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Items: 44

1.

Lowe oculocerebrorenal syndrome in a female with a balanced X;20 translocation: mapping of the X chromosome breakpoint.

Mueller OT, Hartsfield JK Jr, Gallardo LA, Essig YP, Miller KL, Papenhausen PR, Tedesco TA.

Am J Hum Genet. 1991 Oct;49(4):804-10.

2.

Cell line segregation in a 45,X/46,XY mosaic child with asymmetric leg growth.

Papenhausen PR, Mueller OT, Bercu B, Salazar J, Tedesco TA.

Clin Genet. 1991 Sep;40(3):237-41.

PMID:
1773540
3.

Florida newborn screening for galactosemia.

DeClue TJ, Malone JI, Tedesco TA.

J Fla Med Assoc. 1991 Jun;78(6):369-71.

PMID:
1831492
5.

Trisomy 3p23----pter and monosomy 11q23----qter in an infant with two translocation carrier parents.

Neu RL, Kousseff BG, Hardy DE, Essig YP, Miller KL, Jervis GA, Tedesco TA.

J Med Genet. 1988 Sep;25(9):631-3.

6.

Monosomy, trisomy, fragile sites, and rearrangements of chromosome no. 1 in a mentally retarded male with multiple congenital anomalies.

Neu RL, Kousseff BG, Madan S, Essig YP, Miller K, Tedesco TA.

Clin Genet. 1988 Feb;33(2):73-7.

PMID:
3359669
7.

Ultrasound identification of apparently normal male genitalia in a 46,X,+mar fetus.

Neu RL, O'Brien WF, Kousseff BG, Tedesco TA, Farmelo MJ, Essig YP, Miller KL, Nichols PM.

J Med Genet. 1987 Dec;24(12):782-3.

8.

Complex chromosome rearrangements and congenital anomalies.

Kousseff BG, Nichols P, Essig YP, Miller K, Weiss A, Tedesco TA.

Am J Med Genet. 1987 Apr;26(4):771-82.

PMID:
3591822
9.

Prenatal diagnosis in twin pregnancies.

Hager JM, Tedesco TA, Rattan PK, Knuppel RA, Miller KL, Farmelo MJ, Essig YP.

Birth Defects Orig Artic Ser. 1987;23(6):95-9. No abstract available.

PMID:
2449256
10.

Short stature in the genetic clinic.

Kousseff BG, Thomson-Meares J, Tedesco TA.

Prog Clin Biol Res. 1985;200:65-74. No abstract available.

PMID:
4080745
11.

Free amino acids in Citrullus vulgaris (watermelon)

Tedesco TA, Benford SA, Foster RC, Barness LA.

Pediatrics. 1984 Jun;73(6):879. No abstract available.

PMID:
6728593
12.

Counseling dilemmas in the prenatal diagnosis of 45,XO/46,XX mosaicism.

Hager J, Cortada X, Miller KL, Tedesco TA.

Birth Defects Orig Artic Ser. 1984;20(6):197-200. No abstract available.

PMID:
6535597
13.

Infant screening for galactosemia in Florida.

Tedesco TA.

J Fla Med Assoc. 1983 Sep;70(9):783-5. No abstract available.

PMID:
6631396
14.

Red cell sorbitol: an indicator of diabetic control.

Malone JI, Knox G, Benford S, Tedesco TA.

Diabetes. 1980 Nov;29(11):861-4.

PMID:
7429027
15.
16.

Temporal relationships between DNA metabolism and the growth-inhibitory response produced by dexamethasone in rat glioma cell cultures.

Grasso RJ, Tedesco TA, Wodzinski SF, Johnson CE.

In Vitro. 1978 Jul;14(7):625-30. No abstract available.

PMID:
669742
17.

Human erythrocyte galactose-1-phosphate uridylyltransferase. Evidence for a uridylyl-enzyme intermediate by kinetic and exchange reaction studies.

Markus HB, Wu JW, Boches FS, Tedesco TA, Mellman WJ, Kallen RG.

J Biol Chem. 1977 Aug 10;252(15):5363-9. No abstract available.

18.

The Philadelphia variant of galactokinase.

Tedesco TA, Miller KL, Rawnsley BE, Adams MC, Markus HB, Orkwiszewski KG, Mellman WJ.

Am J Hum Genet. 1977 May;29(3):240-7.

19.

Linkage relationship between the genes for thymidine kinase and galactokinase in different primates.

Orkwiszewski KG, Tedesco TA, Mellman WJ, Croce CM.

Somatic Cell Genet. 1976 Jan;2(1):21-6.

PMID:
195352
20.

Linkage of the genes for thymidine kinase and galactokinase in the Africian green monkey and the chimpanzee.

Orkwiszewski KG, Tedesco TA, Mellman WJ, Croce CM.

Birth Defects Orig Artic Ser. 1976;12(7):427-9. No abstract available.

PMID:
192374
21.

Linkage of the genes for thymidine kinase and galactokinase in the African green monkey and the chimpanzee.

Orkwiszewski KG, Tedesco TA, Mellman WJ, Croce CM.

Cytogenet Cell Genet. 1976;16(1-5):427-9. No abstract available.

PMID:
185024
22.

Galactose tolerance studies of individuals with reduced galactose pathway activity.

Mellman WJ, Rawnsley BE, Nichols CW, Needelman B, Mennuti MT, Malone J, Tedesco TA.

Am J Hum Genet. 1975 Nov;27(6):748-54.

23.

Human erythrocyte galactokinase and galactose-1-phosphate uridylyltransferase: a population survey.

Tedesco TA, Miller KL, Rawnsley BE, Mennuti MT, Spielman RS, Mellman WJ.

Am J Hum Genet. 1975 Nov;27(6):737-47.

24.

Letter: Localisation of human gene for galactose-1-phosphate-uridyltransferase.

Allerdice PW, Tedesco TA.

Lancet. 1975 Jul 5;2(7923):39. No abstract available.

PMID:
49636
25.

Assignment of the human gene for hexosaminidase B to chromosome 5.

Boedecker HJ, Mellman WJ, Tedesco TA, Croce CM.

Exp Cell Res. 1975 Jul;93(2):468-72. No abstract available.

PMID:
1171773
26.

The genetic defect in galactosemia.

Tedesco TA, Wu JW, Boches FS, Mellman WJ.

N Engl J Med. 1975 Apr 3;292(14):737-40. No abstract available.

PMID:
46587
27.

Galactosemia. Repository identification Nos. GM-52 and GM-53.

Mellman WJ, Tedesco TA, Greene AE, Coriell LL.

Cytogenet Cell Genet. 1975;15(3):198-9. No abstract available.

PMID:
1192846
28.

Studies on the molecular defect in galactosemia.

Tedesco TA.

UCLA Forum Med Sci. 1975;(18):467-77.

PMID:
173062
29.

Human galactose 1-phosphate uridylyltransferase. Absence of half-reaction activity of galactosemic proteins.

Wu JW, Tedesco TA, Kallen RG, Mellman WJ.

J Biol Chem. 1974 Nov 10;249(21):7038-9. No abstract available.

30.

Assignment of the human gene for galactokinase to chromosome 17.

Orkwiszewski KG, Tedesco TA, Croce CM.

Nature. 1974 Nov 1;252(5478):60-2. No abstract available.

PMID:
4427682
31.

Assignment of the human gene for hexose-1-phosphate uridylyltransferase to chromosome 3.

Tedesco TA, Diamond R, Orkwiszewski KG, Boedecker HJ, Croce CM.

Proc Natl Acad Sci U S A. 1974 Sep;71(9):3483-6.

32.

Normal pregnancy and childbirth in a galactosemic woman.

Tedesco TA, Morrow G 3rd, Mellman WJ.

J Pediatr. 1972 Dec;81(6):1159-61. No abstract available.

PMID:
4674573
34.

Galactokinase: evidence for a new racial polymorphism.

Tedesco TA, Bonow R, Miller K, Mellman WJ.

Science. 1972 Oct 13;178(4057):176-8.

PMID:
5076908
35.

Vertical column electrophoresis in sephadex G-200.

Tedesco TA, Bonow R, Mellman WJ.

Anal Biochem. 1972 Mar;46(1):173-80. No abstract available.

PMID:
5017655
36.

Galactosemia: evidence for a structural gene mutation.

Tedesco TA, Mellman WJ.

Science. 1971 May 14;172(3984):727-8.

PMID:
4995463
37.

Direct evidence of mutation at the locus for galactose-1-phosphate uridyl transferase.

Mellman WJ, Allen FH Jr, Baker L, Tedesco TA.

Pediatrics. 1970 Apr;45(4):672-6. No abstract available.

PMID:
5438169
39.

Inhibition of mammalian uridinediphosphoglucose 4-epimerase by the dithiothreitol-stimulated formation of NADH.

Tedesco TA, Mellman WJ.

Biochim Biophys Acta. 1969 Sep 30;191(1):144-54. No abstract available.

PMID:
4309907
40.

Argininosuccinate synthetase activity and citrulline metabolism in cells cultured from a citrullinemic subject.

Tedesco TA, Mellman WJ.

Proc Natl Acad Sci U S A. 1967 Mar;57(3):829-34. No abstract available.

41.

Desoxyribonucleic acid assay as a measure of cell number in preparations from monolayer cell cultures and blood leucocytes.

Tedesco TA, Mellman WJ.

Exp Cell Res. 1967 Jan;45(1):230-2. No abstract available.

PMID:
6022318
42.
43.

LEUCOCYTE ENZYMES IN DOWN'S SYNDROME.

MELLMAN WJ, OSKI FA, TEDESCO TA, MACIERA-COELHO A, HARRIS H.

Lancet. 1964 Sep 26;2(7361):674-5. No abstract available.

PMID:
14188913
44.

INDOLYLACROYL GLYCINE EXCRETION IN A FAMILY WITH MENTAL RETARDATION.

MELLMAN WJ, BARNESS LA, TEDESCO TA, BESSELMAN D.

Clin Chim Acta. 1963 Nov;8:843-7. No abstract available.

PMID:
14089554

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