Additional EFNB1 mutations in craniofrontonasal syndrome

Deeann Wallis; Felicitas Lacbawan; Mahim Jain; Vazken M. Der Kaloustian; Carlos E. Steiner; John B. Moeschler; H. Wolfgang Losken; Ilkka I. Kaitila; Stephen Cantrell; Virginia K. Proud; John C. Carey; Donald W. Day; Dorit Lev; Ahmad S. Teebi; Luther K. Robinson; H. Eugene Hoyme; Nadia Al-Torki; Jacqueline Siegel-Bartelt; John B. Mulliken; Nathaniel H. Robin; Dolores Saavedra; Elaine H. Zackai; Maximilian Muenke

doi:10.1002/ajmg.a.32388

Additional EFNB1 mutations in craniofrontonasal syndrome

Deeann Wallis
, Felicitas Lacbawan
, Mahim Jain
, Vazken M. Der Kaloustian
, Carlos E. Steiner
, John B. Moeschler
, H. Wolfgang Losken
, Ilkka I. Kaitila
, Stephen Cantrell
, Virginia K. Proud
, John C. Carey
, Donald W. Day
, Dorit Lev
, Ahmad S. Teebi
, Luther K. Robinson
, H. Eugene Hoyme
, Nadia Al-Torki
, Jacqueline Siegel-Bartelt
, John B. Mulliken
, Nathaniel H. Robin

Dolores Saavedra, Elaine H. Zackai, Maximilian Muenke

Pediatrics

University at Buffalo

Research output: Contribution to journal › Letter › peer-review

30 Scopus citations

Original language	English
Pages (from-to)	2008-2012
Number of pages	5
Journal	American Journal of Medical Genetics, Part A
Volume	146
Issue number	15
DOIs	https://doi.org/10.1002/ajmg.a.32388
State	Published - Aug 1 2008

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Wallis, D., Lacbawan, F., Jain, M., Der Kaloustian, V. M., Steiner, C. E., Moeschler, J. B., Losken, H. W., Kaitila, I. I., Cantrell, S., Proud, V. K., Carey, J. C., Day, D. W., Lev, D., Teebi, A. S., Robinson, L. K., Hoyme, H. E., Al-Torki, N., Siegel-Bartelt, J., Mulliken, J. B., ... Muenke, M. (2008). Additional EFNB1 mutations in craniofrontonasal syndrome. American Journal of Medical Genetics, Part A, 146(15), 2008-2012. https://doi.org/10.1002/ajmg.a.32388

@article{0396f09f33fb4df184c50d9fff40b599,

title = "Additional EFNB1 mutations in craniofrontonasal syndrome",

author = "Deeann Wallis and Felicitas Lacbawan and Mahim Jain and \{Der Kaloustian\}, \{Vazken M.\} and Steiner, \{Carlos E.\} and Moeschler, \{John B.\} and Losken, \{H. Wolfgang\} and Kaitila, \{Ilkka I.\} and Stephen Cantrell and Proud, \{Virginia K.\} and Carey, \{John C.\} and Day, \{Donald W.\} and Dorit Lev and Teebi, \{Ahmad S.\} and Robinson, \{Luther K.\} and Hoyme, \{H. Eugene\} and Nadia Al-Torki and Jacqueline Siegel-Bartelt and Mulliken, \{John B.\} and Robin, \{Nathaniel H.\} and Dolores Saavedra and Zackai, \{Elaine H.\} and Maximilian Muenke",

year = "2008",

month = aug,

day = "1",

doi = "10.1002/ajmg.a.32388",

language = "English",

volume = "146",

pages = "2008--2012",

journal = "American Journal of Medical Genetics, Part A",

issn = "1552-4825",

publisher = "John Wiley and Sons Inc.",

number = "15",

}

Wallis, D, Lacbawan, F, Jain, M, Der Kaloustian, VM, Steiner, CE, Moeschler, JB, Losken, HW, Kaitila, II, Cantrell, S, Proud, VK, Carey, JC, Day, DW, Lev, D, Teebi, AS, Robinson, LK, Hoyme, HE, Al-Torki, N, Siegel-Bartelt, J, Mulliken, JB, Robin, NH, Saavedra, D, Zackai, EH & Muenke, M 2008, 'Additional EFNB1 mutations in craniofrontonasal syndrome', American Journal of Medical Genetics, Part A, vol. 146, no. 15, pp. 2008-2012. https://doi.org/10.1002/ajmg.a.32388

TY - JOUR

T1 - Additional EFNB1 mutations in craniofrontonasal syndrome

AU - Wallis, Deeann

AU - Lacbawan, Felicitas

AU - Jain, Mahim

AU - Der Kaloustian, Vazken M.

AU - Steiner, Carlos E.

AU - Moeschler, John B.

AU - Losken, H. Wolfgang

AU - Kaitila, Ilkka I.

AU - Cantrell, Stephen

AU - Proud, Virginia K.

AU - Carey, John C.

AU - Day, Donald W.

AU - Lev, Dorit

AU - Teebi, Ahmad S.

AU - Robinson, Luther K.

AU - Hoyme, H. Eugene

AU - Al-Torki, Nadia

AU - Siegel-Bartelt, Jacqueline

AU - Mulliken, John B.

AU - Robin, Nathaniel H.

AU - Saavedra, Dolores

AU - Zackai, Elaine H.

AU - Muenke, Maximilian

PY - 2008/8/1

Y1 - 2008/8/1

UR - https://www.scopus.com/pages/publications/49649121280

U2 - 10.1002/ajmg.a.32388

DO - 10.1002/ajmg.a.32388

M3 - Letter

C2 - 18627045

SN - 1552-4825

VL - 146

SP - 2008

EP - 2012

JO - American Journal of Medical Genetics, Part A

JF - American Journal of Medical Genetics, Part A

IS - 15

ER -

Additional EFNB1 mutations in craniofrontonasal syndrome

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