Additional EFNB1 mutations in craniofrontonasal syndrome

American Journal of Medical Genetics, Part A

Volumn 146, Issue 15, 2008, Pages 2008-2012

  Wallis, Deeann ^a,u   Lacbawan, Felicitas ^a   Jain, Mahim ^a   Der Kaloustian, Vazken M ^b   Steiner, Carlos E ^c   Moeschler, John B ^d   Losken, H Wolfgang ^e   Kaitila, Ilkka I ^f   Cantrell, Stephen ^g   Proud, Virginia K ^h   Carey, John C ⁱ   Day, Donald W ^j   Lev, Dorit ^k   Teebi, Ahmad S ^l   Robinson, Luther K ^m   Hoyme, H Eugene ⁿ   Al Torki, Nadia ^o   Siegel Bartelt, Jacqueline ^p   Mulliken, John B ^q   Robin, Nathaniel H ^r   Saavedra, Dolores ^s   Zackai, Elaine H ^t   Muenke, Maximilian ^a   more..

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b MCGILL UNIVERSITY HEALTH CENTRE   (Canada)

^c UNIVERSITY OF CAMPINAS   (Brazil)

^d DARTMOUTH HITCHCOCK MEDICAL CENTER   (United States)

^e UNIVERSITY OF PITTSBURGH   (United States)

^f UNIVERSITY OF HELSINKI   (Finland)

^g RUTGERS SCHOOL OF DENTAL MEDICINE   (United States)

^h CHILDREN S HOSPITAL OF THE KING S DAUGHTERS   (United States)

ⁱ UNIVERSITY OF UTAH HEALTH SCIENCES CENTER   (United States)

^j Private Practice   (United States)

^k Wolfson Medical Center   (Israel)

^l WEILL CORNELL MEDICAL COLLEGE   (United States)

^m UNIVERSITY AT BUFFALO   (United States)

ⁿ STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^o Kuwait Medical Genetics Centre   (Kuwait)

^p Genetics Institute   (United States)

^q BOSTON CHILDREN S HOSPITAL   (United States)

^r UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

^s HOSPITAL GENERAL DR MANUEL GEA GONZÁLEZ   (Mexico)

^t CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^u Texas Institute for Genomic Medicine   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME DELETION; CLEFT LIP NOSE; CRANIOFACIAL SYNOSTOSIS; CRANIOFRONTONASAL SYNDROME; EMBRYO DEVELOPMENT; FEMALE; GENE EXPRESSION; GENE MAPPING; GENE MUTATION; GENETIC ANALYSIS; GENETIC DISORDER; HUMAN; HYPERTELORISM; LETTER; LINKAGE ANALYSIS; MALE; MICROSATELLITE MARKER; PHENOTYPE; PRIORITY JOURNAL; SKELETON MALFORMATION; X CHROMOSOME LINKED DISORDER; ARTICLE; DNA SEQUENCE; GENETICS; MUTATION; POLYMERASE CHAIN REACTION; SYNDROME; X CHROMOSOME;

DNA; EFNB1 PROTEIN, HUMAN; EPHRIN B1;

CHROMOSOMES, HUMAN, X; CRANIOSYNOSTOSES; DNA; EPHRIN-B1; FEMALE; HUMANS; MALE; MUTATION; POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS, DNA; SYNDROME;

EID: 49649121280     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32388     Document Type: Letter

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