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1
Discriminant analysis of the Ullrich-Turner syndrome neurocognitive profile
Discriminant analysis of the Ullrich-Turner syndrome neurocognitive profile
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Discriminant analysis of the Ullrich-Turner syndrome neurocognitive profile

Ross, Judith L. ; Kushner, Harvey ; Zinn, Andrew R.

American journal of medical genetics, 1997-10, Vol.72 (3), p.275-280 [Periódico revisado por pares]

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

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2
Evaluation of carrier detection rate for Duchenne and Becker muscular dystrophies using serum creatine kinase (ck) and pyruvate-kinase (pk) through discriminant analysis
Evaluation of carrier detection rate for Duchenne and Becker muscular dystrophies using serum creatine kinase (ck) and pyruvate-kinase (pk) through discriminant analysis
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Evaluation of carrier detection rate for Duchenne and Becker muscular dystrophies using serum creatine kinase (ck) and pyruvate-kinase (pk) through discriminant analysis

Mayana Zatz Paulo Alberto Otto

New York v.25, n.2 , p.219-31, 1986 American Journal of Medical Genetics

New York 1986

Item não circula. Consulte sua biblioteca.(Acessar)

3
Evaluation of carrier detection rate for Duchenne and Becker muscular dystrophies using serum creatine kinase (ck) and pyruvate-kinase (pk) through discriminant analysis
Evaluation of carrier detection rate for Duchenne and Becker muscular dystrophies using serum creatine kinase (ck) and pyruvate-kinase (pk) through discriminant analysis
Material Type:
Artigo 		Adicionar ao Meu Espaço

Evaluation of carrier detection rate for Duchenne and Becker muscular dystrophies using serum creatine kinase (ck) and pyruvate-kinase (pk) through discriminant analysis

Mayana Zatz Paulo A Otto

New York v.25, n.2 , p.219-31, 1986 American Journal of Medical Genetics

New York 1986

Item não circula. Consulte sua biblioteca.(Acessar)

4
Recognizing Ullrich-Turner syndrome by discriminant analysis of craniofacial structure
Recognizing Ullrich-Turner syndrome by discriminant analysis of craniofacial structure
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Recognizing Ullrich-Turner syndrome by discriminant analysis of craniofacial structure

Kaiser, Christiane ; Abt, Klaus

American journal of medical genetics, 1996-03, Vol.62 (2), p.113-119 [Periódico revisado por pares]

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

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5
Pedigree discriminant analysis: A method to identify monogenic segregation
Pedigree discriminant analysis: A method to identify monogenic segregation
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Pedigree discriminant analysis: A method to identify monogenic segregation

Zlotnik, L. H. ; Elston, R. C. ; Namboodiri, K. K.

American journal of medical genetics, 1983-06, Vol.15 (2), p.307-313 [Periódico revisado por pares]

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

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6
Improved detection of Duchenne muscular dystrophy heterozygotes using discriminant analysis of creatine kinase levels
Improved detection of Duchenne muscular dystrophy heterozygotes using discriminant analysis of creatine kinase levels
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Improved detection of Duchenne muscular dystrophy heterozygotes using discriminant analysis of creatine kinase levels

Muir, W. A. ; Knoke, J. ; Martin, A. ; Vignos, P. ; McErlean, A. ; Opitz, John M.

American journal of medical genetics, 1983-01, Vol.14 (1), p.125-134 [Periódico revisado por pares]

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

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7
Evaluation of carrier detection rates for duchenne and becker muscular dystrophies using serum creatine-kinase(CK) and pyruvate-kinase(PK) through discriminant analysis
Evaluation of carrier detection rates for duchenne and becker muscular dystrophies using serum creatine-kinase(CK) and pyruvate-kinase(PK) through discriminant analysis
Material Type:
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Evaluation of carrier detection rates for duchenne and becker muscular dystrophies using serum creatine-kinase(CK) and pyruvate-kinase(PK) through discriminant analysis

Zatz, Mayana ; Otto, Paulo A. ; Reynolds, James F.

American journal of medical genetics, 1986-10, Vol.25 (2), p.219-230 [Periódico revisado por pares]

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

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8
Waardenburg syndrome: Clinical differentiation between types I and II
Waardenburg syndrome: Clinical differentiation between types I and II
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Waardenburg syndrome: Clinical differentiation between types I and II

Pardono, Eliete ; van Bever, Yolande ; van den Ende, Jenneke ; Havrenne, Poti C. ; Iughetti, Paula ; Maestrelli, Sylvia R.P. ; Costa F, Orozimbo ; Richieri-Costa, Antonio ; Frota-Pessoa, Oswaldo ; Otto, Paulo A.

American journal of medical genetics, 2003-03, Vol.117A (3), p.223-235 [Periódico revisado por pares]

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

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9
Discriminant analysis of ribosomal protein synthesis findings in carrier detection of duchenne muscular dystrophy
Discriminant analysis of ribosomal protein synthesis findings in carrier detection of duchenne muscular dystrophy
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Discriminant analysis of ribosomal protein synthesis findings in carrier detection of duchenne muscular dystrophy

Ionasescu, V. ; Burmeister, L. ; Hanson, J.

American journal of medical genetics, 1980, Vol.5 (1), p.5-12 [Periódico revisado por pares]

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

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10
Metacarpophalangeal pattern profile analysis in Noonan syndrome
Metacarpophalangeal pattern profile analysis in Noonan syndrome
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Metacarpophalangeal pattern profile analysis in Noonan syndrome

Butler, Merlin G. ; Kumar, Robert ; Davis, Mende F. ; Gale, David D. ; Dahir, George A. ; Meaney, F. John

American journal of medical genetics, 2000-05, Vol.92 (2), p.128-131 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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Deste Autor:

  1. Zatz, M
  2. Otto, P

Neste Assunto:

  1. Humans
  2. Genetics & Heredity
  3. Life Sciences & Biomedicine
  4. Science & Technology
  5. Female

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