Shprintzen-Goldberg syndrome results from mutations in fibrillin-1, not monosomy 22q11 [3] (multiple letters)

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@article{a8015b1bb7c34db283beab91466cb221,

title = "Shprintzen-Goldberg syndrome results from mutations in fibrillin-1, not monosomy 22q11 [3] (multiple letters)",

author = "E. Hatchwell and Johnson, \{M. C.\} and Watson, \{M. S.\} and Dowton, \{S. B.\} and Strauss, \{A. W.\}",

year = "1997",

doi = "10.1016/S0022-3476(97)70144-6",

language = "English",

volume = "131",

pages = "164--165",

journal = "Journal of Pediatrics",

issn = "0022-3476",

number = "1 I",

}

TY - JOUR

T1 - Shprintzen-Goldberg syndrome results from mutations in fibrillin-1, not monosomy 22q11 [3] (multiple letters)

AU - Hatchwell, E.

AU - Johnson, M. C.

AU - Watson, M. S.

AU - Dowton, S. B.

AU - Strauss, A. W.

PY - 1997

Y1 - 1997

UR - https://www.scopus.com/pages/publications/0030722119

U2 - 10.1016/S0022-3476(97)70144-6

DO - 10.1016/S0022-3476(97)70144-6

M3 - Letter

C2 - 9255212

AN - SCOPUS:0030722119

SN - 0022-3476

VL - 131

SP - 164

EP - 165

JO - Journal of Pediatrics

JF - Journal of Pediatrics

IS - 1 I

ER -