au.\*:("HARROD MJ")
Results 1 to 7 of 7
Selection :
A SYNDROME OF CRANIOFACIAL, DIGITAL, AND GENITAL ANOMALIES.HARROD MJ; KEELE DK; HOWARD J JR et al.1977; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1977; VOL. 13; NO 3B; PP. 111-115; BIBL. 1 REF.Article
LINKAGE INVESTIGATION OF A LARGE FAMILY WITH REIFENSTEIN'S SYNDROME = EXAMEN DES LIAISONS DANS UNE FAMILLE NOMBREUSE CONDUCTRICE DU SYNDROME DE REIFENSTEINOTT J; GOLDSTEIN JL; HARROD MJ et al.1975; CLIN. GENET.; DENM.; DA. 1975; VOL. 7; NO 4; PP. 342-344; BIBL. 4 REF.Article
RING 17 CHROMOSOME DETECTED BY AMNIOCENTESIS = CHROMOSOME 17 ANNULAIRE DECOUVERT PAR AMNIOCENTESEWEINBERG AG; BAIR JL; HARROD MJ et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 28; NO 3; PP. 269-272; BIBL. 10 REF.Article
CONGENITAL ABSENCE OF THE VAGINA. THE MAYER-ROKITANSKY-KUSTER-HAUSER SYNDROME.GRIFFIN JE; EDWARDS C; MADDEN JD et al.1976; ANN. INTERN. MED.; U.S.A.; DA. 1976; VOL. 85; NO 2; PP. 224-236; BIBL. 2 P.Article
FAMILIAL ABSORPTIVE HYPERCALCIURIA IN A LARGE KINDREDPAK CYC; MCGUIRE J; PETERSON R et al.1981; J. UROL.; ISSN 0022-5347; USA; DA. 1981; VOL. 126; NO 6; PP. 717-719; BIBL. 15 REF.Article
A-L-IDURONIDASE DEFICIENCY AND POSSIBLE HURLER-SCHEIE GENETIC COMPOUND.WINTERS PR; HARROD MJ; MOLENICH HEETRED SA et al.1976; NEUROLOGY; U.S.A.; DA. 1976; VOL. 26; NO 11; PP. 1003-1007; BIBL. 10 REF.Article
A CUTANEOUS MARKER IN THE HUNTER SYNDROME. A REPORT OF FOUR CASES.PRYSTOWSKY SD; MAUMENEE IH; FREEMAN RG et al.1977; ARCH. DERMATOL.; U.S.A.; DA. 1977; VOL. 113; NO 5; PP. 602-605; BIBL. 15 REF.Article