引用次数
引用: 34,180
H-指数: 97
I10-指数 : 327
出版物: 653
CYTOGENETIC ABNORMALITIES IN PEDIATRIC SOLID TUMORS
BS EMANUEL
MEDICAL AND PEDIATRIC ONCOLOGY 15 ( 6) 308 -308
1987
MOLECULAR-CYTOGENETIC STUDIES OF THE 11-22 TRANSLOCATION
BS EMANUEL , CA GRIFFIN , C MCKEON , D STEHELIN
PEDIATRIC RESEARCH 20 ( 4) A263 -A263
1986
PERICENTRIC INVERTED-X-PHENOTYPIC EFFECT ON HETEROZYGOTE AND HEMIZYGOTE
DAH WHITEMAN , EH ZACKAI , BS EMANUEL , MT MENNUTI
AMERICAN JOURNAL OF HUMAN GENETICS 35 ( 6) A160 -A160
1983
TERTIARY MONOSOMY, DER (22) T (10-22)(Q26-Q11) PAT, IN ASSOCIATION WITH DEGEORGE SYNDROME
EH ZACKAI , BS EMANUEL , RI KELLEY
AMERICAN JOURNAL OF HUMAN GENETICS 33 ( 6) A128 -A128
1981
MOLECULAR CYTOGENETICS OF HUMAN-TUMOR HSRS
BS EMANUEL , G BALABANMALENBAUM , F GILBERT
AMERICAN JOURNAL OF HUMAN GENETICS 32 ( 6) A68 -A68
1980
CAUTION IN DELINEATION AND CLINICAL APPLICATION OF NEW CHROMOSOMAL SYNDROMES
EH ZACKAI , BS EMANUEL
AMERICAN JOURNAL OF HUMAN GENETICS 30 ( 6) A100 -A100
1978
DNA-REPLICATION PATTERNS IN STRUCTURALLY ABNORMAL CHROMOSOMES
LA MOREAU , BS EMANUEL
AMERICAN JOURNAL OF HUMAN GENETICS 30 ( 6) A87 -A87
1978
Progress towards cloning the 22q11 breakpoint of the recurrent constitutional t (11-22)
BL BARNOSKI , BS EMANUEL , CJ BELL , M STRAAKA
AMERICAN JOURNAL OF HUMAN GENETICS 57 ( 4) 594 -594
1995
Optical mapping of 22q11. 2 Low Copy Repeats reveals structural interindividual hypervariability
Lisanne Vervoort , Wolfram Demaerel , Matthew Hestand , Ann Swillen
19th annual BeSHG meeting: Precision Medicine: Application of Genetics in Prevention and Treatment, Date: 2019/03/15-2019/03/15, Location: Liège, Belgium 33 -34
2019
Cytogenetic and endocrine findings in a female with 45, X, t (Y; 18)(p11; p11)
FG Cassorla , B s Emanuel , JS Parks , CH Wu
Clinical Genetics 19 ( 5) 312 -320
6
1981
Deletion of 22q11. 2
Wendy R KATES , Beverly S EMANUEL
Developmental disabilities research reviews 14 ( 1)
2008
Children's Hospital ofPhiladelphia University ofPennsylvania
BEVERLY S EMANUEL
The 22q11.2 deletion syndrome.
Sulagna C. Saitta , Donna Mcdonald-Mcginn , Beverly S. Emanuel , Elaine H. Zackai
Advances in Pediatrics 48 39 -73
104
2001
The chromosome disorders. An introduction for clinicians
Beverly S. Emanuel
American Journal of Human Genetics 29 ( 1) 114 -114
1977
Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization
David H. Ledbetter , Beverly S. Emanuel , Susan A. Ledbetter , Akira Kuwano
American Journal of Human Genetics 49 ( 4) 707 -714
149
1991
Chromosome abnormalities in pediatric brain tumors.
Beverly S. Emanuel , Lucy B. Rorke , Constance A. Griffin , Anita L. Hawkins
Cancer Research 48 ( 1) 175 -180
204
1988
Chromosome variations in human evolution.
Beverly S. Emanuel
American Journal of Human Genetics 29 ( 1) 113 -114
6
1977
Interrupção do arco aórtico tipo B em uma paciente com síndrome de olho de gato
Fernanda Teixeira da Silva Bellucco , Beverly S. Emanuel , Sintia Iole Belangero , Maria Isabel Melaragno
Arquivos Brasileiros De Cardiologia 92 ( 5)
2009
Evidence for a 17p Tumor Related Locus Distinct from p53 in Pediatric Primitive Neuroectodermal Tumors
Jaclyn A. Biegel , Beverly S. Emanuel , Carol D. Burk , Frederic G. Barr
Cancer Research 52 ( 12) 3391 -3395
128
1992
Occupations of Parents of Children with Retinoblastoma: A Report from the Children's Cancer Study Group
Beverly S. Emanuel , Greta R. Bunin , Anna T. Meadows , Jonathan D. Buckley
Cancer Research 50 ( 22) 7129 -7133
39
1990