I. Gadi

发表

Glucose metabolism and insulin secretion in a patient with ABCC8 mutation and Fanconi–Bickel syndrome caused by maternal isodisomy of chromosome 3

C. Stanley, P. Galvin-Parton, R. Santer, 2007, Clinical genetics.

High recombination between two physically close human basement membrane collagen genes at the distal end of chromosome 13q.

E. Wijsman, L. Cavalli-Sforza, J. Hebert, 1988, Proceedings of the National Academy of Sciences of the United States of America.

UPD detection using homozygosity profiling with a SNP genotyping microarray

S. Schwartz, P. Papenhausen, J. Tepperberg, 2011, American journal of medical genetics. Part A.

A prenatal diagnosis of mosaic trisomy 5 reveals a postnatal complete uniparental disomy of chromosome 5 with multiple congenital anomalies

B. Helm, S. S. Schrier Vergano, I. Gadi, 2017, American journal of medical genetics. Part A.

Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotype

S. Schwartz, A. Hamosh, P. Papenhausen, 2013, American journal of medical genetics. Part A.

Genetic analysis of tumorigenesis. XXXI: Retention of short arm of chromosome 3 in suppressed CHEF cell hybrids containing c-Ha-ras (EJ) gene

R. Craig, R. Sager, I. Gadi, 1988, Somatic cell and molecular genetics.

Genetic analysis of tumerigenesis: XVI. Chromosome changes in azacytidine- and insulin-induced tumorigenesis

R. Sager, J. J. Harrison, I. Gadi, 1984, Somatic cell and molecular genetics.

Genetic analysis of tumorigenesis: X. Chromosome studies of transformed mutants and tumor-derived CHEF/18 cells

R. Sager, R. Kitchin, B. Smith, 1982, Somatic cell genetics.

The genes coding for human pro alpha 1(IV) collagen and pro alpha 2(IV) collagen are both located at the end of the long arm of chromosome 13.

J. Mackenzie, M. Condon, S. Toth-Fejel, 1988, American journal of human genetics.

Human and primate monoclonal antibodies for in vivo therapy.

P. Ehrlich, Z. A. Moustafa, J. Justice, 1988, Clinical chemistry.

Spontaneous mutation rates of tumorigenic and nontumorigenic Chinese hamster embryo fibroblast cell lines.

D. Kaden, L. Bardwell, R. Gelman, 1989, Cancer research.

Blastocyst implantation depends on maternal expression of leukaemia inhibitory factor

C. Stewart, H. Bhatt, Frank Köntgen, 1992, Nature.

Highly Purified Pheophorbide A As A Photosensitizer In Human Bladder Carcinoma In Vitro

Alvin B. Segelman, I. Kathleen Hagen, Simon A. Chernomorsky, 1988, Other Conferences.

Supernumerary chromosomes in Bandicota indica nemorivaga and a female individual with XX/XO mosaicism

R. Raman, I. Gadi, T. Sharma, 1982, Genetica.

Distribution of silver-stained nucleolus-organizing regions in the chromosomes of the Equidae

O. Ryder, I. Gadi, 1983, Genetica.

Ovotesticular disorder of sexual development (true hermaphroditism).

J. Tepperberg, L. Palmer, L. Mehta, 2009, Urology.

Stem cells from primordial germ cells can reenter the germ line.

C. Stewart, H. Bhatt, I. Gadi, 1994, Developmental biology.

Androgenetic mouse embryonic stem cells are pluripotent and cause skeletal defects in chimeras: Implications for genetic imprinting

C. Stewart, J. Mann, S. Abbondanzo, 1990, Cell.

Azacytidine-induced tumorigenesis of CHEF/18 cells: correlated DNA methylation and chromosome changes.

M. Raffeld, A. Anisowicz, R. Sager, 1983, Proceedings of the National Academy of Sciences of the United States of America.

Derivation of embryonic stem cell lines.

C. Stewart, S. Abbondanzo, S J Abbondanzo, 1993, Methods in enzymology.

Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay

S. Schwartz, P. Papenhausen, A. Carroll, 2011, Human Genetics.

Chromosomal Microarray Analysis in Clinical Evaluation of Neurodevelopmental Disorders-Reporting a Novel Deletion of SETDB1 and Illustration of Counseling Challenge

Xiu Xu, C. Rehder, Heather Labreche, 2016, Pediatric Research.

Phenotypic heterogeneity in a family with a small atypical microduplication of chromosome 22q11.2 involving TBX1.

L. Edelmann, J. Weisfeld-Adams, L. Mehta, 2012, European journal of medical genetics.

Cytogenetic relationships inRattus, Cremnomys, Millardia, Nesokia andBandicota (Rodentia: Muridae)

T. Sharma, I. Gadi, 2004, Genetica.

Mosaic paternal genome‐wide uniparental isodisomy with down syndrome

P. Atwal, Cathy Angell, R. Wallerstein, 2015, American journal of medical genetics. Part A.

Maternal Uniparental Isodisomy Causing Autosomal Recessive GM1 Gangliosidosis: A Clinical Report

A. Vanderver, Johanna L Schmidt, A. Pizzino, 2014, Journal of Genetic Counseling.

T. Sharma, R. Raman, I. Gadi, 2004, Genetica.

origenesis in Chinese hamster

C. Lau, R. Sager, I. Gadi, 2016 .

Partial trisomy 19p13.3 and partial monosomy 1p36.3: Clinical report and a literature review

J. Savla, E. Garrow, Bgee Kunjumon, 2009, American journal of medical genetics. Part A.

Homograft valve durability: Host or donor influence?

J. Mackenzie, A. Spotnitz, J. Gu, 2005, Heart and Vessels.

Gene amplification: an example of accelerated evolution in tumorigenic cells.

R. Sager, L. Stephens, C. Grabowy, 1985, Proceedings of the National Academy of Sciences of the United States of America.

The Genes Coding for Human Pro o I (IV) Collagen and Pro a2(IV) Collagen Are Both Located at the End of the Long Arm of Chromosome 13

J. Mackenzie, Markku, M. Litt, 2006 .

Gene amplification: an example of accelerated evolution in tumorigenic cells.

R. Sager, L. Stephens, C. Grabowy, 1985, Proceedings of the National Academy of Sciences of the United States of America.

Constitutive heterochromatin variation in two species of rattus with apparently similar karyotypes

T. Sharma, I. Gadi, 1977, Genetica.

UPD detection using homozygosity profiling with a SNP genotyping microarray

S. Schwartz, P. Papenhausen, J. Tepperberg, 2011, American journal of medical genetics. Part A.