Antenatal diagnosis of DiGeorge syndrome.

DeborahA. Driscoll , MarciaL. Budarf , BeverlyS. Emanuel
The Lancet 338 ( 8779) 1390 -1391

24
1991
The Human "Peripheral-Type" Benzodiazepine Receptor: Regional Mapping of the Gene and Characterization of the Receptor Expressed from cDNA

YUEH J. CHANG , R. TYLER McCABE , HANNA RENNERT , MARCIA L. BUDARF
DNA and Cell Biology 11 ( 6) 471 -480

30
1992
A multilevel analysis of cognitive dysfunction and psychopathology associated with chromosome 22q11.2 deletion syndrome in children.

TONY J. SIMON , JOEL P. BISH , CARRIE E. BEARDEN , LIJUN DING
Development and Psychopathology 17 ( 3) 753 -784

70
2005
Developmental presentation of 22q11.2 deletion (DiGeorge/velocardiofacial syndrome).

PAUL P. WANG , CYNTHIA SOLOT , EDWARD M. MOSS , MARSHA GERDES
Journal of Developmental and Behavioral Pediatrics 19 ( 5) 342 -345

20
1998
PCR assay for screening patients at risk for 22q11.2 deletion.

DEBORAH A. DRISCOLL , BEVERLY S. EMANUEL , LAURA E. MITCHELL , MARCIA L. BUDARF
Genetic Testing 1 ( 2) 109 -113

18
1997
The 22q11.2 deletion: screening, diagnostic workup, and outcome of results; report on 181 patients.

DONNA M. McDONALD-McGINN , DON LaROSSA , ELIZABETH GOLDMUNTZ , KATHLEEN SULLIVAN
Genetic Testing 1 ( 2) 99 -108

138
1997
Integration of physical, breakpoint and genetic maps of chromosome 22. Localization of 587 yeast artificial chromosomes with 238 mapped markers

C. J.Bell , M. L.Budarf , B. W.Nieuwenhuijsen , B. L.Barnoski
Human Molecular Genetics 4 ( 1) 59 -69

26
1995
Nucleolar organizing regions within interphase nuclei

JE Sylvester , F KAPLAN , J MURRAY , B EMANUEL
AMERICAN JOURNAL OF HUMAN GENETICS 49 ( 4) 308 -308

1
1991
PHYSICAL MAPPING OF THE NEUROFIBROMATOSIS TYPE-2 (NF-2) LOCUS ON CHROMOSOME-22

AG Menon , HL Snyder , C Murdock , JA TROFATTER
AMERICAN JOURNAL OF HUMAN GENETICS 49 ( 4) 384 -384

2
1991
RISK-FACTORS FOR RETINOBLASTOMA-RESULTS OF A CASE-CONTROL STUDY

G BUNIN , A MEADOWS , B EMANUEL , W WOODS
PROCEEDINGS OF THE AMERICAN ASSOCIATION FOR CANCER RESEARCH 29 256 -256

1988
EST-DRIVEN GENE IDENTIFICATION IN GENOMIC DNA-SEQUENCE

LC BAILEY , M BUDARF , GC OVERTON , W GONG
AMERICAN JOURNAL OF HUMAN GENETICS 57 ( 4) 285 -285

1995
A GENETIC-LINKAGE MAP OF 22 LOCI ON CHROMOSOME-22

JP DUMANSKI , E CARLBOM , P COLLINS , M NORDENSKJOLD
CYTOGENETICS AND CELL GENETICS 58 ( 3-4) 2047 -2047

1991
3Q+-CHROMOSOME ABNORMALITY IN GLIOBLASTOMA

C GRIFFIN , S GROSSMAN , J HILTON , D HAUQUITZ
PROCEEDINGS OF THE AMERICAN ASSOCIATION FOR CANCER RESEARCH 27 36 -36

1986
CHROMOSOMAL DISTRIBUTION OF RIBOSOMAL DNA-SEQUENCES

AI GROSSMAN , RD SCHMICKEL , B EMANUEL
AMERICAN JOURNAL OF HUMAN GENETICS 35 ( 6) A173 -A173

1983
MOLECULAR GENETIC-STUDIES OF THE 9-22 TRANSLOCATION OF ACUTE LYMPHOCYTIC-LEUKEMIA

CA GRIFFIN , J ERIKSON , PC NOWELL , M VALTIERI
JOURNAL OF CELLULAR BIOCHEMISTRY 34 -34

1986
PRENATAL-DIAGNOSIS OF CAT EYE SYNDROME BY FLUORESCENCE IN-SITU HYBRIDIZATION (FISH)

DA DRISCOLL , B SELLINGER , ML BUDARF , BS EMANUEL
AMERICAN JOURNAL OF HUMAN GENETICS 53 ( 3) 1401 -1401

1993
DNA-REPLICATION PATTERNS IN X AND Y-CHROMOSOME ABNORMALITIES BY A BUDR-DYE TECHNIQUE

BS EMANUEL , EH ZACKAI , WJ MELLMAN
AMERICAN JOURNAL OF HUMAN GENETICS 29 ( 6) A39 -A39

1
1977
1995
CAT EYE SYNDROME PATIENT WITH INTERSTITIAL DUPLICATION OF CHROMOSOME 22Q11. 2

BT SELLINGER , YO TATSUMURA , AJ MEARS , HE MCDERMID
CYTOGENETICS AND CELL GENETICS 71 ( 4) 394 -394

1995