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1
Consanguinity and congenital heart disease in Saudi Arabia
Consanguinity and congenital heart disease in Saudi Arabia
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Consanguinity and congenital heart disease in Saudi Arabia

Becker, Susan M. ; Al Halees, Zohair ; Molina, Corazon ; Paterson, Richard M.

American journal of medical genetics, 2001-02, Vol.99 (1), p.8-13

New York: John Wiley & Sons, Inc

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2
Absence of correlation between utrophin localization and quantity and the clinical severity in duchenne / becker dystrophies
Absence of correlation between utrophin localization and quantity and the clinical severity in duchenne / becker dystrophies
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Absence of correlation between utrophin localization and quantity and the clinical severity in duchenne / becker dystrophies

M Vainzof Maria Rita Passos-Bueno; N Man; M Zatz

New York v.58, n.4 , p.305-9, 1995 American Journal of Medical Genetics

New York 1995

Item não circula. Consulte sua biblioteca.(Acessar)

3
Genetic variation of the human glycine receptor subunit genes GLRA3 and GLRB and susceptibility to idiopathic generalized epilepsies
Genetic variation of the human glycine receptor subunit genes GLRA3 and GLRB and susceptibility to idiopathic generalized epilepsies
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Genetic variation of the human glycine receptor subunit genes GLRA3 and GLRB and susceptibility to idiopathic generalized epilepsies

Sobetzko, Diana ; Sander, Thomas ; Becker, Cord-Michael

American journal of medical genetics, 2001-08, Vol.105 (6), p.534-538 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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4
Absence of correlation between utrophin localization and quantity and the clinical severity in duchenne / becker dystrophies
Absence of correlation between utrophin localization and quantity and the clinical severity in duchenne / becker dystrophies
Material Type:
Artigo 		Adicionar ao Meu Espaço

Absence of correlation between utrophin localization and quantity and the clinical severity in duchenne / becker dystrophies

Mariz Vainzof Maria Rita Passos-Bueno; N Man; Mayana Zatz

New York v.58, n.4 , p.305-9, 1995 American Journal of Medical Genetics

New York 1995

Item não circula. Consulte sua biblioteca.(Acessar)

5
Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers
Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers
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Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers

Denilce Ritsuko Sumita Mariz Vainzof; Simone Campiotto; Antonia M Cerqueira; Marta Canovas; Paulo A Otto; Maria Rita Passos-Bueno; Mayana Zatz

American Journal of Medical Genetics v. 80, p. 356-361, 1998

New York 1998

Item não circula. Consulte sua biblioteca.(Acessar)

6
Ocular manifestations in Proteus syndrome
Ocular manifestations in Proteus syndrome
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Ocular manifestations in Proteus syndrome

De Becker, Inge ; Gajda, David J. ; Gilbert-Barness, Enid ; Cohen Jr, M. Michael

American journal of medical genetics, 2000-06, Vol.92 (5), p.350-352

New York: John Wiley & Sons, Inc

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7
Oligohydramnios hampering prenatal diagnosis of Meckel syndrome
Oligohydramnios hampering prenatal diagnosis of Meckel syndrome
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Oligohydramnios hampering prenatal diagnosis of Meckel syndrome

Verjaal, Marianne ; Meyer, Adriaan H. ; Becker-Bloemkolk, Mies J. ; Leschot, Nico J. ; der Weduwen, Johanna J. ; Gras, Joop G. F. M.

American journal of medical genetics, 1980, Vol.7 (1), p.85-86

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

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8
Occurrence of cardiac malformations in relatives of children with transposition of the great arteries
Occurrence of cardiac malformations in relatives of children with transposition of the great arteries
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Occurrence of cardiac malformations in relatives of children with transposition of the great arteries

Becker, Troy A. ; Van Amber, Roberta ; Moller, James H. ; Pierpont, Mary Ella M.

American journal of medical genetics, 1996-12, Vol.66 (1), p.28-32

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

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9
Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paraganglioma
Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paraganglioma
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Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paraganglioma

Niemann, Stephan ; Becker-Follmann, Johannes ; Nürnberg, Gudrun ; Rüschendorf, Franz ; Sieweke, Nicole ; Hügens-Penzel, Monika ; Traupe, Horst ; Wienker, Thomas F. ; Reis, André ; Müller, Ulrich

American journal of medical genetics, 2001-01, Vol.98 (1), p.32-36

New York: John Wiley & Sons, Inc

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10
Usefulness of a CACA repeat polymorphism in genotype assignments in Duchenne/Becker muscular dystrophy
Usefulness of a CACA repeat polymorphism in genotype assignments in Duchenne/Becker muscular dystrophy
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Usefulness of a CACA repeat polymorphism in genotype assignments in Duchenne/Becker muscular dystrophy

Miller, Marvin ; Boehm, Corinne ; Cotton, Matthew ; Kazazian Jr, Haig H.

American journal of medical genetics, 1992-11, Vol.44 (4), p.473-476

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

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Deste Autor:

  1. Zatz, M
  2. Passos-Bueno, M
  3. Vainzof, M
  4. Otto, P
  5. Becker, J

Neste Assunto:

  1. Humans
  2. Genetics & Heredity
  3. Life Sciences & Biomedicine
  4. Science & Technology
  5. Biological And Medical Sciences

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