au.\*:("GARDNER RJM")
Results 1 to 15 of 15
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A NEW ESTIMATE OF THE ACHONDROPLASIA MUTATION RATE.GARDNER RJM.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 11; NO 1; PP. 31-38; BIBL. 15 REF.Article
LOWE'S SYNDROME: IDENTIFICATION OF CARRIERS BY LENS EXAMINATION.GARDNER RJM; BROWN N.1976; J. MED. GENET.; G.B.; DA. 1976; VOL. 13; NO 6; PP. 449-454; BIBL. 9 REF.Article
DE NOVO TRANSLOCATION DOWN'S SYNDROME: RISK OF RECURRENCE OF DOWN'S SYNDROME = SYNDROME DE DOWN PAR TRANSLOCATION DE NOVO: RISQUE DE REAPPARITION DU SYNDROME DE DOWNGARDNER RJM; VEALE AMO.1974; CLIN. GENET.; DENM.; DA. 1974; VOL. 6; NO 3; PP. 160-164; BIBL. 20REF.Article
A FURTHER REPORT ON A KINDRED WITH CASES OF 4P TRISOMY AND MONOSOMYMORTIMER JG; CHEWINGS WE; GARDNER RJM et al.1980; HUM. HERED.; CHE; DA. 1980; VOL. 30; NO 1; PP. 58-61; BIBL. 6 REF.Article
A SYNDROME OF CONGENITAL THROMBOCYTOPENIA WITH MULTIPLE MALFORMATIONS AND NEUROLOGIC DYSFUNCTIONGARDNER RJM; MORRISON PS; ABBOTT GD et al.1983; JOURNAL OF PEDIATRICS; ISSN 0022-3476; USA; DA. 1983; VOL. 102; NO 4; PP. 600-602; BIBL. 14 REF.Article
MATERNAL HISTIDINAEMIA = HISTIDINEMIE MATERNELLELYON ICT; GARDNER RJM; VEALE AMO et al.1974; ARCH. DIS. CHILDH.; G.B.; DA. 1974; VOL. 49; NO 7; PP. 581-583; BIBL. 6REF.Article
GIEMSA BANDING IN THE T (13Q13Q) CARRIER MOTHER OF A TRANSLOCATION TRISOMY 13ABORTUS = COLORATION EN BANDES PAR LE GIEMSA CHEZ LA MERE CONDUCTRICE T (13Q13Q) D'UN AVORTON PORTEUR D'UNE TRISOMIE13 PAR TRANSLOCATIONPARSLOW MI; GARDNER RJM; VEALE AMO et al.1973; HUMANGENETIK; DTSCH.; DA. 1973; VOL. 18; NO 2; PP. 183-184; ABS. ALLEM.; BIBL. 4REF.Serial Issue
A MALFORMED BABY WITH TWO SEPARATE DE NOVO TRANSLOCATIONSCHEWINGS WE; COCKS TP; GARDNER RJM et al.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 1; PP. 70-71; BIBL. 6 REF.Article
A PROBABLE LINKAGE BETWEEN FAMILIAL PAGET'S DISEASE AND THE HLA LOCITILYARD MW; GARDNER RJM; MILLIGAN L et al.1982; AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE; ISSN 0004-8291; AUS; DA. 1982; VOL. 12; NO 5; PP. 498-500; BIBL. 8 REF.Article
ARE 1Q+ CHROMOSOMES HARMLESS. = LES CHROMOSOMES 1Q+ SONT-ILS INOFFENSIFS.GARDNER RJM; MCCREANOR HR; PARSLOW MI et al.1974; CLIN. GENET.; DENM.; DA. 1974; VOL. 6; NO 5; PP. 383-393; BIBL. 1P.1/2Article
THE FRAGILE X CHROMOSOME IN A LARGE INDIAN KINDREDGARDNER RJM; SMART RD; CORNELL JM et al.1983; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1983; VOL. 23; NO 4; PP. 311-317; BIBL. 14 REF.Article
XXXX SYNDROME: CASE REPORT, AND A NOTE ON GENETIC COUNSELLING AND FERTILITY = SYNDROME XXXX: OBSERVATION D'UN CAS ET NOTE SUR LE CONSEIL GENETIQUE ET LA FERTILITEGARDNER RJM; VEALE AMO; SANDS VE et al.1972; HUMANGENETIK; DTSCH.; DA. 1972; VOL. 17; NO 4; PP. 323-330; ABS. ALLEM.; BIBL. 1P.Serial Issue
DUPLICATION 8Q SYNDROME DUE TO FAMILIAL CHROMOSOME INS (10;8) (Q21;Q212Q22)BOWEN P; FITZGERALD PH; GARDNER RJM et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 4; PP. 635-646; BIBL. 25 REF.Article
AUTOSOMAL IMBALANCE WITH A NEAR-NORMAL PHENOTYPE: THE SMALL EFFECT OF TRISOMY FOR THE SHORT ARM OF CHROMOSOME 18GARDNER RJM; RUDD NL; STEVENS LJ et al.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6C; PP. 359-363; BIBL. 2 REF.Article
DIC (21;21) IN A DOWN'S SYNDROME CHILD WITH AN UNUSUAL CHROMOSOME 9 VARIANT IN THE MOTHERBERG JM; GARDNER HA; GARDNER RJM et al.1980; J. MED. GENET.; GBR; DA. 1980; VOL. 17; NO 2; PP. 144-148; BIBL. 9 REF.Article