer
Journal of Clinical Research in Pediatric Endocrinology|July 20, 2017
Response to Growth Hormone Treatment in a Patient with Insulin-Like Growth Factor 1 Receptor DeletionRanim Mahmoud, Ajanta Naidu, Hiba Risheg, et al.
Journal of Pediatric Gastroenterology and Nutrition|July 5, 2006
Biochemical abnormality in erythropoietic protoporphyria: cause and consequencesJoseph R Bloomer, Yongming Wang, Anuj Singhal, et al.
Journal of the Association of Genetic Technologists|June 6, 2026
Laboratory Stewardship Rescues Misordered Familial Targeted Cytogenetic Testing Following Proband Genomic Testing: Case Series ReviewAmanda S Openshaw, Rachel M Lasher, Michelle Q Bosworth, et al.
American Journal of Medical Genetics. Part A|March 5, 2015
Partial monosomy of 11q22.2q22.3 including the SDHD gene in individuals with developmental delayKrishna Yelavarthi, Huong Cabral, Golder N Wilson, et al.
American Journal of Medical Genetics. Part A|May 20, 2011
UPD detection using homozygosity profiling with a SNP genotyping microarrayPeter Papenhausen, Stuart Schwartz, Hiba Risheg, et al.
American Journal of Medical Genetics. Part A|May 3, 2017
6q25.1 (TAB2) microdeletion syndrome: Congenital heart defects and cardiomyopathyAndrew Cheng, Mary Beth P Dinulos, Whitney Neufeld-Kaiser, et al.
American Journal of Medical Genetics. Part A|May 23, 2013
Prenatal diagnosis of two fetuses with deletions of 8p23.1, critical region for congenital diaphragmatic hernia and heart defectsElisabeth A Keitges, Romela Pasion, Rachel D Burnside, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Journal of Clinical Gastroenterology|March 11, 2005
Molecular studies of liver disease in erythropoietic protoporphyriaJoseph Bloomer, Yongming Wang, Anuj Singhal, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|April 4, 2002
Ferrochelatase gene mutations in erythropoietic protoporphyria: focus on liver diseaseFu-Ping Chen, Hiba Risheg, Yunying Liu, et al.
Molecular Genetics and Metabolism|October 22, 2003
Genotypic determinants of phenotype in North American patients with erythropoietic protoporphyriaHiba Risheg, Fu-Ping Chen, Joseph R Bloomer
Journal of Clinical Research in Pediatric Endocrinology|July 20, 2017
Response to Growth Hormone Treatment in a Patient with Insulin-Like Growth Factor 1 Receptor DeletionRanim Mahmoud, Ajanta Naidu, Hiba Risheg, et al.
Journal of Pediatric Gastroenterology and Nutrition|July 5, 2006
Biochemical abnormality in erythropoietic protoporphyria: cause and consequencesJoseph R Bloomer, Yongming Wang, Anuj Singhal, et al.
Journal of the Association of Genetic Technologists|June 6, 2026
Laboratory Stewardship Rescues Misordered Familial Targeted Cytogenetic Testing Following Proband Genomic Testing: Case Series ReviewAmanda S Openshaw, Rachel M Lasher, Michelle Q Bosworth, et al.
American Journal of Medical Genetics. Part A|March 5, 2015
Partial monosomy of 11q22.2q22.3 including the SDHD gene in individuals with developmental delayKrishna Yelavarthi, Huong Cabral, Golder N Wilson, et al.
American Journal of Medical Genetics. Part A|May 20, 2011
UPD detection using homozygosity profiling with a SNP genotyping microarrayPeter Papenhausen, Stuart Schwartz, Hiba Risheg, et al.
American Journal of Medical Genetics. Part A|May 3, 2017
6q25.1 (TAB2) microdeletion syndrome: Congenital heart defects and cardiomyopathyAndrew Cheng, Mary Beth P Dinulos, Whitney Neufeld-Kaiser, et al.
American Journal of Medical Genetics. Part A|May 23, 2013
Prenatal diagnosis of two fetuses with deletions of 8p23.1, critical region for congenital diaphragmatic hernia and heart defectsElisabeth A Keitges, Romela Pasion, Rachel D Burnside, et al.
Pageof 2