V. Petrovic

发表

The application of RNA sequencing for the diagnosis and genomic classification of pediatric acute lymphoblastic leukemia.

Anthony D. K. Hawkins, A. Oshlack, P. Ekert, 2020, Blood advances.

Expansion of the CGG repeat in fragile X in the FMR1 gene depends on the sex of the offspring.

D. Loesch, R. Huggins, H. Slater, 1995, American journal of human genetics.

Complex CGH alterations on chromosome arm 8p at candidate tumor suppressor gene loci in breast cancer cell lines.

M. de Silva, D. Venter, S. Ramus, 2005, Cancer genetics and cytogenetics.

High incidence of H-ras oncogene mutations in squamous cell carcinoma of lip vermilion.

Z. Nikolic, B. Dimitrijević, J. Milašin, 1994, Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology.

Two forms of ring 13 in a child with rhabdomyosarcoma.

L. Voullaire, V. Petrovic, P. Campbell, 1991, American journal of medical genetics.

Use of ubiquitous, highly heterozygous copy number variants and digital droplet polymerase chain reaction to monitor chimerism after allogeneic haematopoietic stem cell transplantation.

D. Bruno, H. Slater, R. Conyers, 2017, Experimental hematology.

PRENATAL DIAGNOSIS OF PRADER–WILLI SYNDROME USING PW71 METHYLATION ANALYSIS—UNIPARENTAL DISOMY AND THE SIGNIFICANCE OF RESIDUAL TRISOMY 15

M. Pertile, H. Slater, T. Burgess, 1997, Prenatal diagnosis.

A functional marker centromere with no detectable alpha-satellite, satellite III, or CENP-B protein: activation of a latent centromere?

L. Voullaire, K. Choo, H. Slater, 1993, American journal of human genetics.

The importance of further cytogenetic and molecular investigation of acrocentric variants: justification by presentation of a case [t(8;14)(q24;p11)]

M. Leversha, D. Danks, L. Voullaire, 1991, Human Genetics.

A new variant of chromosome 3 with unusual staining properties.

V. Petrovic, 1988, Journal of medical genetics.

Targeted therapy and disease monitoring in CNTRL‐FGFR1‐driven leukaemia

A. Oshlack, P. Ekert, I. Majewski, 2019, Pediatric blood & cancer.

Comparing saliva and blood for the detection of mosaic genomic abnormalities that cause syndromic intellectual disability

I. Scheffer, Anand Vasudevan, K. Oliver, 2022, European Journal of Human Genetics.

Abstracts of the 37th American Cytogenetics Conference

C. Steinlein, M. Schmid, S. Antonarakis, 2002, Cytogenetic and Genome Research.

Molecular mapping of the putative gonadoblastoma locus on the Y chromosome

D. Page, A. de la Chapelle, P. Peltomäki, 1995, Genes, chromosomes & cancer.

Minute Y chromosome derived marker in a child with gonadoblastoma: cytogenetic and DNA studies.

L. Voullaire, M. Schmidt, V. Petrovic, 1992, Journal of medical genetics.

H-ras gene mutations in salivary gland pleomorphic adenomas.

J. Milašin, V. Petrovic, N. Pujic, 1993, International journal of oral and maxillofacial surgery.

Loss of TOP3B leads to increased R-loop formation and genome instability

D. Hudson, P. Kalitsis, M. Wallis, 2019, Open Biology.

“Reduction” of CGG trinucleotide expansion from mother to offspring in seven fragile‐X families

D. Loesch, D. Francis, H. Slater, 1997, Clinical genetics.

Directly inherited partial trisomy of chromosome 6p identified in a father and daughter by chromosome microdissection

M. Delatycki, L. Voullaire, D. Francis, 1999, Journal of medical genetics.

Low grade fibromyxoid sarcoma: problems in the diagnosis and management of a malignant tumour with bland histological appearance

C. Chow, I. Torode, Xiangru Wu, 2009, Pathology.

X chromosome inactivation in fibroblasts of mentally retarded female carriers of the fragile site Xq27.3: application of the probe M27 beta to evaluate X inactivation status.

M. Leversha, L. Voullaire, P. Kalitsis, 1991, American journal of medical genetics.

Cytogenetic and DNA analysis of two neuroectodermal tumors without a simple t(11;22).

L. Voullaire, H. Slater, G. Kannourakis, 1995, Cancer genetics and cytogenetics.

Identification of a haplosufficient 3.6-Mb region in human chromosome 11q14.3→q21

S. White, P. Ioannou, H. Slater, 2002, Cytogenetic and Genome Research.