المؤلفون: Peter L. Pearson, Kamlesh Madan

المصدر: Genetics and Molecular Biology, Iss 0 (2018)

مصطلحات موضوعية: Polyploidy, meiosis, human, male, Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572018005009101&lng=en&tlng=en; https://doaj.org/toc/1678-4685

URL الوصول: https://doaj.org/article/1d27b8b58d334121b33cd8aa33b9568b

المؤلفون: Kamlesh, Madan, Konstantin, Miller

المصدر: European Journal of Medical Genetics. 65:104408

مصطلحات موضوعية: Terminology as Topic, Cytogenetic Analysis, Genetics, Humans, Trisomy, Genetic Testing, General Medicine, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b151a6fbbb3621b47d7ff0158623c8e
https://doi.org/10.1016/j.ejmg.2021.104408

المؤلفون: Konstantin Miller, Albert Schinzel, Elisabeth Blennow, Kamlesh Madan

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://www.biologia.uniba.it/eca/NEWSLETTER/NS-17/NL17web.pdf.

وصف الملف: application/pdf

Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.458.1853; http://www.biologia.uniba.it/eca/NEWSLETTER/NS-17/NL17web.pdf

الاتاحة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.458.1853
http://www.biologia.uniba.it/eca/NEWSLETTER/NS-17/NL17web.pdf

المؤلفون: Kamlesh Madan

المصدر: European Journal of Medical Genetics. 63:103971

مصطلحات موضوعية: Genetics, Early embryonic stage, Fetus, Zygote, biology, Mosaicism, Karyotype, fungi, Disorders of Sex Development, Marmoset, Chromosome Disorders, General Medicine, Dizygotic twins, Chimera (genetics), Phenotype, medicine.anatomical_structure, biology.animal, Placenta, medicine, Humans, Genetics (clinical), Organism

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62bbd51783413a9a2c3998db50370d78
https://doi.org/10.1016/j.ejmg.2020.103971

المؤلفون: Kamlesh Madan, Martijn H. Breuning

المصدر: Genetics in Medicine
Genetics in Medicine, 16(6), 425-432

مصطلحات موضوعية: Male, Sex Determination Analysis, business.industry, Prenatal diagnosis, Review, Census, Human genetics, prenatal technology, Prenatal Diagnosis, Humans, sex ratio in India, Medicine, Female, Sex Ratio, Rural area, Socioeconomics, business, China, Genetics (clinical), Sex ratio

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc6633e403176e7a693735965a5807ac
https://doi.org/10.1038/gim.2013.172

المؤلفون: Kamlesh Madan

المساهمون: VU University medical center

المصدر: Prenatal Medicine ISBN: 9780429136221
Prenatal Medicine, 237-272
STARTPAGE=237;ENDPAGE=272;TITLE=Prenatal Medicine
Madan, K 2016, Prenatal diagnosis of chromosome abnormalities . in Prenatal Medicine . Prenatal Medicine, CRC Press, pp. 237-272 .

مصطلحات موضوعية: Gynecology, Edwards syndrome, medicine.medical_specialty, Down syndrome, Chromosome number, business.industry, Turner syndrome, medicine, Chromosome, Prenatal diagnosis, Klinefelter syndrome, medicine.disease, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d6e7774d81e8ae4355d02267e52e24f
https://doi.org/10.3109/9781420016369-19

المؤلفون: Christine E. M. de Die-Smulders, Annemieke H. van der Hout, Egbert Bakker, H.B. Ginjaar, Martijn H. Breuning, Apollonia T. J. M. Helderman-van den Enden, Kamlesh Madan

المساهمون: RS: GROW - R4 - Reproductive and Perinatal Medicine, MUMC+: DA KG Polikliniek (9), Klinische Genetica

المصدر: European Journal of Human Genetics, 21(1), 21-26. Nature Publishing Group
European Journal of Human Genetics, 21(1), 21-6
European Journal of Human Genetics

مصطلحات موضوعية: Male, Duchenne muscular dystrophy, Heterozygote, medicine.medical_specialty, Pediatrics, Genetic counseling, Population, Genetic Counseling, Prenatal diagnosis, Carrier testing, Preimplantation genetic diagnosis, Article, Dystrophin, Pregnancy, Internal medicine, Genetics, medicine, Humans, neonatal screening, carrier testing, education, Preimplantation Diagnosis, POPULATION, preimplantation genetic diagnosis, Genetics (clinical), Netherlands, RISK, education.field_of_study, prenatal diagnosis, business.industry, Incidence, Incidence (epidemiology), Infant, Newborn, PRO051, CARRIERS, medicine.disease, Pedigree, PREVALENCE, Muscular Dystrophy, Duchenne, Endocrinology, Mutation, Female, business

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67589dc8876c283bb2db7aae5aedd465
https://doi.org/10.1038/ejhg.2012.101

المؤلفون: Kamlesh Madan

المصدر: American Journal of Medical Genetics Part A. :947-963

مصطلحات موضوعية: Male, Heterozygote, Derivative chromosome, Genetic counseling, Genetic Counseling, Chromosomal translocation, Chromosomal rearrangement, Biology, Translocation, Genetic, Male infertility, Pregnancy, Middle segment, Prenatal Diagnosis, Chromosome Duplication, Gene duplication, Genetics, medicine, Humans, Genetics (clinical), Chromosome, medicine.disease, Pregnancy Complications, Mutagenesis, Insertional, Infertility, Chromosome Inversion, Female, Chromosome Deletion

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07cb7f268aa9bee01f75383f2373fab7
https://doi.org/10.1002/ajmg.a.35220

المؤلفون: Theo J. Visser, Kerstin Hansson, Frederik J. Hes, Johannes W. A. Smit, I. Shan Rombout-Liem, Kamlesh Madan, Helena Sørensen, Egbert Bakker, Hans Kristian Ploos van Amstel, Karoly Szuhai

المساهمون: Clinical sciences, Medical Genetics, Internal Medicine

المصدر: American Journal of Medical Genetics Part A, 149A(10), 2231-2235. Wiley-Liss Inc.

مصطلحات موضوعية: Male, Heterozygote, medicine.medical_specialty, Aneuploidy, Gonadal dysgenesis, Biology, Y chromosome, mental retardation, Loss of heterozygosity, Thyroid hormone receptor beta, Young Adult, Germline mutation, Hepatolenticular Degeneration, Intellectual Disability, Internal medicine, Genetics, medicine, Humans, hypogonadism, Genetics (clinical), X chromosome, Wilson disease, Chromosome Aberrations, Chromosomes, Human, Y, Mosaicism, Thyroid, Thyroid Hormone Receptors beta, medicine.disease, medicine.anatomical_structure, Endocrinology, thyroid hormone receptor beta (THRB) gene, Karyotyping, Mutation, Gonadal Dysgenesis, Mixed, dicentric Y chromosome

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30f609de2b1b6f1109613ed7a627d639
https://doi.org/10.1002/ajmg.a.33004

المؤلفون: A. W. M. Nieuwint, Rieteke M. van Zalen-Sprock, Kamlesh Madan, Pieter Hummel, Gerard Pals, John M.G. van Vugt, Yvonne M. Heins, Hans Van Der Harten

المساهمون: VU University medical center

المصدر: Prenatal Diagnosis, 19, 72-76. John Wiley and Sons Ltd
Nieuwint, A, van Zalen-Sprock, R M, Hummel, P, Pals, G, van Vugt, J M G, van der Harten, H, Heins, Y & Madan, K 1999, ' 'Identical' twins with discordant karyotypes ', Prenatal Diagnosis, vol. 19, pp. 72-76 . https://doi.org/10.1002/(SICI)1097-0223(199901)19:1<72::AID-PD465>3.0.CO;2-V

مصطلحات موضوعية: Pathology, medicine.medical_specialty, Pregnancy, Fetus, Obstetrics, Obstetrics and Gynecology, Monozygotic twin, Aneuploidy, Prenatal diagnosis, Biology, medicine.disease, Umbilical cord, medicine.anatomical_structure, embryonic structures, medicine, Trisomy, Genetics (clinical), Twin Pregnancy

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78ceefb42e690259311d5a33d54d3048
https://doi.org/10.1002/(sici)1097-0223(199901)19:1<72::aid-pd465>3.0.co;2-v

المؤلفون: Kamlesh Madan, Martijn H. Breuning

المصدر: Genetics in Medicine. 17:89-90

مصطلحات موضوعية: Male, Sex Determination Analysis, business.industry, computer.software_genre, Prenatal Diagnosis, Humans, Female, Sex Ratio, Artificial intelligence, business, Psychology, computer, Genetics (clinical), Natural language processing

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17fe52ba284d970088642f5e8ecb56d0
https://doi.org/10.1038/gim.2014.150

المؤلفون: Kerstin Hansson, de J.W.A. Vries, M.H.E.C. Pieters, K. B. J. Gerssen-Schoorl, Joep H. A. M. Tuerlings, P.M.M. Kastrop, Roel Hordijk, Kamlesh Madan, Jacques C. Giltay, van der M. Blij-Philipsen, Jan A.M. Kremer, Jacques M. J. C. Scheres, G.J.H. Hamers, van der F. Veen, Lutgarde C.P. Govaerts, C.H.J. Tiemessen

المساهمون: Other departments

المصدر: Human reproduction (Oxford, England), 14(2), 318-320. Oxford University Press

مصطلحات موضوعية: Adult, Male, Cytoplasm, medicine.medical_specialty, Pregnancy Rate, medicine.medical_treatment, media_common.quotation_subject, Chromosome Disorders, Fertility, Prenatal diagnosis, Biology, Intracytoplasmic sperm injection, Male infertility, Micromanipulation, Pregnancy, Reference Values, Prenatal Diagnosis, medicine, Humans, Infertility, Male, reproductive and urinary physiology, media_common, Chromosome Aberrations, Gynecology, urogenital system, Rehabilitation, Obstetrics and Gynecology, medicine.disease, Spermatozoa, Fertility clinic, Reproductive Medicine, Karyotyping, Chromosome abnormality, Medical genetics, Female, Follow-Up Studies

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c50c256de94f174d56eb439c1b7c2ef
https://doi.org/10.1093/humrep/14.2.318

المؤلفون: Ralph J. B. Sakkers, Jacques C. Giltay, Gwenda M. Rabelink, Ron Hochstenbach, Kamlesh Madan, Paulien A Terhal, Richard J. Sinke

المصدر: American journal of medical genetics. Part A. (4)

مصطلحات موضوعية: Genetics, Male, Pathology, medicine.medical_specialty, Mosaicism, Aneuploidy, Peripheral Nervous System Diseases, Trisomy, Biology, medicine.disease, Hypoplasia, Uniparental disomy, Cataract, Chromosome 17 (human), Nondisjunction, Cerebellum, Intellectual Disability, medicine, Chromosome abnormality, Humans, Child, Cerebellar hypoplasia, Genetics (clinical), Chromosomes, Human, Pair 17

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de20d2cf699694a3736c4d04bc0f2828
https://pubmed.ncbi.nlm.nih.gov/15481034

المؤلفون: C. Polge, Kamlesh Madan, C. E. Ford

المصدر: Reproduction. 53:395-398

مصطلحات موضوعية: Male, Genetics, Embryology, Swine, Obstetrics and Gynecology, Chromosomal translocation, Cell Biology, Biology, Translocation, Genetic, Domestic pig, Endocrinology, Reproductive Medicine, Karyotyping, Animals

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d461e1981086f4412a0a1f990c453f63
https://doi.org/10.1530/jrf.0.0530395

المؤلفون: Metin Atasu, Kutay Taysi, Sewim Balci, Burhan Say, Martin Bobrow, Kamlesh Madan

المصدر: The Journal of Pediatrics. 82:263-268

مصطلحات موضوعية: Chromosome Aberrations, Genetics, G banding, Infant, Chromosome, Chromosome Disorders, Trisomy, Biology, medicine.disease, Pedigree, Chromosomal crossover, Cytogenetics, D1 trisomy syndrome, Meiosis, Karyotyping, Pediatrics, Perinatology and Child Health, Gene duplication, medicine, Humans, Female, Crossing Over, Genetic, Dermatoglyphics, Chromosomes, Human, 13-15, Chromosomal inversion

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::637d20e4f1183acdd754d4540657589d
https://doi.org/10.1016/s0022-3476(73)80164-7

المؤلفون: Karen Meilinger, Kamlesh Madan, S. Pathak, J.V. Neel, Martin Bobrow, Frank H. Ruddle, Jay A. Tischfield, R.P. Creagan, Suzie Chen, F.A. McMorris, T.R. Chen, M. Hirschi, T. Tsuchimoto, F. Ricciuti, T.C. Hsu, D.M. Cox, A.D. Bloom, T. Utakoji

المصدر: Cytogenetic and Genome Research. 12:199-205

مصطلحات موضوعية: Genetics, Zoology, Karyotype, Biology, Molecular Biology, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::b18fdb506d246df0cde6f07a939aa556
https://doi.org/10.1159/000130455

المؤلفون: Martin Bobrow, Kamlesh Madan, Peter L. Pearson

المصدر: Nature New Biology. 238:122-124

مصطلحات موضوعية: Chromosome Aberrations, Chromosomes, Human, 6-12 and X, Male, Pan troglodytes, Staining and Labeling, Secondary constriction, Differential staining, Chromosomes, Human, 1-3, Hominidae, General Medicine, Biology, Spermatozoa, Molecular biology, General Biochemistry, Genetics and Molecular Biology, Staining, Reannealing, Karyotyping, Centromere, Methods, Animals, Humans, Lymphocytes, Chromosomes, Human, 16-18

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6730fc9fb4c404d3e4922d50bc727dd5
https://doi.org/10.1038/newbio238122a0

المؤلفون: Kamlesh Madan, Martin Bobrow

المصدر: Cytogenetics and cell genetics. 12(3)

مصطلحات موضوعية: Hot Temperature, Staining and Labeling, Acridine orange, Chromosome, Karyotype, Orange (colour), Biology, Hydrogen-Ion Concentration, Fluorescence, Molecular biology, Chromosomes, Staining, chemistry.chemical_compound, chemistry, Biochemistry, Karyotyping, Genetics, Nucleic acid, Methods, Acridines, Humans, Molecular Biology, Genetics (clinical), DNA, Cell Division

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57719dfb49606696e91b1c4b1b6232d4
https://pubmed.ncbi.nlm.nih.gov/4123529

المؤلفون: Kamlesh Madan, Martin Bobrow

المصدر: Cytogenetics and cell genetics. 12(2)

مصطلحات موضوعية: Pan troglodytes, Chromosomes, Human, 19-20, Cytological Techniques, Biology, Giemsa stain, Chromosomes, Species Specificity, Centromeric heterochromatin, Genetics, medicine, Animals, Humans, Trypsin, Chromosomes, Human, 4-5, Molecular Biology, Genetics (clinical), Quinacrine fluorescence, Chromosomes, Human, 16-18, Chromosomes, Human, 6-12 and X, Sex Chromosomes, Staining and Labeling, Chromosomes, Human, 1-3, Karyotype, Molecular biology, Chromatin, Staining, Karyotyping, Chromosomes, Human, 13-15, medicine.drug

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76be2fb1475231694b8dab1a0a639b0a
https://pubmed.ncbi.nlm.nih.gov/4123123

المؤلفون: Kamlesh Madan

المصدر: Human Genetics. 32:141-142

مصطلحات موضوعية: Male, Genetics, Sex Chromosomes, Significant difference, Chromosome, Biology, Human genetics, Phenotype, Karyotyping, Humans, Sex Chromosome Aberrations, Genetics (clinical), X chromosome

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f98db5a308ba3f57cc51a90d82f36e58
https://doi.org/10.1007/bf00291496