IMINO ACID TRANSPORT IN HUMAN DIPLOID FIBROBLASTSREVSIN B; MORROW G III.1979; EXPER. CELL RES.; USA; DA. 1979; VOL. 119; NO 1; PP. 55-61; BIBL. 13 REF.Article

A DIAGNOSTIC APPROACH TO METABOLIC ACIDOSIS IN CHILDRENKAPPY MS; MORROW G III.1980; PEDIATRICS; USA; DA. 1980; VOL. 65; NO 2; PP. 351-356; BIBL. 23 REF.Article

A FAMILIAL SPINAL CORD DISORDER WITH HYPERGLYCINEMIA = UN SYNDROME MEDULLAIRE FAMILIAL AVEC HYPERGLYCINEMIEBANK WJ; MORROW G III.1972; ARCH. NEUROL.; U.S.A.; DA. 1972; VOL. 27; NO 2; PP. 136-144; BIBL. 32 REF.Serial Issue

GLYCINE TRANSPORT IN NORMAL AND NON-KETOTIC HYPERGLYCINEMIC HUMAN DIPLOID FIBROBLASTS.REVSIN B; MORROW G III.1976; EXPER. CELL RES.; U.S.A.; DA. 1976; VOL. 100; NO 1; PP. 95-103; BIBL. 24 REF.Article

STUDIES OF METHYLMALONYL-COENZYME A CARBONYLMUTASE ACTIVITY IN METHYLMALONIC ACIDEMIA.MORROW G III; LEBOWITZ J.1976; BIOCHEM. MED.; U.S.A.; DA. 1976; VOL. 15; NO 3; PP. 241-245; BIBL. 10 REF.Article

CONTINUOUS INSULIN INFUSION IN HYPERGLYCEMIC, VERY LOW BIRTH WEIGHT INFANTSVAUCHER YE; WALSON PD; MORROW G III et al.1982; J. PEDIATR. GASTROENTEROL. NUTR.; ISSN 504386; USA; DA. 1982; VOL. 1; NO 2; PP. 211-217; BIBL. 29 REF.Article

HISTIDINEMIA WITH FEATURES OF THE MARFAN SYNDROME = HISTIDINEMIE AVEC SIGNES D'UN SYNDROME DE MARFANSTEVENS R; CROSS HE; MORROW G III et al.1975; J. PEDIATR.; U.S.A.; DA. 1975; VOL. 86; NO 6; PP. 907-910; BIBL. 8REF.Article

NORMAL PREGNANCY AND CHILDBIRTH IN A GALACTOSEMIC WOMAN = GROSSESSE ET ACCOUCHEMENT NORMAUX CHEZ UNE FEMME GALACTOSEMIQUETEDESCO TA; MORROW G III; MELLMAN WJ et al.1972; J. PEDIATR.; U.S.A.; DA. 1972; VOL. 81; NO 6; PP. 1159-1161; BIBL. 6REF.Article

MATERNAL OBESITY, WEIGHT GAIN IN PREGNANCY, AND INFANT BIRTH WEIGHTHARRISON GG; UDALL JN; MORROW G III et al.1980; AMER. J. OBSTETR. GYNECOL.; USA; DA. 1980; VOL. 136; NO 3; PP. 411-412; BIBL. 2 REF.Article

IN VITRO RESPONSIVE METHYLMALONIC ACIDEMIA: A NEW VARIANT = ACIDEMIE METHYLMALONIQUE CURABLE IN VITRO: UNE NOUVELLE VARIANTEKAYE CI; MORROW G III; NADLER HL et al.1974; J. PEDIATR.; U.S.A.; DA. 1974; VOL. 85; NO 1; PP. 55-59; BIBL. 21REF.Article

A SIMPLE, RAPID METHOD FOR PRENATAL DETECTION OF DEFECTS IN PROPIONATE METABOLISM.MORROW G III; REVSIN B; MATHEWS C et al.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 10; NO 4; PP. 218-221; BIBL. 10 REF.Article

RETINOBLASTOMA IN A PATIENT WITH A 13QXP TRANSLOCATION.CROSS HE; HANSEN RC; MORROW G III et al.1977; AMER. J. OPHTHALMOL.; U.S.A.; DA. 1977; VOL. 84; NO 4; PP. 548-554; BIBL. 35 REF.Article

CALCIUM AND FAT ABSORPTION FROM INFANT FORMULAS WITH DIFFERENT FAT BLENDS = L'ABSORPTION DU CALCIUM ET DES GRAINES A PARTIR DE LAITS POUR NOURRISSONS CONTENANT DIFFERENTS MELANGES DE GRAISSESBARNES LA; MORROW G III; SILVERIO J et al.1974; PEDIATRIES; U.S.A.; DA. 1974; VOL. 54; NO 2; PP. 217-221; BIBL. 13REF.Article

Moped injuries in childrenWESTMAN, J. A; MORROW, G. III.Pediatrics (Evanston). 1984, Vol 74, Num 5, pp 820-822, issn 0031-4005, 1Article

DETECTION OF ERRORS IN METHYLMALONYL-COA METABOLISM BY USING AMNIOTIC FLUID.MORROW G III; REVSIN B; LEBOWITZ J et al.1977; CLIN. CHEM.; U.S.A.; DA. 1977; VOL. 23; NO 5; PP. 791-795; BIBL. 15 REF.Article

Hereditary fructose intoleranceLONG, W. W; PAWEL, B; MORROW, G. III et al.Archives of pediatrics & adolescent medicine. 1997, Vol 151, Num 11, pp 1165-1166, issn 1072-4710Article

A NEW VARIANT OF METHYLMALONIC ACIDEMIA-DEFECTIVE COENZYME-APOENZYME BINDING IN CULTURED FIBROBLASTS.MORROW G III; REVSIN B; CLARK R et al.1978; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1978; VOL. 85; NO 1; PP. 67-72; BIBL. 17 REF.Article

Atypical Menkes steely hair diseaseWESTMAN, J. A; RICHARDSON, D. C; RENNERT, O. M et al.American journal of medical genetics. 1988, Vol 30, Num 3, pp 853-858, issn 0148-7299Article

Clinical application of DNA analysis in a family with OTC deficiencyMCCLEAD, R. E. JR; ROZEN, R; FOX, J et al.American journal of medical genetics. 1986, Vol 25, Num 3, pp 513-518, issn 0148-7299Article