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au.\*:("HARROD MJ")

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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

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

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