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1
المؤلفون: William J. Rhead, H H Ardinger, Shivanand R. Patil
المصدر: Clinical Genetics. 31:381-385
مصطلحات موضوعية: Monosomy, Isochromosome, Trisomy, Chromosomal translocation, Biology, Long arm, Translocation, Genetic, Genetics, medicine, Humans, Abnormalities, Multiple, Genetics (clinical), Chromosomes, Human, Pair 11, Partial duplication, Chromosome, Karyotype, medicine.disease, Chromosome Banding, Pedigree, Chromosomes, Human, Pair 2, Karyotyping, Female, Chromosome Deletion
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2
المؤلفون: D K, Daily, H H, Ardinger, G E, Holmes
المصدر: American family physician. 61(4)
مصطلحات موضوعية: Diagnosis, Differential, Male, Patient Education as Topic, Fetal Alcohol Spectrum Disorders, Teaching Materials, Fragile X Syndrome, Intellectual Disability, DiGeorge Syndrome, Humans, Infant, Down Syndrome, Magnetic Resonance Imaging
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::f081e61d9c40280bd74645ba84639c21
https://pubmed.ncbi.nlm.nih.gov/10706158 -
3
المؤلفون: A E, Lin, H H, Ardinger, R H, Ardinger, C, Cunniff, R I, Kelley
المصدر: American journal of medical genetics. 68(3)
مصطلحات موضوعية: Heart Defects, Congenital, Male, Phenotype, Humans, Female, Smith-Lemli-Opitz Syndrome
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4
المؤلفون: R, Shiang, A C, Lidral, H H, Ardinger, K H, Buetow, P A, Romitti, R G, Munger, J C, Murray
المصدر: American journal of human genetics. 53(4)
مصطلحات موضوعية: Adult, Male, Adolescent, Base Sequence, Molecular Sequence Data, Infant, Transforming Growth Factor alpha, Cleft Palate, stomatognathic diseases, Child, Preschool, Humans, Female, Child, Sequence Alignment, Polymorphism, Restriction Fragment Length, DNA Primers, Retrospective Studies, Research Article
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::157d2e34f89ab364db840439be46b7bd
https://pubmed.ncbi.nlm.nih.gov/8105683 -
5
المؤلفون: R C, Hennekam, M J, Van Schooneveld, H H, Ardinger, M J, Van Den Boogaard, D, Friedburg, S, Rudnik-Schoneborn, J H, Seguin, K B, Weatherstone, D, Wittebol-Post, P, Meinecke
المصدر: Clinical dysmorphology. 2(4)
مصطلحات موضوعية: Adult, Male, Adolescent, Developmental Disabilities, Infant, Dwarfism, Syndrome, Child, Preschool, Face, Humans, Abnormalities, Multiple, Female, Child, Follow-Up Studies
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::9f9dab2b6f653fd091c6845e13786c77
https://pubmed.ncbi.nlm.nih.gov/7508316 -
6
المؤلفون: D. Friedburg, P. Meinecke, J. H. Seguin, H. H. Ardinger, Raoul C.M. Hennekam, S. Rudnik-Schoneborn, M. J. van den Boogaard, M. J. van Schooneveld, D. Wittebol-Post, K. B. Weatherstone
المساهمون: Other departments
المصدر: Clinical dysmorphology, 2(4), 283-300. Lippincott Williams and Wilkins
مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, business.industry, General Medicine, medicine.disease, Pathology and Forensic Medicine, Intrauterine death, Developmental retardation, Original report, Short-limb dwarfism, Pediatrics, Perinatology and Child Health, Peters-plus syndrome, Medicine, Anatomy, business, Genetics (clinical)
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9598f740c4628d9d3c626733a0f8e5ae
https://doi.org/10.1097/00019605-199310000-00001 -
7
المؤلفون: H H, Ardinger, J A, Bartley
المصدر: Journal of craniofacial genetics and developmental biology. 8(1)
مصطلحات موضوعية: Male, Child, Preschool, Face, Infant, Newborn, Microcephaly, Brain, Humans, Infant, Abnormalities, Multiple, Female, Child, Pedigree
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::d64bd658b6b1e7f3828eff5103d00940
https://pubmed.ncbi.nlm.nih.gov/3209679 -
8
المؤلفون: Jeffrey C. Murray, K.M. Rose, H. H. Ardinger, Y. Yamada
مصطلحات موضوعية: Genetics, Polymorphism, Genetic, biology, DNA–DNA hybridization, EcoRI, DNA Restriction Enzymes, Molecular biology, Gene mapping, Genes, biology.protein, Humans, pUC19, Laminin, BamHI, Restriction fragment length polymorphism, Deoxyribonucleases, Type II Site-Specific, Allele frequency, Chromosomes, Human, Pair 7, Polymorphism, Restriction Fragment Length, Genomic organization
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41ab0c3f1e93fdf5252dd02b6f7dd978
https://europepmc.org/articles/PMC338620/ -
9
المؤلفون: R. J. M. Gardner, J. W. Hanson, V. V. Lonasescu, H. H. Ardinger, D. J. Skorton, L. T. Mahoney, M. N. Hart, E. F. Rose, W. L. Smith, M. S. Florentine, R. L. Hinrichs, James F. Reynolds
المصدر: American journal of medical genetics. 27(1)
مصطلحات موضوعية: Cardiomyopathy, Dilated, Male, medicine.medical_specialty, Pathology, Adolescent, Cardiomyopathy, Internal medicine, Biopsy, medicine, Cardiac biopsy, Humans, Child, Genetics (clinical), Aged, Genes, Dominant, medicine.diagnostic_test, business.industry, Muscles, Myocardium, Heterozygote advantage, Dilated cardiomyopathy, Arrhythmias, Cardiac, Middle Aged, medicine.disease, Pedigree, Skeletal muscle biopsy, Endocrinology, Echocardiography, Concomitant, Proximal weakness, Female, business
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10دورية أكاديمية
المؤلفون: Morris HL; Department of Otolaryngology-Head and Neck Surgery, University of Iowa, Iowa City., Bardach J, Ardinger H, Jones D, Kelly KM, Olin WH, Wheeler J
المصدر: Plastic and reconstructive surgery [Plast Reconstr Surg] 1993 Oct; Vol. 92 (5), pp. 842-51.
نوع المنشور: Journal Article
بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 1306050 Publication Model: Print Cited Medium: Print ISSN: 0032-1052 (Print) Linking ISSN: 00321052 NLM ISO Abbreviation: Plast Reconstr Surg Subsets: MEDLINE
مواضيع طبية MeSH: Cleft Palate/*surgery, Adolescent ; Adult ; Child ; Child, Preschool ; Cleft Palate/complications ; Cleft Palate/genetics ; Ear Diseases/etiology ; Female ; Humans ; Male ; Orthodontics ; Speech Disorders/etiology ; Treatment Outcome
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