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Refinado por: Nome da Publicação: American Journal Of Medical Genetics. Part A remover
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1
Single median maxillary central incisor, hypophyseal tumor, and SHH mutation
Single median maxillary central incisor, hypophyseal tumor, and SHH mutation
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Single median maxillary central incisor, hypophyseal tumor, and SHH mutation

Ribeiro, Lucilene Arilho ; Richieri-Costa, Antonio

American journal of medical genetics. Part A, 2005-08, Vol.136A (4), p.346-347 [Periódico revisado por pares]

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

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2
Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation
Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation
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Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation

Lucilene Arilho Ribeiro Antonio Richieri-Costa

American Journal of Medical Genetics. Part A v. 136, n. 4, p. 348-349, Aug., 2005

Hoboken 2005

Item não circula. Consulte sua biblioteca.(Acessar)

3
Single median maxillary central incisor, hypophyseal tumor, and SHH mutation
Single median maxillary central incisor, hypophyseal tumor, and SHH mutation
Material Type:
Artigo 		Adicionar ao Meu Espaço

Single median maxillary central incisor, hypophyseal tumor, and SHH mutation

Lucilene Arilho Ribeiro Antonio Richieri-Costa

American Journal of Medical Genetics. Part A v. 136, n. 4, p. 346-347, Aug., 2005

Hoboken 2005

Item não circula. Consulte sua biblioteca.(Acessar)

4
Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum new case and imaging review of previous cases
Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum new case and imaging review of previous cases
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Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum new case and imaging review of previous cases

Antonio Richieri-Costa Lucilene Arilho Ribeiro

American Journal of Medical Genetics. Part A v. 136, n. 4, p. 352-353, Aug., 2005

Hoboken 2005

Item não circula. Consulte sua biblioteca.(Acessar)

5
Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation
Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation
Material Type:
Artigo 		Adicionar ao Meu Espaço

Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation

Ribeiro, Lucilene Arilho ; Richieri-Costa, Antonio

American journal of medical genetics. Part A, 2005-08, Vol.136A (4), p.348-349 [Periódico revisado por pares]

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

Texto completo disponível

Citações Citado por
6
Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: New case and imaging review of previous cases
Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: New case and imaging review of previous cases
Material Type:
Artigo 		Adicionar ao Meu Espaço

Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: New case and imaging review of previous cases

Richieri-Costa, Antonio ; Ribeiro, Lucilene Arilho

American journal of medical genetics. Part A, 2005-08, Vol.136A (4), p.352-353 [Periódico revisado por pares]

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

Texto completo disponível

Citações Citado por
7
Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects
Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects
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Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects

Ribeiro, Lucilene Arilho ; Guerini, Rita de Cássia M. ; Richieri-Costa, Antonio

American journal of medical genetics. Part A, 2005-08, Vol.136A (4), p.350-351 [Periódico revisado por pares]

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

Texto completo disponível

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8
Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses
Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses
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Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses

Villela, Darine ; Mazzonetto, Patricia C. ; Migliavacca, Michele P. ; Perrone, Eduardo ; Guida, Gustavo ; Milanezi, Maria Fernanda G. ; Jorge, Alexander A. L. ; Ribeiro‐Bicudo, Lucilene A. ; Kok, Fernando ; Campagnari, Francine ; Rosso‐Giuliani, Liane ; Costa, Silvia Souza ; Vianna‐Morgante, Angela M. ; Pearson, Peter L. ; Krepischi, Ana C. V. ; Rosenberg, Carla

American journal of medical genetics. Part A, 2021-08, Vol.185 (8), p.2335-2344 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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9
The phenotypic spectrum of congenital Zika syndrome
The phenotypic spectrum of congenital Zika syndrome
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The phenotypic spectrum of congenital Zika syndrome

del Campo, Miguel ; Feitosa, Ian M. L. ; Ribeiro, Erlane M. ; Horovitz, Dafne D. G. ; Pessoa, André L. S. ; França, Giovanny V. A. ; García‐Alix, Alfredo ; Doriqui, Maria J. R. ; Wanderley, Hector Y. C. ; Sanseverino, Maria V. T. ; Neri, João I. C. F. ; Pina‐Neto, João M. ; Santos, Emerson S. ; Verçosa, Islane ; Cernach, Mirlene C. S. P. ; Medeiros, Paula F. V. ; Kerbage, Saile C. ; Silva, André A. ; van der Linden, Vanessa ; Martelli, Celina M. T. ; Cordeiro, Marli T. ; Dhalia, Rafael ; Vianna, Fernanda S. L. ; Victora, Cesar G. ; Cavalcanti, Denise P. ; Schuler‐Faccini, Lavinia

American journal of medical genetics. Part A, 2017-04, Vol.173 (4), p.841-857 [Periódico revisado por pares]

United States: Wiley Subscription Services, Inc

Texto completo disponível

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10
Holoprosencephaly and holoprosencephaly-like phenotype and GAS1 DNA sequence changes: Report of four Brazilian patients
Holoprosencephaly and holoprosencephaly-like phenotype and GAS1 DNA sequence changes: Report of four Brazilian patients
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Holoprosencephaly and holoprosencephaly-like phenotype and GAS1 DNA sequence changes: Report of four Brazilian patients

Ribeiro, Lucilene Arilho ; Quiezi, Rodrigo Gonçalves ; Nascimento, Adriana ; Bertolacini, Claudia Pereira ; Richieri-Costa, Antonio

American journal of medical genetics. Part A, 2010-07, Vol.152A (7), p.1688-1694 [Periódico revisado por pares]

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

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Deste Autor:

  1. Richieri-Costa, A
  2. Ribeiro, L
  3. Bertolacini, C
  4. Giugliani, R
  5. Zechi-Ceide, R

Neste Assunto:

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

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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