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Association between the dopamine receptor D4 (DRD4) gene and obsessive-compulsive disorder
Association between the dopamine receptor D4 (DRD4) gene and obsessive-compulsive disorder
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Association between the dopamine receptor D4 (DRD4) gene and obsessive-compulsive disorder

Millet, Bruno ; Chabane, Nadia ; Delorme, Richard ; Leboyer, Marion ; Leroy, Sophie ; Poirier, Marie-France ; Bourdel, Marie-Chantal ; Mouren-Simeoni, Marie-Christine ; Rouillon, Fréderic ; Loo, Henri ; Krebs, Marie-Odile

American journal of medical genetics, 2003-01, Vol.116B (1), p.55-59 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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2
Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b
Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b
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Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b

Weese-Mayer, Debra E. ; Berry-Kravis, Elizabeth M. ; Zhou, Lili ; Maher, Brion S. ; Silvestri, Jean M. ; Curran, Mark E. ; Marazita, Mary L.

American journal of medical genetics, 2003-12, Vol.123A (3), p.267-278 [Periódico revisado por pares]

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

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3
"Everybody in the world is my friend" hypersociability in young children with Williams syndrome
"Everybody in the world is my friend" hypersociability in young children with Williams syndrome
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"Everybody in the world is my friend" hypersociability in young children with Williams syndrome

Doyle, Teresa F. ; Bellugi, Ursula ; Korenberg, Julie R. ; Graham, John

American journal of medical genetics. Part A, 2004-01, Vol.124A (3), p.263-273 [Periódico revisado por pares]

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

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4
Malignancy of recurrent, early-onset major depression: A family study
Malignancy of recurrent, early-onset major depression: A family study
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Malignancy of recurrent, early-onset major depression: A family study

Zubenko, George S. ; Zubenko, Wendy N. ; Spiker, Duane G. ; Giles, Donna E. ; Kaplan, Barry B.

American journal of medical genetics, 2001-12, Vol.105 (8), p.690-699 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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5
Prevalence of congenital cardiovascular malformations among relatives of infants with hypoplastic left heart, coarctation of the aorta, and d-transposition of the great arteries
Prevalence of congenital cardiovascular malformations among relatives of infants with hypoplastic left heart, coarctation of the aorta, and d-transposition of the great arteries
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Prevalence of congenital cardiovascular malformations among relatives of infants with hypoplastic left heart, coarctation of the aorta, and d-transposition of the great arteries

Loffredo, Christopher A. ; Chokkalingam, Anand ; Sill, Anne M. ; Boughman, Joann A. ; Clark, Edward B. ; Scheel, Janet ; Brenner, Joel I.

American journal of medical genetics. Part A, 2004-01, Vol.124A (3), p.225-230 [Periódico revisado por pares]

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

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6
Further evidence for the association between attention-deficit/hyperactivity disorder and the dopamine-β-hydroxylase gene
Further evidence for the association between attention-deficit/hyperactivity disorder and the dopamine-β-hydroxylase gene
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Further evidence for the association between attention-deficit/hyperactivity disorder and the dopamine-β-hydroxylase gene

Roman, Tatiana ; Schmitz, Marcelo ; Polanczyk, Guilherme V. ; Eizirik, Mariana ; Rohde, Luis A. ; Hutz, Mara H.

American journal of medical genetics, 2002-03, Vol.114 (2), p.154-158 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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7
Environmental, medical, and family history risk factors for Parkinson's disease: A New England-based case control study
Environmental, medical, and family history risk factors for Parkinson's disease: A New England-based case control study
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Environmental, medical, and family history risk factors for Parkinson's disease: A New England-based case control study

Taylor, C.A. ; Saint-Hilaire, M.H. ; Cupples, L.A. ; Thomas, C.A. ; Burchard, A.E. ; Feldman, R.G. ; Myers, R.H.

American journal of medical genetics, 1999-12, Vol.88 (6), p.742-749 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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8
Genome-wide linkage analysis of families with obsessive-compulsive disorder ascertained through pediatric probands
Genome-wide linkage analysis of families with obsessive-compulsive disorder ascertained through pediatric probands
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Genome-wide linkage analysis of families with obsessive-compulsive disorder ascertained through pediatric probands

Hanna, Gregory L. ; Veenstra-VanderWeele, Jeremy ; Cox, Nancy J. ; Boehnke, Michael ; Himle, Joseph A. ; Curtis, George C. ; Leventhal, Bennett L. ; Cook Jr, Edwin H.

American journal of medical genetics, 2002-07, Vol.114 (5), p.541-552 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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9
Ocular phenotypes of three genetic variants of Bardet-Biedl syndrome
Ocular phenotypes of three genetic variants of Bardet-Biedl syndrome
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Ocular phenotypes of three genetic variants of Bardet-Biedl syndrome

Héon, Elise ; Westall, Carol ; Carmi, Rivka ; Elbedour, Khalil ; Panton, Carole ; MacKeen, Leslie ; Stone, Edwin M. ; Sheffield, Val C.

American journal of medical genetics, 2005-01, Vol.132A (3), p.283-287 [Periódico revisado por pares]

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

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10
Different familial transmission patterns in bipolar I disorder with onset before and after age 25
Different familial transmission patterns in bipolar I disorder with onset before and after age 25
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Different familial transmission patterns in bipolar I disorder with onset before and after age 25

Grigoroiu-Serbanescu, Maria ; Martinez, Maria ; Nöthen, Markus M. ; Grinberg, Mihaela ; Sima, Dorina ; Propping, Peter ; Marinescu, Elvira ; Hrestic, Mihaela

American journal of medical genetics, 2001-12, Vol.105 (8), p.765-773 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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