The fetus as patient.

Por Mahoney, M J
Publicado em 1989

Letter: On abortion and neonatal mortality.

Por Mahoney, M J
Publicado em 1975

Letter: On "the right to choose abortion", an editorial.

Por Mahoney, M J
Publicado em 1975

Study of factors causing excess protoporphyrin accumulation in cultured skin fibroblasts from patients with protoporphyria.

Por Bloomer, J R, Brenner, D A, Mahoney, M J
Publicado em 1977

Heme synthetase deficiency in human protoporphyria. Demonstration of the defect in liver and cultured skin fibroblasts.

Por Bonkowsky, H L, Bloomer, J R, Ebert, P S, Mahoney, M J
Publicado em 1975

DNA analysis of first-trimester chorionic villous biopsies: test for maternal contamination.

Por de Martinville, B, Blakemore, K J, Mahoney, M J, Francke, U
Publicado em 1984

Methylmalonicacidemia: biochemical heterogeneity in defects of 5'-deoxyadenosylcobalamin synthesis.

Por Mahoney, M J, Hart, A C, Steen, V D, Rosenberg, L E
Publicado em 1975

Genetic complementation in heterokaryons of human fibroblasts defective in cobalamin metabolism.

Por Gravel, R A, Mahoney, M J, Ruddle, F H, Rosenberg, L E
Publicado em 1975

Deletion (12)(q15q21.2).

Por Watson, M S, McAllister-Barton, L, Mahoney, M J, Breg, W R
Publicado em 1989

Autosomal recessive inheritance of human mitochondrial carbamyl phosphate synthetase deficiency.

Por McReynolds, J W, Crowley, B, Mahoney, M J, Rosenberg, L E
Publicado em 1981

A method of processing first-trimester chorionic villous biopsies for cytogenetic analysis.

Por Blakemore, K J, Watson, M S, Samuelson, J, Breg, W R, Mahoney, M J
Publicado em 1984

Unusual inheritance of primary ciliary dyskinesia (Kartagener's syndrome).

Por Narayan, D, Krishnan, S N, Upender, M, Ravikumar, T S, Mahoney, M J, Dolan, T F, Teebi, A S, Haddad, G G
Publicado em 1994

First-trimester prenatal diagnosis of Tay-Sachs disease.

Por Grabowski, G A, Kruse, J R, Goldberg, J D, Chockkalingam, K, Gordon, R E, Blakemore, K J, Mahoney, M J, Desnick, R J
Publicado em 1984

A New Subtype of Brachydactyly Type B Caused by Point Mutations in the Bone Morphogenetic Protein Antagonist NOGGIN

Por Lehmann, K. , Seemann, P. , Silan, F. , Goecke, T. O. , Irgang, S. , Kjaer, K. W. , Kjaergaard, S. , Mahoney, M. J. , Morlot, S. , Reissner, C. , Kerr, B. , Wilkie, A. O. M. , Mundlos, S. 
Publicado em 2007