المؤلفون: Jacques Senterre, Lucien Lambrechts, Alain Verloes, Lambotte C

المصدر: Scopus-Elsevier
Europe PubMed Central

مصطلحات موضوعية: Male, Microcephaly, Dwarfism, Clenched hands, Genes, Recessive, Osteodysplastic primordial dwarfism, Biology, medicine.disease_cause, Intrauterine growth failure, Disproportionate dwarfism, Pregnancy, Heredity, Diseases in Twins, Genetics, medicine, Humans, Genetics (clinical), Fetal Growth Retardation, Infant, Newborn, Syndrome, Anatomy, medicine.disease, Pedigree, Seckel syndrome, Female

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7db2e4f22127e44323eebe967363157a
https://doi.org/10.1111/j.1399-0004.1987.tb03331.x

المؤلفون: Arnold, H., Dodinval-Versie, J., Lambotte, C., Löhr, G. W., van der Hofstadt, J.

المصدر: Blut: Zeitschrift für die Gesamte Blutforschung. September 1977 35(3):187-193

المؤلفون: Alain Verloes, Jacqueline Bonnivert, P. Dodinval, L. Beco, Lambotte C

المصدر: American Journal of Medical Genetics. 37:119-123

مصطلحات موضوعية: Male, medicine.medical_specialty, Pediatrics, Microcephaly, Genes, Recessive, Telecanthus, Holoprosencephaly, Intellectual Disability, Retrognathia, Internal medicine, medicine, Humans, Abnormalities, Multiple, Hypertelorism, Genetics (clinical), Fetal Growth Retardation, business.industry, Infant, Newborn, Preaxial polydactyly, Infant, Syndrome, Semilobar holoprosencephaly, Aquiline nose, medicine.disease, Endocrinology, Child, Preschool, Face, Female, Genes, Lethal, medicine.symptom, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27c10496ecb14c8c157ccd277ca1aa75
https://doi.org/10.1002/ajmg.1320370128

المؤلفون: Schoos-Barbette, S., Gerard, J., Francotte, N., Lambotte, C.

المصدر: Journal of Inherited Metabolic Disease: Official Journal of the Society for the Study of Inborn Errors of Metabolism. December 1984 7(4):165-167

المؤلفون: Bourguignon, Jean-Pierre, Milet, J., Schoos, R., Franchimont, Paul, Lambotte, C.

المصدر: L'hypothyroïdie congénitale et son dépistage néonatal. Revue Médicale de Liège, 34(19), 816-823.Liège, BelgiumUniversité de Liège. Revue Médicale de Liège. (1979).

مصطلحات موضوعية: Human, Hypothyroidism, Thyroid Hormones, Triiodothyronine, Thyrotropin, Thyroxine, Human health sciences :: Endocrinology, metabolism & nutrition, Sciences de la santé humaine :: Endocrinologie, métabolisme & nutrition

URL الوصول: https://orbi.uliege.be/handle/2268/258495

المؤلفون: Bourguignon, Jean-Pierre, Deby-Dupont, G., Reuter, A., Senterre, J., Lambotte, C., GERARD, Arlette, Franchimont, P.

المصدر: Le dépistage néonatal de la mucoviscidose par dosage radio-immunologique de la trypsine sur l'éluat de sang séché. Revue Médicale de Liège, 39(10), 451-459.Liège, BelgiumUniversité de Liège. Revue Médicale de Liège. (1984).

مصطلحات موضوعية: Cystic Fibrosis, Human, Immunoassay, Infant, Newborn, Trypsin, Mucoviscidosis, Human health sciences :: Pediatrics, Sciences de la santé humaine :: Pédiatrie

URL الوصول: https://orbi.uliege.be/handle/2268/258627

المؤلفون: Lambotte, C., Devlieger, H.

المساهمون: Janssens, P. G., Kivits, M., Vuylsteke, J.

مصطلحات موضوعية: History, Congo-Kinshasa, Burundi, Malnutrition, Sickle cell anemia, Rwanda, Africa, Central, Review, Growth, Mortality, Pediatrics, Children, Nutrition

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______1507::9cea781234d29b842c17953868856645
http://hdl.handle.net/10390/4222

المؤلفون: Schoos R, Lucien Koulischer, Lambotte C, J Dodinval-Versie, Alain Verloes

المصدر: Europe PubMed Central

مصطلحات موضوعية: Percentile, Clinical Biochemistry, Alpha (ethology), Enzyme-Linked Immunosorbent Assay, alpha 1-Antitrypsin Deficiency, medicine, Humans, Dried blood, chemistry.chemical_classification, Detection limit, Chromatography, Spots, medicine.diagnostic_test, biology, business.industry, Liver Diseases, Biochemistry (medical), Infant, Newborn, Enzyme, Phenotype, chemistry, Enzyme inhibitor, Immunoassay, alpha 1-Antitrypsin, Immunology, biology.protein, Isoelectric Focusing, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b87f66955554e201d6697d5c55f75c5
https://pubmed.ncbi.nlm.nih.gov/2049845

المؤلفون: Gilgenkrantz, S., Mujica, P., Gruet, P., Tridon, P., Schweitzer, F., Nivelon-Chevallier, A., Nivelon, J. L., Couillault, G., David, A., Verloes, A., Lambotte, C., Piussan, Ch., Mathieu, M.

المصدر: Clinical Genetics; Oct1988, Vol. 34 Issue 4, p230-245, 16p

المؤلفون: Husquinet, H., Parent, M. T., Schoos-Barbette, S., Dodinval-Versie, J., Lambotte, C., Galacteros, F.

المصدر: Hemoglobin; 1986, Vol. 10 Issue 6, p587-592, 6p