EXTENSIVE PRESENTATION OF VERRUCA PLANA IN A HEALTHY INDIVIDUAL

par Pavithra, S, Mallya, H, Pai, G S
Publié 2011

Cardiofaciocutaneous Syndrome: A Rare Entity

par Pavithra, S, Mallya, H, Pai, G S
Publié 2012

The QT interval in atrial fibrillation.

par Pai, G R, Rawles, J M
Publié 1989

A case of respiratory sinus arrhythmia and vasovagal attacks: use of cosinor analysis for diagnosis and for monitoring treatment.

par Pai, G R, Rawles, J M
Publié 1987

Pericardial effusion after open heart surgery.

par D'Cruz, I A, Pai, G M
Publié 1991

Mutational analysis of the biglycan gene excludes it as a candidate for X-linked dominant chondrodysplasia punctata, dyskeratosis congenita, and incontinentia pigmenti.

par Das, S., Metzenberg, A., Pai, G. S., Gitschier, J.
Publié 1994

D-PENICILLAMINE INDUCED ELASTOSIS PERFORANS SERPIGINOSA MIMICKING ACNE KELOIDALIS NUCHAE

par Pavithra, S, Rao, Sanath, Vishal, B, Pai, G S
Publié 2011

VERRUCOUS HEMANGIOMA OR ANGIOKERATOMA? A MISSED DIAGNOSIS

par Pavithra, S, Mallya, H, Kini, H, Pai, G S
Publié 2011

NEVUS COMEDONICUS SYNDROME

par Pavithra, S, Pai, Harsha, Mallya, H, Pai, G S
Publié 2011

Salivary protein concentration, flow rate, buffer capacity and pH estimation: A comparative study among young and elderly subjects, both normal and with gingivitis and periodontiti...

par Shaila, Mulki, Pai, G. Prakash, Shetty, Pushparaj
Publié 2013

Absence of constitutive heterochromatin in a partially identified supernumerary marker chromosome.

par Pai, G S, Thomas, G H, Benke, P J
Publié 1981

Enhanced G2 chromatid radiosensitivity in dyskeratosis congenita fibroblasts.

par DeBauche, D M, Pai, G S, Stanley, W S
Publié 1990

One thousand heart attacks in Grampian: the place of cardiopulmonary resuscitation in general practice.

par Pai, G R, Haites, N E, Rawles, J M
Publié 1987

Autism Spectrum Disorder, Klinefelter Syndrome, and Chromosome 3p21.31 Duplication: A Case Report

par Stuart, Scott W., King, Casey H., Pai, G. Shashidar
Publié 2007

The origin and behavior of two isodicentric bisatellited chromosomes.

par Van Dyke, D L, Weiss, L, Logan, M, Pai, G S
Publié 1977

Molecular evidence that the p55 gene is not responsible for either of two Xq28-linked disorders: Emery-Dreifuss muscular dystrophy and dyskeratosis congenita.

par Metzenberg, A. B., Pan, Y., Das, S., Pai, G. S., Gitschier, J.
Publié 1994

Localization of loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase and biochemical evidence of nonrandom X chromosome expression from studies of...

par Pai, G S, Sprenkle, J A, Do, T T, Mareni, C E, Migeon, B R
Publié 1980

Xp pseudoautosomal gene haploinsufficiency and linear growth deficiency in three girls with chromosome Xp22;Yq11 translocation.

par Joseph, M, Cantú, E S, Pai, G S, Willi, S M, Papenhausen, P R, Weiss, L
Publié 1996

Preparation and Characterisation of Fluconazole Vaginal Films for the Treatment of Vaginal Candidiasis

par Kumar, L., Reddy, M. S., Shirodkar, R. K., Pai, G. K., Krishna, V. T., Verma, R.
Publié 2013

[(13)C]‐galactose breath test in a patient with galactokinase deficiency and spastic diparesis

par Ficicioglu, Can, Demirbas, Didem, Derks, Britt, Pai, G. Shashidhar, Timson, David J., Rubio‐Gozalbo, Maria Estela, Berry, Gerard T.
Publié dans JIMD Rep (2021)