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Refined by: collection: SciTech Premium Collection remove creation date: 1991 To 2005 remove collection: ProQuest Hospital Collection remove author/creator: Burn, J remove
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DiGeorge syndrome: Part of CATCH 22.

Wilson, DI ; Burn, J ; Scambler, P ; Goodship, J Wilson, DI (correspondence author)

Journal of Medical Genetics, 1993, Vol.30(10), pp.852-856 [Peer Reviewed Journal]

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Brief report: Autosomal dominant familial hypoparathyroidism, sensorineural deafness, and renal dysplasia.

Bilous, R ; Murty, G ; Parkinson, D ; Thakker, R ; Coulthard, M ; Burn, J ; Mathias, D ; Kendall-Taylor, P Bilous, R (correspondence author)

New England Journal of Medicine, 1992, Vol.327(15), pp.1069-1074 [Peer Reviewed Journal]

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3
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Transmission of Proteus syndrome from father to son?.

Goodship, J ; Redfearn, A ; Milligan, D ; Gardner-Medwin, D ; Burn, J Goodship, J (correspondence author)

Journal of Medical Genetics, 1991, Vol.28(11), pp.781-785 [Peer Reviewed Journal]

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Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.

Burn, J ; Takao, A ; Wilson, D ; Cross, I ; Momma, K ; Wadey, R ; Scambler, P ; Goodship, J Burn, J (correspondence author)

Journal of Medical Genetics, 1993, Vol.30(10), pp.822-824 [Peer Reviewed Journal]

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5
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A male with type I orofaciodigital syndrome.

Goodship, J ; Platt, J ; Smith, R ; Burn, J Goodship, J (correspondence author)

Journal of Medical Genetics, 1991, Vol.28(10), pp.691-694 [Peer Reviewed Journal]

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A de novo translocation t(3; 17)(q26.3; q23.1) in a child with Cornelia de Lange syndrome.

Ireland, M ; English, C ; Cross, I ; Houlsby, W ; Burn, J Ireland, M (correspondence author)

Journal of Medical Genetics, 1991, Vol.28(9), pp.639-640 [Peer Reviewed Journal]

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