Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("LE MERRER, M")

Document Type [dt]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 110

  • Page / 5
Export

Selection :

  • and

POSSUM : diagnostic assisté par ordinateur en génétique médicale = POSSUM: computer-assisted diagnosis in medical geneticsLE MERRER, M.La Revue du praticien (Paris). 1992, Vol 42, Num 3, issn 0035-2640, p. 342Article

De la symbolique des pastourelles méridionales in Intersignes nantais . Mélanges de littératures offert à Madame de la GaranderieLE MERRER, M.Textes et Langages. 1987, Num 14, pp 117-129, issn 0248-4579Article

CONSEIL GENETIQUE ET DIAGNOSTIC ANTENATALBRIARD ML; FREZAL J; KAPLAN J et al.1982; REV. INT. PEDIATR.; ISSN 0048-8135; FRA; DA. 1982; NO 121; PP. 23-38; 11 P.; ABS. ENG; BIBL. 12 REF.Article

COMPORTEMENT DES CONSULTATIONS DE GENETIQUE EN FONCTION DU MILIEU SOCIO-PROFESSIONNELBRIARD ML; KAPLAN J; LE MERRER M et al.1981; J. GENET. HUM.; ISSN 0021-7743; CHE; DA. 1981; VOL. 29; NO 3; PP. 349-357; BIBL. 6 REF.Article

Cartilage hair hypoplasia in infancy : a misleading chondrodysplasiaLE MERRER, M; MAROTEAUX, P.European journal of pediatrics. 1991, Vol 150, Num 12, pp 847-851, issn 0340-6199Article

LES MALFORMATIONS CONGENITALESFREZAL J; BRIARD ML; LE MERRER M et al.1982; REV. INT. PEDIATR.; ISSN 0048-8135; FRA; DA. 1982; NO 121; PP. 9-15; 5 P.; ABS. ENG; BIBL. 13 REF.Article

GenochondromatosisLE MERRER, M; FRESSINGER, P; MAROTEAUX, P et al.Journal of medical genetics. 1991, Vol 28, Num 7, pp 485-489, issn 0022-2593Article

Dysplasie ectodermique et ectrodactylie familiale = Ectodermal dysplasia and familial ectrodactylyPREDINE-HUG, F; LE MERRER, M; FREZAL, J et al.Archives françaises de pédiatrie. 1984, Vol 41, Num 1, pp 49-50, issn 0003-9764Article

ANOMALIES GRAVIDIQUES, SIGNES D'APPEL DE LA DYSTROPHIE MYOTONIQUE CONGENITALE DE STEINERTBRIARD ML; LE MERRER M; GOUTTIERES F et al.1980; J. GENET. HUM.; ISSN 0021-7743; CHE; DA. 1980; VOL. 28; NO 3; PP. 189-194; BIBL. 8 REF.Article

ETUDE EPIDEMIOLOGIQUE ET GENETIQUE DU SPINA BIFIDALE MERRER M; BRIARD ML; DEMENAIS F et al.1980; ARCH. FR. PEDIATR.; ISSN 0003-9764; FRA; DA. 1980; VOL. 37; NO 8; PP. 521-525; ABS. ENG; BIBL. 32 REF.Article

Scalp defect, nipples absence and ears abnormalities : an other case of Finlay syndromeLE MERRER, M; RENIER, D; BRIARD, M. L et al.Genetic counseling. 1991, Vol 2, Num 4, pp 233-236, issn 1015-8146Article

BBBG syndrome or Opitz syndrome: new familyVERLOES, A; LE MERRER, M; BRIARD, M.-L et al.American journal of medical genetics. 1989, Vol 34, Num 3, pp 313-316, issn 0148-7299Article

Le conseil génétique pour les cardiopathies congénitales = Genetic counseling for congenital heart diseasesBRIARD, M. L; LE MERRER, M.L'Information cardiologique. 1993, Vol 17, Num 3, pp 109-115, issn 0220-2476Article

Dwarfism with gloomy face : a new syndrome with features of 3-M syndromeLE MERRER, M; BRAUNER, R; MAROTEAUX, P et al.Journal of medical genetics. 1991, Vol 28, Num 3, pp 186-191, issn 0022-2593Article

Pachydysostosis of the fibulaMAROTEAUX, P; FREISINGER, P; LE MERRER, M et al.Journal of bone and joint surgery. British volume. 1991, Vol 73, Num 5, pp 842-845, issn 0301-620XArticle

Syndromal and nonsyndromal primary trigonocephaly : Analysis of a series of 237 patientsLAJEUNIE, E; LE MERRER, M; MARCHAC, D et al.American journal of medical genetics. 1998, Vol 75, Num 2, pp 211-215, issn 0148-7299Article

Dyssegmental dysplasia with glaucomaMAROTEAUX, P; MANOUVRIER, S; BONAVENTURE, J et al.American journal of medical genetics. 1996, Vol 63, Num 1, pp 46-49, issn 0148-7299Article

Lethal progeroid syndrome with osteolysis : case reportLE MERRER, M; GUILLOT, M; BRIARD, M.-L et al.Annales de génétique (Paris). 1991, Vol 34, Num 2, pp 82-84, issn 0003-3995Article

Impact du conseil génétique sur la fécondité des couples = Influence of genetic counseling on conjugal fertilityBRIARD, M. L; KAPLAN, J; LE MERRER, M et al.Journal de génétique humaine. 1984, Vol 32, Num 4, pp 257-263, issn 0021-7743Article

New insights in congenital bowing of the femoraCORMIER-DAIRE, V; GENEVIEVE, D; MUNNICH, A et al.Clinical genetics. 2004, Vol 66, Num 3, pp 169-176, issn 0009-9163, 8 p.Article

Diagnostic prénatal des gros reins hyperéchogènes = Prenatal diagnosis of enlarged hyperechoic kidneysJURESCO, A; DOMMERGUES, M; LE MERRER, M et al.Annales de pédiatrie (Paris). 1995, Vol 42, Num 10, pp 612-617, issn 0066-2097Article

Recessive metaphyseal dysplasia without hypotrichosis. A syndrome clinically distinct from McKusick cartilage-hair hypoplasiaVERLOES, A; PIERARD, G. E; LE MERRER, M et al.Journal of medical genetics. 1990, Vol 27, Num 11, pp 693-696, issn 0022-2593, 4 p.Article

Acrofacial dysostosesLE MERRER, M; CIKULI, M; RIBIER, J et al.American journal of medical genetics. 1989, Vol 33, Num 3, pp 318-322, issn 0148-7299Article

Le conseil génétique: indications, problèmes et perspectives = Genetic counselling: indications, problems and prospectsBRIARD, M. L; KAPLAN, J; LE MERRER, M et al.Archives françaises de pédiatrie. 1985, Vol 42, Num 3, pp 151-157, issn 0003-9764Article

Place du diagnostic prénatal en consultation de génétique (1982-1983) = Place of prenatal diagnosis in a medical genetic departmentBRIARD, M. L; KAPLAN, J; LE MERRER, M et al.Journal de génétique humaine. 1985, Vol 33, Num 2, pp 187-195, issn 0021-7743Article

  • Page / 5