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Mahmoud Aarabi

Showing results (21-30 of 47) with videos related to

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Human Molecular Genetics|January 24, 2018
Testicular MTHFR deficiency may explain sperm DNA hypomethylation associated with high dose folic acid supplementationMahmoud Aarabi, Karen E Christensen, Donovan Chan, et al.
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|September 9, 2010
Polymorphisms of plasminogen activator inhibitor-1, angiotensin converting enzyme and coagulation factor XIII genes in patients with recurrent spontaneous abortionMahmoud Aarabi, Toktam Memariani, Soheila Arefi, et al.
American Journal of Medical Genetics. Part A|October 23, 2024
Recurrent Xp22.31-Yq11 Unbalanced Translocations: Molecular Diagnosis and Clinical Implications in Three FamiliesMarwa Daghsni, Elizabeth Sheehan, Suneeta Madan-Khetarpal, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 30, 2024
Laboratory testing for preconception/prenatal carrier screening: A technical standard of the American College of Medical Genetics and Genomics (ACMG)Saurav Guha, Honey V Reddi, Mahmoud Aarabi, et al.
Human Reproduction (Oxford, England)|February 10, 2018
Chromosomal instability in women with primary ovarian insufficiencySunita Katari, Mahmoud Aarabi, Angela Kintigh, et al.
Psychiatric Genetics|July 15, 2022
Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspotsMahmoud Aarabi, Jacqueline Baumann, Melanie Babcock, et al.
Prenatal Diagnosis|November 25, 2022
Prenatal and fetal diagnosis of trisomy 18 after low-risk cell-free fetal DNA screening: A report of four casesElizabeth Sheehan, Victoria Bacon, Seth Lascurain, et al.
Plos One|March 20, 2012
The testicular and epididymal expression profile of PLCζ in mouse and human does not support its role as a sperm-borne oocyte activating factorMahmoud Aarabi, Yang Yu, Wei Xu, et al.
Acta Gastro-Enterologica Belgica|November 12, 2009
Diagnostic value of antineutrophil cytoplasmic antibodies and anti-Saccharomyces cerevisiae antibody in Iranian patients with inflammatory bowel diseaseAli Bahari, Mahmoud Aarabi, Mohsen Aarabi, et al.
Clinical Genetics|October 3, 2020
Copy number alterations involving 59 ACMG-recommended secondary findings genesSvetlana A Yatsenko, Mahmoud Aarabi, Jie Hu, et al.
Pageof 5

Showing results (21-30 of 47) with videos related to

Sort By:
Pageof 5
Human Molecular Genetics|January 24, 2018
Testicular MTHFR deficiency may explain sperm DNA hypomethylation associated with high dose folic acid supplementationMahmoud Aarabi, Karen E Christensen, Donovan Chan, et al.
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|September 9, 2010
Polymorphisms of plasminogen activator inhibitor-1, angiotensin converting enzyme and coagulation factor XIII genes in patients with recurrent spontaneous abortionMahmoud Aarabi, Toktam Memariani, Soheila Arefi, et al.
American Journal of Medical Genetics. Part A|October 23, 2024
Recurrent Xp22.31-Yq11 Unbalanced Translocations: Molecular Diagnosis and Clinical Implications in Three FamiliesMarwa Daghsni, Elizabeth Sheehan, Suneeta Madan-Khetarpal, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 30, 2024
Laboratory testing for preconception/prenatal carrier screening: A technical standard of the American College of Medical Genetics and Genomics (ACMG)Saurav Guha, Honey V Reddi, Mahmoud Aarabi, et al.
Human Reproduction (Oxford, England)|February 10, 2018
Chromosomal instability in women with primary ovarian insufficiencySunita Katari, Mahmoud Aarabi, Angela Kintigh, et al.
Psychiatric Genetics|July 15, 2022
Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspotsMahmoud Aarabi, Jacqueline Baumann, Melanie Babcock, et al.
Prenatal Diagnosis|November 25, 2022
Prenatal and fetal diagnosis of trisomy 18 after low-risk cell-free fetal DNA screening: A report of four casesElizabeth Sheehan, Victoria Bacon, Seth Lascurain, et al.
Plos One|March 20, 2012
The testicular and epididymal expression profile of PLCζ in mouse and human does not support its role as a sperm-borne oocyte activating factorMahmoud Aarabi, Yang Yu, Wei Xu, et al.
Acta Gastro-Enterologica Belgica|November 12, 2009
Diagnostic value of antineutrophil cytoplasmic antibodies and anti-Saccharomyces cerevisiae antibody in Iranian patients with inflammatory bowel diseaseAli Bahari, Mahmoud Aarabi, Mohsen Aarabi, et al.
Clinical Genetics|October 3, 2020
Copy number alterations involving 59 ACMG-recommended secondary findings genesSvetlana A Yatsenko, Mahmoud Aarabi, Jie Hu, et al.
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