Хайлтын үр дүнгүүд - Lawrence C. Layman
- 33-н 1 - 20 үр дүнгүүдийг харуулж байна
- Дараагийн хуудас руу очих
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Human gene mutations causing infertility -н Lawrence C. Layman
Хэвлэсэн 2002Revisão -
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Role of ART in Imprinting Disorders -н Ali Eroğlu, Lawrence C. Layman
Хэвлэсэн 2012Revisão -
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Clinical and molecular characterization of a large sample of patients with hypogonadotropic hypogonadism -н Balasubramanian Bhagavath, Robert H. Podolsky, Metin Özata, Erol Bolu, David Bick, Anita S. Kulharya, Richard J. Sherins, Lawrence C. Layman
Хэвлэсэн 2006Artigo -
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Liquid Chromatography–Tandem Mass Spectrometry Analysis of Human Adrenal Vein 19-Carbon Steroids Before and After ACTH Stimulation -н Juilee Rege, Yasuhiro Nakamura, Fumitoshi Satoh, Ryo Morimoto, Michael R. Kennedy, Lawrence C. Layman, Seijiro Honma, Hironobu Sasano, William E. Rainey
Хэвлэсэн 2013Artigo -
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Effects of follicle-stimulating hormone and human chorionic gonadotropin on gonadal steroidogenesis in two siblings with a follicle-stimulating hormone β subunit mutation -н Adriana Lofrano‐Porto, Luíz Augusto Casulari, Paula P. Nascimento, Leonardo Giacomini, Luciana Ansaneli Naves, Lucília Domingues Casulari da Motta, Lawrence C. Layman
Хэвлэсэн 2007Artigo -
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Clinical Validation and Diagnostic Utility of Optical Genome Mapping in Prenatal Diagnostic Testing -н Nikhil Sahajpal, Ashis K. Mondal, Timothy Fee, Benjamin Hilton, Lawrence C. Layman, Alex Hastie, Alka Chaubey, Barbara R. DuPont, Ravindra Kolhe
Хэвлэсэн 2023Artigo -
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Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disorders -н Lam Son Nguyen, Hyung‐Goo Kim, Jill A. Rosenfeld, Yiping Shen, James F. Gusella, Yves Lacassie, Lawrence C. Layman, Lisa G. Shaffer, Jozef Gécz
Хэвлэсэн 2013Artigo -
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miRNA-93 Inhibits GLUT4 and Is Overexpressed in Adipose Tissue of Polycystic Ovary Syndrome Patients and Women With Insulin Resistance -н Yen-Hao Chen, Saleh Heneidi, Jung Min Lee, Lawrence C. Layman, David W. Stepp, Gloria Mabel Gamboa, Bo-Shiun Chen, Gregorio D. Chazenbalk, Ricardo Azziz
Хэвлэсэн 2013Artigo -
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FSHβ Gene Mutations in a Female with Partial Breast Development and a Male Sibling with Normal Puberty and Azoospermia -н Lawrence C. Layman, Adriana Lofrano Alves Porto, Jun Xie, Luíz Augusto Casulari Roxo da Motta, Lucília Domingues Casulari da Motta, W Y Weiser, Patrick M. Sluss
Хэвлэсэн 2002Artigo -
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Steric Clash in the SET Domain of Histone Methyltransferase NSD1 as a Cause of Sotos Syndrome and Its Genetic Heterogeneity in a Brazilian Cohort -н Kyungsoo Ha, Priya Anand, Jennifer A. Lee, Julie R. Jones, Chong Ae Kim, Débora Romeo Bertola, Jonathan D. J. Labonne, Lawrence C. Layman, Wolfgang Wenzel, Hyung‐Goo Kim
Хэвлэсэн 2016Artigo
Хайх хэрэгслүүд:
Холбогдох сэдвүүд
Biology
Genetics
Gene
Medicine
Internal medicine
Endocrinology
Hormone
Mutation
Disease
Hypogonadotropic hypogonadism
Coronavirus disease 2019 (COVID-19)
Infectious disease (medical specialty)
Kallmann syndrome
Luteinizing hormone
Pregnancy
Follicle-stimulating hormone
Bioinformatics
Gene expression
Infertility
Missense mutation
Sanger sequencing
Allele
Computer science
Copy-number variation
Gene mutation
Genome
Insulin
Insulin resistance
Intellectual disability
Phenotype