kw.\*:("Monogénique")
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The genetic and molecular bases of monogenic disorders affecting proteolytic systemsRICHARD, I.Journal of medical genetics. 2005, Vol 42, Num 7, pp 529-539, issn 0022-2593, 11 p.Article
Lessons from studying monogenic disease for common diseasePELTONEN, Leena; PEROLA, Markus; NAUKKARINEN, Jussi et al.Human molecular genetics (Print). 2006, Vol 15, issn 0964-6906, R67-R74, NSArticle
Comment repérer une obésité génétique ? = How can we identify obesity with genetic origin?POITOU, C; CLEMENT, K.Obésité. 2010, Vol 5, Num 4, pp 103-108, issn 1951-5995, 6 p.Article
Monogenic Mendelian disorders in general neurological practiceLARNER, A. J.International journal of clinical practice (Esher). 2008, Vol 62, Num 5, pp 744-746, issn 1368-5031, 3 p.Article
Monogenic and other unusual causes of diabetes mellitusNAKHLA, Meranda; POLYCHRONAKOS, Constantin.The Pediatric clinics of North America. 2005, Vol 52, Num 6, issn 0031-3955, viii, 1637-150 [15 p.]Article
IDENTITY COEFFICIENTS AND COVARIANCES BETWEEN RELATIVES IN A PARENT-OFFSPRING INBREEDING SYSTEM. = COEFFICIENTS D'IDENTITE ET COVARIANCES ENTRE PARENTS DANS UN SYSTEME DE CONSANGUINITE PARENTS-DESCENDANTSCORNELIUS PL.1975; THEOR. APPL. GENET.; GERM.; DA. 1975; VOL. 46; NO 4; PP. 201-212; BIBL. 12 REF.Article
MUTATION "EPI RETOURNE" (CTO) MODIFIANT LE DEVELOPPEMENT DE L'EPI DE MAISVAKHRUSHEVA EH I.1975; GENETIKA; S.S.S.R.; DA. 1975; VOL. 11; NO 12; PP. 9-14; ABS. ANGL.; BIBL. 1 REF.Article
MONOGENIC DISORDERS.CARTER CO.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 5; PP. 316-320; BIBL. 42 REF.Article
VERIFICATION DE L'HYPOTHESE DE TRANSMISSION MONOGENIQUE D'UN CARACTERE QUANTITATIF SUR LA BASE DE DONNEES DE POPULATIONGINZBURG EH KH; NIKORO ZS.1982; GENETIKA; ISSN 0016-6758; SUN; DA. 1982; VOL. 18; NO 7; PP. 1095-1100; ABS. ENG; BIBL. 1 REF.Article
LIMITS OF THE GENERAL TWO-ALLELE SINGLE LOCUS MODEL WITH INCOMPLETE PENETRANCE.SUAREZ BK; REICH T; TROST J et al.1976; ANN. HUM. GENET.; G.B.; DA. 1976; VOL. 40; NO 2; PP. 231-244; BIBL. 6 REF.Article
DETERMINATION SIMULTANEE DE LA FREQUENCE ALLELIQUE ET DE LA PENETRANCE EN UTILISANT LA FREQUENCE DES PHENOTYPES OBSERVES. IV. FORMULE DES FREQUENCES ALLELIQUES ET DES PENETRANCES PAR LES FREQUENCES PHENOTYPIQUES POUR DIFFERENTS TYPES DE TRANSMISSION MONOGENIQUEKORCHAGIN NV.1980; GENETIKA; ISSN 0016-6758; SUN; DA. 1980; VOL. 16; NO 10; PP. 1834-1843; ABS. ENG; BIBL. 4 REF.Article
Investigating monogenic and complex diseases with pluripotent stem cellsHAO ZHU; MENSCH, M. William; CAHAN, Patrick et al.Nature reviews. Genetics (Print). 2011, Vol 12, Num 4, pp 266-275, issn 1471-0056, 10 p.Article
Monogenic function range resolution radarMOHARIR, P. S; VENKATA RAO, K; VARMA, S. K et al.IEE proceedings. Part F. Communications, radar and signal processing. 1987, Vol 134, Num 6, pp 620-628, issn 0143-7070Article
Genetics of the human obesitiesFUMERON, F.Obésité. 2013, Vol 8, Num 1, pp 22-33, issn 1951-5995, 12 p.Article
Le séquençage de l'exome au secours des maladies génétiques = Exome sequencing applied to monogenic disordersCRIQUI, Audrey; BAULANDE, Sylvain.MS. Médecine sciences. 2010, Vol 26, Num 5, pp 452-454, issn 0767-0974, 3 p.Article
WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in LebanonZALLOUA, Pierre A; AZAR, Sami T; JULIER, Cécile et al.Human molecular genetics (Print). 2008, Vol 17, Num 24, pp 4012-4021, issn 0964-6906, 10 p.Article
Monogenic dyslipidemias: Window on determinants of plasma lipoprotein metabolismHEGELE, Robert A.American journal of human genetics. 2001, Vol 69, Num 6, pp 1161-1177, issn 0002-9297Article
Insights into the molecular correlates modulating functional compensation between monogenic and polygenic disease gene duplicates in humanPODDER, Soumita; TAPASH CHANDRA GHOSH.Genomics (San Diego, Calif.). 2011, Vol 97, Num 4, pp 200-204, issn 0888-7543, 5 p.Article
Thiamine transporter mutation : an example of monogenic diabetes mellitusALZAHRANI, Ali S; BAITEI, Essa; MINGING ZOU et al.European journal of endocrinology. 2006, Vol 155, Num 6, pp 787-792, issn 0804-4643, 6 p.Article
ESTIMATING THE PARAMETERS OF THE INCOMPLETELY PENETRANT SINGLE LOCUS MODEL USING MULTIPLE POPULATIONS.SUAREZ BK; FISHMAN PM; REICH T et al.1977; HUM. HERED.; SWITZ.; DA. 1977; VOL. 27; NO 5; PP. 336-351; BIBL. 7 REF.Article
Vérification de l'hypothèse monogénique par pédigrés de structure arbitraire sélectionnés pour le sujet atteint. II. Problèmes de prédictionAKSENOVICH, T. I; GINZBURG, EH. KH.Genetika. 1986, Vol 22, Num 3, pp 423-433, issn 0016-6758Article
REFUTATION OF THE GENERAL SINGLE-LOCUS MODEL FOR THE ETIOLOGY OF SCHIZOPHRENIAO'ROURKE DH; GOTTESMAN II; SUAREZ BK et al.1982; AMERICAN JOURNAL OF HUMAN GENETICS; ISSN 0002-9297; USA; DA. 1982; VOL. 34; NO 4; PP. 630-649; BIBL. 81 REF.Article
SEXUAL DIMORPHISM AND POLYGENIC INHERITANCE IN MANNURSE GT.1974; S. AFR. J. MED. SCI.; S. AFR.; DA. 1974; VOL. 39; NO 2; PP. 91-97; BIBL. 4REF.Article
ER-associated protein degradation is a common mechanism underpinning numerous monogenic diseases including Robinow syndromeYING CHEN; BELLAMY, William P; SEABRA, Miguel C et al.Human molecular genetics (Print). 2005, Vol 14, Num 17, pp 2559-2569, issn 0964-6906, 11 p.Article
Salivary glands as a potential gene transfer target for gene therapeutics of some monogenetic endocrine disordersVOUTETAKIS, Antonis; BOSSIS, Ioannis; KOK, Marc R et al.Journal of endocrinology. 2005, Vol 185, Num 3, pp 363-372, issn 0022-0795, 10 p.Article