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1
المؤلفون: Jodi D. Hoffman, Kelly Kennelly, Linda Kleeman, Engela Honey, William Reardon
المصدر: Clinical Dysmorphology. 24:128-131
مصطلحات موضوعية: Male, Gynecology, Abortion, Habitual, medicine.medical_specialty, Pregnancy, business.industry, Obstetrics, MEDLINE, Hypercoiled Umbilical Cord, General Medicine, Abortion, medicine.disease, Umbilical Cord, Pathology and Forensic Medicine, Sex Factors, Sex factors, Pediatrics, Perinatology and Child Health, Recurrent miscarriage, medicine, Humans, Female, Anatomy, business, Genetics (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5dcb0fcbc02f85492c09d65e874fe73Test
https://doi.org/10.1097/mcd.0000000000000084Test -
2
المؤلفون: K. Cherry Liu, Waasila Jassat, Mansour Farahani, Namiwnga Chintu, Elizabeth M. Stringer, Richard Marlink, Jessica Joseph, Tshililo Mashamba, Michelle Gill, Muthuhadini Patience Mawela, Engela Honey, Nienke Van Schaik
مصطلحات موضوعية: Adult, medicine.medical_specialty, Adolescent, Immunology, Population, Developing country, Zambia, HIV Infections, Article, Congenital Abnormalities, South Africa, Young Adult, Acquired immunodeficiency syndrome (AIDS), Pregnancy, Antiretroviral Therapy, Highly Active, medicine, Prevalence, Immunology and Allergy, Humans, Young adult, Pregnancy Complications, Infectious, Psychiatry, Pregnancy outcomes, education, education.field_of_study, business.industry, Public health, Infant, Newborn, Pregnancy Outcome, Infant, Middle Aged, medicine.disease, Infectious Diseases, Anti-Retroviral Agents, Premature birth, Family medicine, Premature Birth, Female, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59f1e86cf8f78e6b1ae1d0888bfe16a9Test
https://europepmc.org/articles/PMC5454497Test/ -
3
المؤلفون: C Lord, E Bekker, Patrick D. Brophy, Engela Honey, LC Snyman, Richard M. Raymond, J Clarke
المصدر: Clinical genetics. 70(1)
مصطلحات موضوعية: Male, medicine.medical_specialty, Hearing loss, Nonsense mutation, Biology, medicine.disease_cause, Kidney, Genetic analysis, White People, South Africa, Pregnancy, Internal medicine, Genetics, Homologous chromosome, medicine, Ethnicity, Humans, Ear, External, Hearing Loss, Gene, Genetics (clinical), Potter Syndrome, Branchio-oto-renal syndrome, Mutation, Base Sequence, Infant, Newborn, Intracellular Signaling Peptides and Proteins, Infant, Nuclear Proteins, DNA, medicine.disease, Pedigree, Endocrinology, Phenotype, Codon, Nonsense, Female, medicine.symptom, Protein Tyrosine Phosphatases, Branchio-Oto-Renal Syndrome
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b94aa79a4d256c35549414f93b25454Test
https://pubmed.ncbi.nlm.nih.gov/16813606Test