المؤلفون: Folligan, K, Laleye, A, Moumouni, H, Koffi, KS, Yao, GV, Adjagba, M, James, YE, Anoukoum, T, Akakpo-Numado, G, Hazemdji-Nimtche, H, Defolo, A, Darre, T, Amegbor, A, Boukari, BS, Darboux, RB

المصدر: Journal de la Recherche Scientifique de l’Université de Lomé; Vol 14, No 1 (2012): Series D; 67-70

مصطلحات موضوعية: Pseudohermaphrodisme féminin, anomalie du développement sexuel XX, caryotype, sexe social

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=78975075580c::eda81560650ff4f5b2c15d2577d4207a
https://www.ajol.info/index.php/jrsul/article/view/86840

المؤلفون: Folligan, K, Moumouni, H, Laleye, A, Koffi, KS, Yao, GV, Adjagba, M, James, YE, Anoukoum, T, Akakpo-Numado, G, Hazemdji-Nimtche, H, Defolo, A, Darre, T, Amegbor, K, Boukari, BS, Darboux, RB

المصدر: Journal de la Recherche Scientifique de l’Université de Lomé; Vol 14, No 1 (2012): Series D; 51-54

مصطلحات موضوعية: masculine pseudohermaphrodism, anomaly of sexual development XY, karyotype, social sex

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=78975075580c::ef25b4064c6154ca02871edc9ef48997
https://www.ajol.info/index.php/jrsul/article/view/86817

المؤلفون: Folligan, K, Moumouni, H, Laleye, A, Koffi, KS, Yao, GV, Adjagba, M, James, YE, Anoukoum, T, Akakpo-Numado, G, Hazemdji-Nimtche, H, Defolo, A, Darre, T, Amegbor, K, Boukari, BS, Darboux, RB

المصدر: Journal de la Recherche Scientifique de l’Université de Lomé; Vol 14, No 1 (2012): Series D

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=78975075580c::68558b127403f8a070ae197511fe07f4
https://www.ajol.info/index.php/jrsul/article/view/79979

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المؤلفون: Laleye A; Unité de Biologie Humaine, Faculté des Sciences de la Santé, Cotonou, Bénin. cytogen@intnet.bj, Alao MJ, Gbessi G, Adjagba M, Marche M, Coupry I, Redonnet-Vernhet I, Lepreux S, Ayivi B, Darboux RB, Lacombe D, Arveiler B

المصدر: Genetic counseling (Geneva, Switzerland) [Genet Couns] 2008; Vol. 19 (2), pp. 183-92.

نوع المنشور: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Edition Medecine Et Hygiene Country of Publication: Switzerland NLM ID: 9015261 Publication Model: Print Cited Medium: Print ISSN: 1015-8146 (Print) Linking ISSN: 10158146 NLM ISO Abbreviation: Genet Couns Subsets: MEDLINE

مواضيع طبية MeSH: Mutation*, Black People/*genetics , Calcinosis/*genetics , Joint Diseases/*genetics , N-Acetylgalactosaminyltransferases/*genetics, Adolescent ; Adult ; Amelogenesis Imperfecta/genetics ; Amelogenesis Imperfecta/pathology ; Apatites/blood ; Benin ; Calcinosis/pathology ; Fibroblast Growth Factor-23 ; Humans ; Hyperphosphatemia/genetics ; Hyperphosphatemia/pathology ; Joint Diseases/pathology ; Male ; Pedigree ; Siblings ; Polypeptide N-acetylgalactosaminyltransferase

المؤلفون: Houinato D; UFR de Neurologie, Faculté des Sciences de la Santé, Cotonou, Benin., Laleye A, Adjien C, Adjagba M, Sternberg D, Hilbert P, Vallat JM, Darboux RB, Funalot B, Avode DG

المصدر: Neuromuscular disorders : NMD [Neuromuscul Disord] 2007 May; Vol. 17 (5), pp. 419-22. Date of Electronic Publication: 2007 Apr 05.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Pergamon Press Country of Publication: England NLM ID: 9111470 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0960-8966 (Print) Linking ISSN: 09608966 NLM ISO Abbreviation: Neuromuscul Disord Subsets: MEDLINE

مواضيع طبية MeSH: Family Health* , Mutation*, Arginine/*genetics , Calcium Channels/*genetics , Histidine/*genetics , Hypokalemic Periodic Paralysis/*genetics, Adolescent ; Adult ; Africa ; DNA Mutational Analysis ; Female ; Humans ; Hypokalemic Periodic Paralysis/pathology ; Male ; Microscopy, Electron, Transmission ; Middle Aged ; Muscle, Skeletal/pathology ; Muscle, Skeletal/ultrastructure

عنوان ترانسليتريتد: Hybridation in situ en fluorescence et trisomie 13 en mosaïque: un exemple de difficultés de prise en charge des maladies génétiques au Togo.

المؤلفون: Gnamey DK, Dovi-Akué JP, Darboux RB, Laleye A, Adjenou P, Adanlete F

المصدر: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie [Arch Pediatr] 2001 May; Vol. 8 (5), pp. 555.

نوع المنشور: Case Reports; Letter

بيانات الدورية: Publisher: Elsevier Country of Publication: France NLM ID: 9421356 Publication Model: Print Cited Medium: Print ISSN: 0929-693X (Print) Linking ISSN: 0929693X NLM ISO Abbreviation: Arch Pediatr Subsets: MEDLINE

مواضيع طبية MeSH: In Situ Hybridization, Fluorescence*, Chromosomes, Human, Pair 13/*genetics , Trisomy/*genetics, Adult ; Diagnosis, Differential ; Female ; Humans ; Infant, Newborn ; Male ; Togo ; Trisomy/diagnosis

عنوان ترانسليتريتد: Schistosomose et cancer de la vessie dans la vallée de l'Ouémé. Intérêt d'une nouvelle technique de concentration cytologigue et parasitaire à l'aide de la gomme arabique.

المؤلفون: Galley F, Massougbodji A, Aissi-Yehouessi E, Darboux RB, Odoulami F, Sadeler BC

المصدر: Archives d'anatomie et de cytologie pathologiques [Arch Anat Cytol Pathol] 1987; Vol. 35 (2), pp. 101-6.

نوع المنشور: English Abstract; Journal Article

بيانات الدورية: Publisher: Expansion scientifique française Country of Publication: France NLM ID: 7609770 Publication Model: Print Cited Medium: Print ISSN: 0395-501X (Print) Linking ISSN: 0395501X NLM ISO Abbreviation: Arch Anat Cytol Pathol Subsets: MEDLINE

مواضيع طبية MeSH: Schistosoma haematobium/*isolation & purification , Schistosomiasis haematobia/*diagnosis , Urinary Bladder Diseases/*diagnosis , Urinary Bladder Neoplasms/*diagnosis, Adolescent ; Adult ; Benin ; Child ; Child, Preschool ; Female ; Gum Arabic ; Humans ; Male ; Schistosomiasis haematobia/epidemiology ; Schistosomiasis haematobia/pathology ; Urinary Bladder Diseases/epidemiology ; Urinary Bladder Diseases/pathology ; Urinary Bladder Neoplasms/epidemiology ; Urinary Bladder Neoplasms/pathology