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1
Resolution of coronary arteritis following tuberculosis treatment
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Resolution of coronary arteritis following tuberculosis treatment

Barreto-Neto, Nestor ; Segre, Alexandre W ; Guedes, Lissiane K N ; Seguro, Luciana P C ; Pereira, Rosa M R

Journal of clinical tuberculosis and other mycobacterial diseases, 2022, Vol.26, p.100295-100295

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2
Compensatory education for cultural deprivation, B. S. Bloom, A. Davis, R. Hess. 1965
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Compensatory education for cultural deprivation, B. S. Bloom, A. Davis, R. Hess. 1965

Segré, Monique

Revue française de pédagogie, 1967, Vol.1 (1), p.39-40

PERSÉE : Université de Lyon, CNRS & ENS de Lyon

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3
High Energy Alpha Particles Associated with Fission
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High Energy Alpha Particles Associated with Fission

Wollan, E. O ; Moak, Charles D ; Sawyer, R. B

1947

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4
Deep pyoderma caused by Burkholderia cepacia complex associated with ciclosporin administration in dogs: a case series
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Deep pyoderma caused by Burkholderia cepacia complex associated with ciclosporin administration in dogs: a case series

Banovic, Frane ; Koch, Sandra ; Robson, David ; Jacob, Megan ; Olivry, Thierry

Veterinary Dermatology, 2015, Vol.26 (4), p.287-e64

Blackwell Publishing Ltd

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5
Cervical tumoral calcinosis with secondary hyperparathyroidism in a chronic hemodialysis patient
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Cervical tumoral calcinosis with secondary hyperparathyroidism in a chronic hemodialysis patient

Sunder, Sham ; Verma, Himanshu ; Venkataramanan, Krishnamoorthy

Hemodialysis International, 2013, Vol.17 (3), p.458-462

Blackwell Publishing Ltd

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6
Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters
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Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters

Harrison, Victoria ; Connell, Lyndsey ; Hayesmoore, Jesse ; McParland, Joanna ; Pike, Michael G. ; Blair, Edward

American Journal of Medical Genetics Part A, 2011, Vol.155A (11), p.2826-2831

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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7
A 10.46 Mb 12p11.1-12.1 interstitial deletion coincident with a 0.19 Mb NRXN1 deletion detected by array CGH in a girl with scoliosis and autism
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A 10.46 Mb 12p11.1-12.1 interstitial deletion coincident with a 0.19 Mb NRXN1 deletion detected by array CGH in a girl with scoliosis and autism

Soysal, Yasemin ; Vermeesch, Joris ; Davani, Nooshin Ardeshir ; Hekimler, Kuyaş ; İmirzalıoğlu, Necat

American Journal of Medical Genetics Part A, 2011, Vol.155A (7), p.1745-1752

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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8
Mosaic partial trisomy 19p12-q13.11 due to a small supernumerary marker chromosome: A locus associated with Asperger syndrome?
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Mosaic partial trisomy 19p12-q13.11 due to a small supernumerary marker chromosome: A locus associated with Asperger syndrome?

Faucz, Fabio Rueda ; Souza, Josiane ; Filho, Aguinaldo Bonalumi ; Sotomaior, Vanessa Santos ; Frantz, Egon ; Antoniuk, Sergio ; Rosenfeld, Jill A. ; Raskin, Salmo

American Journal of Medical Genetics Part A, 2011, Vol.155A (9), p.2308-2310

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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9
A case of autism with an interstitial 1q deletion (1q23.3-24.2) and a de novo translocation of chromosomes 1q and 5q
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A case of autism with an interstitial 1q deletion (1q23.3-24.2) and a de novo translocation of chromosomes 1q and 5q

Della Monica, Matteo ; Lonardo, Fortunato ; Faravelli, Francesca ; Pierluigi, Mauro ; Luquetti, Daniela Varela ; De Gregori, Manuela ; Zuffardi, Orsetta ; Scarano, Gioacchino

American Journal of Medical Genetics Part A, 2007, Vol.143A (22), p.2733-2737

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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10
Fanconi's Syndrome in a Dog With Primary Hypoparathyroidism
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Fanconi's Syndrome in a Dog With Primary Hypoparathyroidism

Freeman, Lisa M. ; Breitschwerdt, Edward B. ; Keene, Bruce W. ; Hansen, Bernie

Journal of Veterinary Internal Medicine, 1994, Vol.8 (5), p.349-354

Oxford, UK: Blackwell Publishing Ltd

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