Concepedia

Author

Beatrice Sellinger

Children's Hospital of Philadelphia

Also Known As

B Sellinger, B T Sellinger, Beatrice Sellinger, Beatrice T. Sellinger

18

Publications

1K

Citations

14

H-Index

49

Concepts

All Affiliations

Children's Hospital of PhiladelphiaUniversity of PennsylvaniaHospital of the University of Pennsylvania
BS

About

Beatrice Sellinger is an author at Children's Hospital of Philadelphia specializing in medicine, genetics, and molecular genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

7

7

643

2

Health Sciences

1

1

16

3

Natural Sciences

1

1

35

4

Public Health

1

1

488

5

Biology

1

1

35

Beatrice Sellinger

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14

Publications

953

Citations

13

H-Index

YearCitations

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.

Deborah A. Driscoll, J Salvin, Beatrice Sellinger,

Journal of Medical Genetics

1993

488

Molecular characterization of the marker chromosome associated with cat eye syndrome.

Alan J. Mears, Alessandra M.V. Duncan, Marcia L. Budarf,

PubMed

1994

94

The DiGeorge syndrome minimal critical region contains a goosecoid-like (GSCL) homeobox gene that is expressed early in human development.

S Gottlieb, Beverly S. Emanuel, Deborah A. Driscoll,

PubMed

1997

66

Comparative mapping of the constitutional and tumor-associated 11;22 translocations.

Marcia L. Budarf, Beatrice Sellinger, C.A. Griffin,

PubMed

1989

54

Localization of the Human Gene for Macrophage Migration Inhibitory Factor (MIF) to Chromosome 22q11.2

Marcia L. Budarf, Terrence P. McDonald, Beatrice Sellinger,

Genomics

1997

50

Isolation and regional localization of 35 unique anonymous DNA markers for human chromosome 22

Marcia L. Budarf, Heather E. McDermid, Beatrice Sellinger,

Genomics

1991

35

Molecular and cytogenetic analysis of chromosomal arms 2q and 13q in alveolar rhabdomyosarcoma

Frederic G. Barr, Jaclyn A. Biegel, Beatrice Sellinger,

Genes Chromosomes and Cancer

1991

35

Localization of the human procollagen alpha 1(IV) gene to chromosome 13q34 by in situ hybridization.

Beverly S. Emanuel, Beatrice Sellinger, Lorraine J. Gudas,

PubMed

1986

33

Type I Oculocutaneous Albinism Associated with a Full-Length Deletion of the Tyrosinase Gene

Rhonda E. Schnur, Beatrice Sellinger, Stuart A. Holmes,

Journal of Investigative Dermatology

1996

24

Classical Noonan syndrome is not associated with deletions of 22q11

Nathaniel H. Robin, Beatrice Sellinger, Donna M. McDonald‐McGinn,

American Journal of Medical Genetics

1995

16

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