[FAMILIAL MALFORMATION COMPLEX WITH UMBILICAL HE... [J Genet Hum. 1964] - PubMed

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A FAMILIAL SYNDROME OF MULTIPLE CONGENITAL DEFECTS. [Bull Johns Hopkins Hosp. 1964]
A FAMILIAL SYNDROME OF MULTIPLE CONGENITAL DEFECTS.
BOWEN P, LEE CS, ZELLWEGER H, LINDENBERG R. Bull Johns Hopkins Hosp. 1964 Jun; 114:402-14.
[The EMG-syndrome: exomphalos, macroglossia, gigantism and disturbed carbohydrate metabolism]. [Z Kinderheilkd. 1969]
[The EMG-syndrome: exomphalos, macroglossia, gigantism and disturbed carbohydrate metabolism].
Wiedemann HR. Z Kinderheilkd. 1969; 106(3):171-85.
[The exomphalos-macroglossia-gigantism syndrome]. [Zentralbl Gynakol. 1973]
[The exomphalos-macroglossia-gigantism syndrome].
Heissmeyer U. Zentralbl Gynakol. 1973 Feb 2; 95(5):158-66.
Review Macroglossia, omphalocele, visceromegaly, cytomegaly of the adrenal cortex and neonatal hypoglycemia. [Birth Defects Orig Artic Ser. ...]
Review Macroglossia, omphalocele, visceromegaly, cytomegaly of the adrenal cortex and neonatal hypoglycemia.
Cohen MM Jr. Birth Defects Orig Artic Ser. 1971 Jun; 7(7):226-32.
Review The "E.M.G." syndrome (Exomphalos, Macroglossia, Gigantism). [Prog Pediatr Surg. 1970]
Review The "E.M.G." syndrome (Exomphalos, Macroglossia, Gigantism).
Irving IM. Prog Pediatr Surg. 1970; 1:1-61.

Analysis of wilms tumors using SNP mapping array-based comparative genomic hybridization. [PLoS One. 2011]
Analysis of wilms tumors using SNP mapping array-based comparative genomic hybridization.
Hawthorn L, Cowell JK. PLoS One. 2011 Apr 22; 6(4):e18941. Epub 2011 Apr 22.
Beckwith-Wiedemann syndrome and uniparental disomy 11p: fine mapping of the recombination breakpoints and evaluation of several techniques. [Eur J Hum Genet. 2011]
Beckwith-Wiedemann syndrome and uniparental disomy 11p: fine mapping of the recombination breakpoints and evaluation of several techniques.
Romanelli V, Meneses HN, Fernández L, Martínez-Glez V, Gracia-Bouthelier R, F Fraga M, Guillén E, Nevado J, Gean E, Martorell L, et al. Eur J Hum Genet. 2011 Apr; 19(4):416-21. Epub 2011 Jan 19.
Epigenetic silencing of beta-spectrin, a TGF-beta signaling/scaffolding protein in a human cancer stem cell disorder: Beckwith-Wiedemann syndrome. [J Biol Chem. 2010]
Epigenetic silencing of beta-spectrin, a TGF-beta signaling/scaffolding protein in a human cancer stem cell disorder: Beckwith-Wiedemann syndrome.
Yao ZX, Jogunoori W, Choufani S, Rashid A, Blake T, Yao W, Kreishman P, Amin R, Sidawy AA, Evans SR, et al. J Biol Chem. 2010 Nov 12; 285(46):36112-20. Epub 2010 Aug 25.

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[FAMILIAL MALFORMATION COMPLEX WITH UMBILICAL HERNIA AND MACROGLOSSIA--A "NEW SY...
[FAMILIAL MALFORMATION COMPLEX WITH UMBILICAL HERNIA AND MACROGLOSSIA--A "NEW SYNDROME"?].
J Genet Hum. 1964 Sep ;13:223-32.

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Bone infarct-associated osteosarcoma.
Bone infarct-associated osteosarcoma.
Cancer. 1992 Nov 15 ;70(10):2418-30.

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Canadian National Breast Screening Study: 1. Breast cancer detection and death r...
Canadian National Breast Screening Study: 1. Breast cancer detection and death rates among women aged 40 to 49 years.
CMAJ. 1992 Nov 15 ;147(10):1459-76.

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Homeopathy treats people, not the soles of their feet.
Homeopathy treats people, not the soles of their feet.
CMAJ. 1992 Nov 15 ;147(10):1407; author reply 1408-9.

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[A CASE OF FAMILIAL ALPHA-1-ANTITRYPSIN DEFICIENCY].
[A CASE OF FAMILIAL ALPHA-1-ANTITRYPSIN DEFICIENCY].
Helv Paediatr Acta. 1964 Oct ;19:296-303.

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