Pope Joan: a recognizable syndrome.

מאת New, M. I.
יצא לאור 1993

The Gordon Wilson Lecture. Congenital adrenal hyperplasia.

מאת New, M. I.
יצא לאור 1991

Aldosterone excretion in normal children and in children with adrenal hyperplasia.

מאת New, M I, Miller, B, Peterson, R E
יצא לאור 1966

Structure of human steroid 21-hydroxylase genes.

מאת White, P C, New, M I, Dupont, B
יצא לאור 1986

Cloning and expression of cDNA encoding a bovine adrenal cytochrome P-450 specific for steroid 21-hydroxylation.

מאת White, P C, New, M I, Dupont, B
יצא לאור 1984

HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation.

מאת White, P C, New, M I, Dupont, B
יצא לאור 1984

Characterization of frequent deletions causing steroid 21-hydroxylase deficiency.

מאת White, P C, Vitek, A, Dupont, B, New, M I
יצא לאור 1988

Frequent deletion and duplication of the steroid 21-hydroxylase genes.

מאת Werkmeister, J W, New, M I, Dupont, B, White, P C
יצא לאור 1986

Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency.

מאת Amor, M, Parker, K L, Globerman, H, New, M I, White, P C
יצא לאור 1988

Nonsense mutation causing steroid 21-hydroxylase deficiency.

מאת Globerman, H, Amor, M, Parker, K L, New, M I, White, P C
יצא לאור 1988

A mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan origin.

מאת White, P C, Dupont, J, New, M I, Leiberman, E, Hochberg, Z, Rösler, A
יצא לאור 1991

High frequency of nonclassical steroid 21-hydroxylase deficiency.

מאת Speiser, P W, Dupont, B, Rubinstein, P, Piazza, A, Kastelan, A, New, M I
יצא לאור 1985

A segregation and linkage study of classical and nonclassical 21-hydroxylase deficiency.

מאת Sherman, S L, Aston, C E, Morton, N E, Speiser, P W, New, M I
יצא לאור 1988

Genetic mapping of the 21-hydroxylase locus: estimation of small recombination frequencies.

מאת Aston, C E, Sherman, S L, Morton, N E, Speiser, P W, New, M I
יצא לאור 1988

Mutations in the CYP11B1 gene causing congenital adrenal hyperplasia and hypertension cluster in exons 6, 7, and 8.

מאת Curnow, K M, Slutsker, L, Vitek, J, Cole, T, Speiser, P W, New, M I, White, P C, Pascoe, L
יצא לאור 1993

Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2.

מאת Pascoe, L, Curnow, K M, Slutsker, L, Connell, J M, Speiser, P W, New, M I, White, P C
יצא לאור 1992

Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man.

מאת White, P C, Grossberger, D, Onufer, B J, Chaplin, D D, New, M I, Dupont, B, Strominger, J L
יצא לאור 1985

Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

מאת Speiser, P W, Dupont, J, Zhu, D, Serrat, J, Buegeleisen, M, Tusie-Luna, M T, Lesser, M, New, M I, White, P C
יצא לאור 1992

HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiency.

מאת Pollack, M S, Levine, L S, O'Neill, G J, Pang, S, Lorenzen, F, Kohn, B, Rondanini, G F, Chiumello, G, New, M I, Dupont, B
יצא לאור 1981

DAX1 mutations map to putative structural domains in a deduced three-dimensional model.

מאת Zhang, Y H, Guo, W, Wagner, R L, Huang, B L, McCabe, L, Vilain, E, Burris, T P, Anyane-Yeboa, K, Burghes, A H, Chitayat, D, Chudley, A E, Genel, M, Gertner, J M, Klingensmith, G J, Levine, S N, Nakamoto, J, New, M I, Pagon, R A, Pappas, J G, Quigley, C A, Rosenthal, I M, Baxter, J D, Fletterick, R J, McCabe, E R
יצא לאור 1998