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au.\*:("EMMERY L")

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THERAPEUTIC EFFECT OF PIMOZIDE IN CONGENITAL GENERALIZED LIPODYSTROPHYEMMERY L; TIMMERMANS J; FRANCOIS B et al.1979; ACTA PAEDIATR. BELG.; BEL; DA. 1979; VOL. 32; NO 3; PP. 209-215; BIBL. 30 REF.Article

Dysplasia epiphysealis capitis femoris? A longitudinal observationEMMERY, L; TIMMERMANI, J; LEROY, J. G et al.European journal of pediatrics. 1983, Vol 140, Num 4, pp 345-347, issn 0340-6199Article

THE WOLF-HIRSCHHORN SYNDROME. DELETION OF THE SHORT ARM OF CHROMOSOME 4FRYNS JP; FRANCOIS B; TIMMERMANS J et al.1979; ACTA PAEDIATR. BELG.; BEL; DA. 1979; VOL. 32; NO 2; PP. 135-139; BIBL. 12 REF.Article

TRICHO-RHINO-PHALANGEAL SYNDROME TYPE II: LANGER-GIEDION SYNDROME IN A 2.5 YEARS-OLD BOYFRYNS SP; EMMERY L; TIMMERMANS S et al.1980; J. GENET. HUM.; CHE; DA. 1980; VOL. 28; NO 1; PP. 53-56; ABS. FRE; BIBL. 2 REF.Article

RING CHROMOSOME 15 SYNDROMEFRYNS JP; TIMMERMANS J; D'HONDT F et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 51; NO 1; PP. 43-48; BIBL. 9 REF.Article

PRIMARY MESODERMAL DYSGENESIS OF THE CORNEA (PETER'S ANOMALY) IN TWO BROTHERSBOEL M; TIMMERMANS J; EMMERY L et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 51; NO 2; PP. 237-240; BIBL. 8 REF.Article

PIERRE-ROBIN ANOMALAD, MODERATE MENTAL RETARDATION AND DISTAL 4Q DELETIONFRYNS JP; TIMMERMANS J; HOEDEMAEKERS J et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 3; PP. 187-188; ABS. FRE; BIBL. 7 REF.Article

Familial infantile cortical hyperostosisEMMERY, L; TIMMERMANS, J; CHRISTENS, J et al.European journal of pediatrics. 1983, Vol 141, Num 1, pp 56-58, issn 0340-6199Article

A new type of autosomal recessive spondyloepiphyseal dysplasia tardaLEROY, J. G; LEROY, B. P; EMMERY, L. V et al.American journal of medical genetics. 2004, Vol 125A, Num 1, pp 49-56, issn 0148-7299, 8 p.Article

Trisomy (18q) and tetrasomy (18p) resulting from isochromosome formationKLECZKOWSKA, A; FRYNS, J. P; BUTTIENS, M et al.Clinical genetics. 1986, Vol 30, Num 6, pp 503-506, issn 0009-9163Article

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