A. Kulharya

发表

Acute leukemia with PICALM-MLLT10 fusion gene: diagnostic and treatment struggle.

C. Mecucci, V. Pierini, C. Ustun, 2010, Cancer genetics and cytogenetics.

Cutaneous sclerosing extramedullary hematopoietic tumor in chronic myelogenous leukemia

J. Lane, A. Kulharya, A. Walker, 2002, Journal of cutaneous pathology.

Long‐term follow‐up and analysis of monozygotic twins concordant for 45,X/46,XY peripheral blood karyotype but discordant for phenotypic sex

P. McDonough, L. Layman, R. Reindollar, 2007, American journal of medical genetics. Part A.

Involvement of p54(nrb), a PSF partner protein, in DNA double-strand break repair and radioresistance

W. Kuhne, Kyungsoo Ha, W. Dynan, 2009, Nucleic acids research.

Relapsed acute myelogenous leukemia occurring after 18 years with recurrent novel chromosomal abnormality t(18;22)(q23;q11.2).

R. Bollag, A. Jillella, A. Kulharya, 2007, Cancer genetics and cytogenetics.

Fine mapping of breakpoints in two unrelated patients with rare overlapping interstitial deletions of 9q with mild dysmorphic features

B. Levy, G. Velagaleti, D. Flannery, 2008, American journal of medical genetics. Part A.

Near-tetraploidy clone can evolve from a hyperdiploidy clone and cause resistance to lenalidomide and bortezomib in a multiple myeloma patient.

Ji Yuan, C. Ustun, A. Kulharya, 2010, Leukemia research.

Packed red cell transfusion does not compromise chromosome analysis in newborns

D. Flannery, B. Salbert, L. Cook, 2001, Genetics in Medicine.

Interstitial deletions 4q21.1q25 and 4q25q27: phenotypic variability and relation to Rieger anomaly.

Golder N Wilson, V. Tonk, N. Schneider, 1995, American journal of medical genetics.

Kenny-Caffey syndrome and microorchidism.

K. Kovacs, W. Cleveland, M. Eidson, 1998, American journal of medical genetics.

Phenotypic spectrum of 45,X/46,XY males with a ring Y chromosome and bilaterally descended testes.

Paul G McDonough, P. McDonough, L. Layman, 2009, Fertility and sterility.

Radiation therapy depletes extrachromosomally amplified drug resistance genes and oncogenes from tumor cells via micronuclear capture of episomes and double minute chromosomes.

M. Dohn, P. Schoenlein, Ana Sanchez, 2003, International journal of radiation oncology, biology, physics.

Clinical and molecular characterization of a large sample of patients with hypogonadotropic hypogonadism.

D. Bick, L. Layman, R. Podolsky, 2006, Fertility and sterility.

WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.

Cheol‐Hee Kim, M. Tekin, T. Nagase, 2010, American journal of human genetics.

Maternal complex chromosome rearrangement ascertained through a del (13)(q12.1q14.1) detected in her mildly affected daughter.

V. Tonk, A. Kulharya, M. Drummond-Borg, 2002, American journal of medical genetics.

Prenatal diagnosis of a trisomy 17p derived from a de novo non‐mosaic satellited marker

D. Flannery, A. Kulharya, L. Keppen, 1998, Clinical genetics.

Constitutional del(19)(q12q13.1) in a three-year-old girl with severe phenotypic abnormalities affecting multiple organ systems.

R. Michaelis, A. Kulharya, H. Taylor, 1998, American journal of medical genetics.

Mild phenotypic effects of a de novo deletion Xpter-->Xp22.3 and duplication 3pter-->3p23.

J. Belmont, M. Kukolich, A. Kulharya, 1995, American journal of medical genetics.

Prenatal diagnosis of a de novo trisomy 6q22.2→6qter and monosomy lpter→1p36.3. Case report with a 2‐year follow‐up and a brief review of other prenatal cases of partial trisomy 6q

M. Huslig, M. Kukolich, M. Carlin, 1997, Clinical genetics.

Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients.

E. Thorland, N. Lindor, D. Dawson, 2003, American journal of human genetics.

Trisomy 22: no longer an enigma.

S. Jalal, M. Kukolich, A. Kulharya, 1989, American journal of medical genetics.

Unusual mosaic karyotype resulting from adjacent 1 segregation of t(11;22): importance of performing skin fibroblast karyotype in patients with unexplained multiple congenital anomalies.

D. Flannery, A. Kulharya, Carolyn Lovell, 2002, American journal of medical genetics.

Mosaic Tetrasomy 13q and Phylloid Hypomelanosis: A Case Report and Review of the Literature

D. Sheehan, L. Davis, A. Kulharya, 2015, Pediatric dermatology.

Three cases of dup(10p)/del(10q) syndrome resulting from maternal pericentric inversion.

Golder N Wilson, N. Schneider, G. Wilson, 1993, American journal of medical genetics.

Erratum: Prenatal diagnosis of a de novo trisomy 6q22.2→6qter and monosomy 1pter→1p36.3. Case report with a 2-year follow-up and a brief review of other prenatal cases of partial trisomy 6q (Clinical Genetics (1997) 51 (115-117))

M. Huslig, M. Kukolich, M. Carlin, 1997 .

Exclusion of SIX6 hemizygosity in a child with anophthalmia, panhypopituitarism and renal failure.

R. Figueroa, M. Rauchman, J. Hanna, 2001, American journal of medical genetics.

A rare case of complete monosomy 21 with multiple osseous, cardiac, and vascular anomalies

Arie Franco, M. Shah, J. Bhatia, 2010 .

Granular Acute Lymphoblastic Leukemia in Adults: Report of a Case and Review of the Literature

K. L. Satya-Prakash, A. Kulharya, F. Mazzella, 2006, Southern medical journal.

Complete monosomy 21 confirmed by FISH and array‐CGH

V. Tonk, D. Flannery, A. Kulharya, 2012, American journal of medical genetics. Part A.

Genotoxicity associated with hydroxyurea exposure in infants with sickle cell anemia: Results from the BABY‐HUG phase III clinical trial

R. Ware, B. Thompson, T. Howard, 2012, Pediatric blood & cancer.

Isolated trisomy 10 in an infant with acute myeloid leukemia: a case report and review of literature.

Ji Yuan, P. Ramalingam, E. Manaloor, 2010, International journal of clinical and experimental pathology.

Near-tetraploidy clone can evolve from a hyperdiploidy clone and cause resistance to lenalidomide and bortezomib in a multiple myeloma patient.

Ji Yuan, C. Ustun, A. Kulharya, 2010, Leukemia research : a Forum for Studies on Leukemia and Normal Hemopoiesis.