P. Mowrey

发表

Clinical and molecular analyses of deletion 3p25-pter syndrome.

M. Lerman, B. Zbar, P. Rogan, 1993, American journal of medical genetics.

Should the 3C (craniocerebellocardiac) syndrome be included in the spectrum of velocardiofacial syndrome and DiGeorge sequence?

M. Butler, P. Mowrey, 1996, Journal of medical genetics.

A rare finding of deletion 5q in a child with juvenile myelomonocytic leukemia.

R. Neuberg, A. Meloni-Ehrig, J. Meck, 2009, Cancer genetics and cytogenetics.

46,XX, inv(6)(p21.1p23) in a pedigree with hereditary haemochromatosis.

C. Venditti, J. Knoll, G. Gerhard, 1997, Journal of medical genetics.

Dicentric (17;20)(p11.2;q11.2): an uncommon cytogenetic abnormality in myeloid malignancies.

J. Butera, L. Glasser, A. Spira, 2006, Cancer Genetics and Cytogenetics.

Insertion (12;9)(p13;q34q34): a cryptic rearrangement involving ABL1/ETV6 fusion in a patient with Philadelphia-negative chronic myeloid leukemia.

A. Meloni-Ehrig, N. C. Christacos, A. Hostetter, 2009, Cancer genetics and cytogenetics.

Translocation (2;8)(q35;q13): a recurrent abnormality in congenital embryonal rhabdomyosarcoma.

A. Meloni-Ehrig, Jay Greenberg, P. Mowrey, 2009, Cancer genetics and cytogenetics.

Cryptic ins(4;11)(q21;q23q23) detected by fluorescence in situ hybridization: a variant of t(4;11)(q21;q23) in an infant with a precursor B-cell acute lymphoblastic leukemia report of a second case.

J. Greenberg, A. Meloni-Ehrig, C. Tirado, 2007, Cancer genetics and cytogenetics.

Isolated del(14)(q21) in a case of precursor B-cell acute lymphoblastic leukemia.

N. Seibel, A. Meloni-Ehrig, H. Meany, 2005, Cancer genetics and cytogenetics.

Variant acute promyelocytic leukemia translocation (15;17) originating from two subsequent balanced translocations involving the same chromosomes 15 and 17 while preserving the PML/RARA fusion.

A. Meloni-Ehrig, C. Tirado, P. Mowrey, 2005, Cancer genetics and cytogenetics.

Five children with del (2)(q31q33) and one individual with dup (2)(q31q33) from a single family: review of brain, cardiac, and limb malformations.

J. Towfighi, R. Ladda, J. Ramer, 1990, American journal of medical genetics.

Unexpected retention and concomitant loss of subtelomeric regions in balanced chromosome anomalies by FISH.

P. N. Rao, M. Pettenati, K. May, 2002, American journal of medical genetics.

Rapid interphase analysis for prenatal diagnosis of translocation carriers using subtelomeric probes

S. Schwartz, P. Nagesh Rao, M. Pettenati, 2002, Prenatal diagnosis.

Neurologic manifestations in 18q- syndrome.

K. Hopper, R. Ladda, G. Miller, 1990, American journal of medical genetics.

Deletions of the PRKAR1A locus at 17q24.2-q24.3 in Carney complex: genotype-phenotype correlations and implications for genetic testing.

F. Faucz, C. Stratakis, I. Holm, 2014, The Journal of clinical endocrinology and metabolism.

A case of lipoblastoma with seven copies of chromosome 8.

A. Meloni-Ehrig, N. C. Christacos, P. Mowrey, 2009, Cancer genetics and cytogenetics.

Increased frequency of lymphocytic mitotic non-disjunction in recurrent spontaneous aborters.

R. C. Juberg, J. Knops, P. Mowrey, 1985, Journal of medical genetics.

Dissociation of a t(12;21) resulting in a normal cell line in two trisomic 21 sons of a nonmosaic t(12;21) father?

R. Stallard, R. C. Juberg, P. Mowrey, 2004, Human Genetics.

Interstitial del(13q) associated with blindness and mental retardation.

J. Opitz, R. C. Juberg, P. Mowrey, 1984, American journal of medical genetics.

Malformations in a child with dup (7 pter‐p15.1) and del (7 q36‐qter) as a result of familial pericentric inversion

R. Ladda, J. Ramer, P. Mowrey, 1991, Clinical genetics.

Molecularly defined interstitial tandem duplication 6p case with mild manifestations.

G. Mirza, J. Ragoussis, C. Turner, 2001, American journal of medical genetics.

Origin of nondisjunction in trisomy 21 syndrome: all studies compiled, parental age analysis, and international comparisons.

R. C. Juberg, P. Mowrey, 1983, American journal of medical genetics.

Long-term persistence of nonpathogenic clonal chromosome abnormalities in donor hematopoietic cells after allogeneic stem cell transplantation.

R. Srinivasan, R. Childs, A. Meloni-Ehrig, 2009, Cancer genetics and cytogenetics.

Short communication Long-term persistence of nonpathogenic clonal chromosome abnormalities in donor hematopoietic cells after allogeneic stem cell transplantation

R. Srinivasan, R. Childs, A. Meloni-Ehrig, 2009 .

Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study

S. Schwartz, U. Surti, L. Christ, 2006, Journal of Medical Genetics.

Incidence and patterns of ALK FISH abnormalities seen in a large unselected series of lung carcinomas

M. Slovak, Z. Dai, Q. Pan, 2012, Molecular Cytogenetics.

Short communication Insertion (12;9)(p13;q34q34): a cryptic rearrangement involving ABL1/ETV6 fusion in a patient with Philadelphia-negative chronic myeloid leukemia

A. Meloni-Ehrig, N. C. Christacos, A. Hostetter, 2009 .

Short communication Isolated del(14)(q21) in a case of precursor B-cell acute lymphoblastic leukemia

N. Seibel, A. Meloni-Ehrig, H. Meany, 2005 .

Deletion 6p as the sole chromosome abnormality in a patient with therapy-related myelodysplastic syndrome: case report and review of the literature.

A. Meloni-Ehrig, J. Meck, P. Mowrey, 2010, Cancer genetics and cytogenetics.