Concepedia

Author

Philip N. Mowrey

Quest Diagnostics (United States)

Also Known As

C Croft, P Mowrey, P N Mowrey, P. Mowrey, P.N. Mowrey, Philip Mowrey, Philip N Mowrey, Philip N. Mowrey

34

Publications

627

Citations

12

H-Index

42

Concepts

All Affiliations

Quest Diagnostics (United States)Penn State Milton S. Hershey Medical CenterChildren's Medical CenterEunice Kennedy Shriver National Institute of Child Health and Human DevelopmentNational Institutes of Health
PN

About

Philip N. Mowrey is an author at Quest Diagnostics (United States) specializing in medicine, pathology, and genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

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2

Public Health

2

2

102

3

Cell Biology

2

2

48

4

Health Sciences

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1

30

5

Biology

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84

Philip N. Mowrey

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11

Publications

493

Citations

10

H-Index

YearCitations

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

Richard C. Juberg, Philip N. Mowrey

American Journal of Medical Genetics

1983

91

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

Mark J. Pettenati, C. Von Kap-Herr, Bethy Jackle,

Prenatal Diagnosis

2002

84

Neurologic manifestations in 18q– syndrome

Geoffrey Miller, Philip N. Mowrey, Kenneth D. Hopper,

American Journal of Medical Genetics

1990

83

Deletions of the PRKAR1A Locus at 17q24.2-q24.3 in Carney Complex: Genotype-Phenotype Correlations and Implications for Genetic Testing

Anélia Horvath, Edra London, Fábio R. Faucz,

The Journal of Clinical Endocrinology & Metabolism

2013

67

Clinical and molecular analyses of deletion 3p25‐pter syndrome

Philip N. Mowrey, Michael J. Chorney, Charles P. Venditti,

American Journal of Medical Genetics

1993

44

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

Zunyan Dai, JoAnn C. Kelly, Aurelia Meloni‐Ehrig,

Molecular Cytogenetics

2012

31

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

JoAnn C. Kelly, Nasrin Shahbazi, Jay Scheerle,

Cancer Genetics and Cytogenetics

2009

30

Molecularly defined interstitial tandem duplication 6p case with mild manifestations

David Ng, Philip N. Mowrey, Jiannis Ragoussis,

American Journal of Medical Genetics

2001

20

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

Richard C. Juberg, Judy Knops, Philip N. Mowrey

Journal of Medical Genetics

1985

18

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

Aurelia Meloni‐Ehrig, Bridget Smith, JoAnna Zgoda,

Cancer Genetics and Cytogenetics

2009

15

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