Detection of Pseudomonas (Burkholderia) cepacia using PCR
Campbell, 3rd, P W, Phillips, 3rd, J A, Heidecker, G J, Krishnamani, M R, Zahorchak, R, Stull, T L
Published in Pediatric pulmonology (01.07.1995)
Published in Pediatric pulmonology (01.07.1995)
Get more information
Journal Article
A Novel Arginine Vasopressin-Neurophysin II Mutation Causes Autosomal Dominant Neurohypophyseal Diabetes insipidus and Morphologic Pituitary Changes
Skordis, Nicos, Patsalis, Philippos C., Hettinger, Joe A., Kontou, Maria, Herakleous, Eleni, Krishnamani, M.R.S., Phillips III, J.A.
Published in Hormone research (01.01.2000)
Published in Hormone research (01.01.2000)
Get full text
Journal Article
Screening for Growth Hormone (GH) Gene Deletions in Brazilian Patients with Isolated GH Deficiency
Osorio, M G F, Oliveira, S B, Estefan, V, Kamijo, T, Krishnamani, M R S, Cogan, J D, Phillips, J A, Mendonça, B B, Arnhold, I J P
Published in Pediatric research (01.03.1999)
Published in Pediatric research (01.03.1999)
Get full text
Journal Article
Heterogeneity in Clinical Manifestation of Autosomal Dominant Neurohypophyseal Diabetes Insipidus Caused by a Mutation Encoding Ala−1→Val in the Signal Peptide of the Arginine Vasopressin/Neurophysin II/Copeptin Precursor1
Repaske, David R, Medlej, Rita, Gültekin, Ebrû K, Krishnamani, M. R. S, Halaby, George, Findling, James W, Phillips, John A
Published in The journal of clinical endocrinology and metabolism (01.01.1997)
Published in The journal of clinical endocrinology and metabolism (01.01.1997)
Get full text
Journal Article
Heterogeneity in Clinical Manifestation of Autosomal Dominant Neurohypophyseal Diabetes Insipidus Caused by a Mutation Encoding Ala −1 →Val in the Signal Peptide of the Arginine Vasopressin/Neurophysin II/Copeptin Precursor 1
Repaske, David R., Medlej, Rita, Gültekin, Ebrû K., Krishnamani, M. R. S., Halaby, George, Findling, James W., Phillips, John A.
Published in The journal of clinical endocrinology and metabolism (01.01.1997)
Published in The journal of clinical endocrinology and metabolism (01.01.1997)
Get full text
Journal Article
Association of poor clinical status and heavy exposure to tobacco smoke in patients with cystic fibrosis who are homozygous for the F508 deletion
Campbell, Preston W., Parker, Robert A., Roberts, Barbara T., Krishnamani, M.R.S., Phillips, John A.
Published in The Journal of pediatrics (01.02.1992)
Published in The Journal of pediatrics (01.02.1992)
Get full text
Journal Article
Recurrent mutations in the vasopressin-neurophysin II gene cause autosomal dominant neurohypophyseal diabetes insipidus
REPASKE, D. R, SUMMAR, M. L, KRISHNAMANI, M. R. S, GÜLTEKIN, E. K, ARRIAZU, M. C, ROUBICEK, M. E, BLANCO, M, ISSAC, G. B, PHILLIPS, J. A
Published in The journal of clinical endocrinology and metabolism (01.06.1996)
Published in The journal of clinical endocrinology and metabolism (01.06.1996)
Get full text
Journal Article
Assignment of the gene (GLCLC) that encodes the heavy subunit of gamma-glutamylcysteine synthetase to human chromosome 6
Sierra-Rivera, E, Summar, M L, Dasouki, M, Krishnamani, M R, Phillips, J A, Freeman, M L
Published in Cytogenetics and cell genetics (01.01.1995)
Published in Cytogenetics and cell genetics (01.01.1995)
Get more information
Journal Article
Heterogeneity in clinical manifestation of autosomal dominant neurohypophyseal diabetes insipidus caused by a mutation encoding Ala-1→Val in the signal peptide of the arginine vasopressin/neurophysin II/copeptin precursor
REPASKE, D. R, MEDLEJ, R, GÜLTEKIN, E. K, KRISHNAMANI, M. R. S, HALABY, G, FINDLING, J. W, PHILLIPS, J. A
Published in The journal of clinical endocrinology and metabolism (1997)
Published in The journal of clinical endocrinology and metabolism (1997)
Get full text
Journal Article
Cystic Fibrosis in the Brazilian Population: DF508 Mutation and KM-19/XV-2C Haplotype Distribution
RASKIN, SALMO, PHILLIPS, JOHN A., KRISHNAMANI, M.R.S., VNENCAK-JONES, CINDY, PARKER, ROBERT A., ROZOV, TATIANA, CARDIERI, JOSELINA M., MAROSTICA, PAULO, ABREU, FERNANDO, GIUGLIANI, ROBERTO, REIS, FRANCISCO, ROSARIO, NELSON A., LUDWIG, NORBERTO, CULPI, LODÉRCIO
Published in Human biology (01.08.1997)
Get full text
Published in Human biology (01.08.1997)
Journal Article
Cystic fibrosis: Relationship between clinical status and F508 deletion
Campbell, Preston W., Phillips, John A., Krishnamani, M.R.S., Maness, Kimberly J., Hazinski, Thomas A.
Published in The Journal of pediatrics (01.02.1991)
Published in The Journal of pediatrics (01.02.1991)
Get full text
Journal Article
Regional Distribution of Cystic Fibrosis-Linked DNA Haplotypes in Brazil: Multicenter Study
RASKIN, SALMO, PHILIPS, JOHN A., KRISHNAMANI, M.R.S., VNENCAK-JONES, CINDY, PARKER, ROBERT A., DAWSON, ELLIOT, ROZOV, TATIANA, CARDIERI, JOSELINA M., MAROSTICA, PAULO, ABREU, FERNANDO, GIUGLIANI, ROBERTO, REIS, FRANCISCO, ROSARIO, NELSON A., LUDWIG, NORBERTO, CULPI, LODERCIO
Published in Human biology (01.02.1997)
Get full text
Published in Human biology (01.02.1997)
Journal Article
Physical and linkage mapping of human carbamyl phosphate synthetase I (CPS1) and reassignment from 2p to 2q35
Summar, M L, Dasouki, M J, Schofield, P J, Krishnamani, M R, Vnencak-Jones, C, Tuchman, M, Mao, J, Phillips, 3rd, J A
Published in Cytogenetics and cell genetics (1995)
Published in Cytogenetics and cell genetics (1995)
Get more information
Journal Article
Assignment of the human gene (GLCLR) that encodes the regulatory subunit of γ-glutamyl-cysteine synthetase to chromosome 1p21
SIERRA-RIVERA, E, DASOUKI, M, SUMMAR, M. L, KRISHNAMANI, M. R. S, MEREDITH, M, RAO, P. N, PHILLIPS, J. A, FREEMAN, M. L
Published in Cytogenetics and cell genetics (1996)
Get full text
Published in Cytogenetics and cell genetics (1996)
Conference Proceeding
Presumptive role of a pathovar of Xanthomonas in sudden death syndrome of soybean
Yopp, J, Krishnamani, M.R.S, Bozzola, J, Richardson, J, Myers, O, Klubek, B
Published in Microbios letters (1986)
Get more information
Published in Microbios letters (1986)
Journal Article