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Refinado por: Título de revista: American Journal of Medical Genetics. Part A eliminar
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1
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

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2
Single median maxillary central incisor, hypophyseal tumor, and SHH mutation
Single median maxillary central incisor, hypophyseal tumor, and SHH mutation
Material Type:
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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

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3
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:
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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

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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
Material Type:
Artículo 		Añadir a Mi Portal

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

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5
Single median maxillary central incisor, hypophyseal tumor, and SHH mutation
Single median maxillary central incisor, hypophyseal tumor, and SHH mutation
Material Type:
Artículo 		Añadir a Mi Portal

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

Comprobar fondos(Obténgalo)

6
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:
Artículo 		Añadir a Mi Portal

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

Comprobar fondos(Obténgalo)

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

Lucilene Arilho Ribeiro Rita de Cássia Mecca Guerini; Antonio Richieri-Costa

American Journal of Medical Genetics. Part A v. 136, n. 4, p. 350-351, Aug., 2005

Hoboken 2005

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8
Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects
Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects
Material Type:
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Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects

Lucilene Arilho Ribeiro Rita de Cássia Mecca Guerini; Antonio Richieri-Costa

American Journal of Medical Genetics. Part A v. 136, n. 4, p. 350-351, Aug., 2005

Hoboken 2005

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9
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
Material Type:
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Holoprosencephaly and holoprosencephaly-like phenotype and GAS1 DNA sequence changes report of four brazilian patients

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

American Journal of Medical Genetics, Part A Hoboken v. 152A, n. 7, p. 1688-1694, July 2010

Hoboken 2010

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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
Material Type:
Artículo 		Añadir a Mi Portal

Holoprosencephaly and holoprosencephaly-like phenotype and GAS1 DNA sequence changes report of four brazilian patients

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

American Journal of Medical Genetics, Part A Hoboken v. 152A, n. 7, p. 1688-1694, July 2010

Hoboken 2010

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por este autor/creador:

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

con este tema:

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

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