QUANTITATION OF HEMOGLOBIN A₂ IN ALPHA THALASSEMIA TRAIT BY MICROCOLUMN CHROMATOGRAPHYMCCORMACK MK.1980; CLIN. CHIM. ACTA; NLD; DA. 1980; VOL. 105; NO 3; PP. 387-391; BIBL. 16 REF.Article

IMPROVED VISUALIZATION OF FETAL HEMOGLOBIN-CONTAINING CELLS USING NOMARSHI OPTICSMCCORMACK MK; TOKE D.1983; CLINICAL BIOCHEMISTRY; ISSN 0009-9120; CAN; DA. 1983; VOL. 16; NO 3; PP. 188-190; BIBL. 22 REF.Article

ALTERED RED OSMOTIC FRAGILITY IN HUNTINGTON DISEASE (HD)MCCORMACK MK; ULLMAN J; LAZZARINI A et al.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 11; NO 1; PP. 53-59; BIBL. 19 REF.Article

DELAYED SKELETAL MATURATION IN SICKLE CELL TRAIT = RETARD DE MATURATION SQUELETTIQUE DANS LE TRAIT DREPANOCYTAIREMCCORMACK MK; KATZ SH; DICKER L et al.1975; J. PEDIATR.; U.S.A.; DA. 1975; VOL. 87; NO 3; PP. 489-490; BIBL. 7 REF.Article

RISK FACTORS ASSOCIATED WITH NEURAL TUBE DEFECTSMCCORMACK MK; BRESLIN N; COPPOLA MCCORMACK PJ et al.1980; CLIN. GENET.; DNK; DA. 1980; VOL. 17; NO 6; PP. 394-402; BIBL. 23 REF.Article

A NEW KINDRED WITH HEMOGLOBIN MALMOE (BETA 97->GLN).MCCORMACK MK; ZAK SJ; GELLER GR et al.1976; J. PEDIATR.; U.S.A.; DA. 1976; VOL. 88; NO 6; PP. 1061-1063; BIBL. 4 REF.Article

IDENTIFICATION OF THE ASYMMETRIC HYBRID OF HUMAN OXY HEMOGLOBINS A AND S (ALPHA ₂BETA ^ABETA ^S) AT 4^OC BY CELLULOSE ACETATE ELECTROPHORESISMCCORMACK MK; WESTBROOK TG; PAULL RM et al.1981; HEMOGLOBIN; USA; DA. 1981; VOL. 5; NO 3; PP. 251-256; BIBL. 22 REF.Article

AUTOSOMAL-DOMINANT INHERITANCE OF DISTAL ARTHROGRYPOSISMCCORMACK MK; COPPOLA MCCORMACK PJ; MING LIANG LEE et al.1980; AMER. J. MED. GENET.; USA; DA. 1980; VOL. 6; NO 2; PP. 163-169; BIBL. 5 REF.Article

COMPLEX ALPHA -THALASSEMIA-LIKE SYNDROME: A CAUSE OF NEONATAL NORMOBLASTEMIA.MCCORMACK MK; GELLER GR; ZAK S et al.1976; J. PEDIATR.; U.S.A.; DA. 1976; VOL. 89; NO 3; PP. 446-451; BIBL. 12 REF.Article

A COMPARISON OF THE PHYSICAL AND INTELLECTUAL DEVELOPMENT OF BLACK CHILDREN WITH AND WITHOUT SICKLE-CELL TRAIT = UNE COMPARAISON ENTRE LE DEVELOPPEMENT PHYSIQUE ET INTELLECTUEL DES ENFANTS NOIRS PORTEURS OU NON DU TRAIT DREPANOCYTAIREMCCORMACK MK; SCARR SALAPATEK S; POLESKY H et al.1975; PEDIATRICS; U.S.A.; DA. 1975; VOL. 56; NO 6; PP. 1021-1025; BIBL. 37 REF.Article

GROWTH PATTERNS OF CHILDREN WITH SICKLE-CELL DISEASE.MCCORMACK MK; DICKER L; KATZ SH et al.1976; HUM. BIOL.; U.S.A.; DA. 1976; VOL. 48; NO 3; PP. 429-437; BIBL. 1 P.Article

ATTITUDES REGARDING UTILIZATION OF ARTIFICIAL INSEMINATION BY DONOR IN HUNTINGTON DISEASEMCCORMACK MK; LEIBLUM S; LAZZARINI A et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 1; PP. 5-13; BIBL. 19 REF.Article

BIS-(N-MALEIMIDOMETHYL) ETHER: AN ANTISICKLING REAGENT.ZAK SJ; GELLER GR; FINKEL B et al.1975; PROC. NATION. ACAD. SCI. U.S.A.; U.S.A.; DA. 1975; VOL. 72; NO 10; PP. 4153-4156; BIBL. 9 REF.Article