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1
Brief clinical report sporadic, idiopathic MCA/MR syndrome with the tibial aplasia/femoral bifurcation field defect
Brief clinical report sporadic, idiopathic MCA/MR syndrome with the tibial aplasia/femoral bifurcation field defect
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Brief clinical report sporadic, idiopathic MCA/MR syndrome with the tibial aplasia/femoral bifurcation field defect

Antonio Richieri-Costa Yolande van Bever

Revista Brasileira de Genética v. 14, n. 2, p. 563-568, June, 1991

Ribeirão Preto 1991

Item não circula. Consulte sua biblioteca.(Acessar)

2
Tibial hemimelia-split hand/foot syndrome, report of a brazilian family
Tibial hemimelia-split hand/foot syndrome, report of a brazilian family
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Tibial hemimelia-split hand/foot syndrome, report of a brazilian family

Antonio Richieri-Costa

Revista Brasileira de Genética v. 11, n. 4, p. 1009-1016, 1988

Ribeirão Preto 1988

Item não circula. Consulte sua biblioteca.(Acessar)

3
Tibial hemimelia report of a new brazilian family an overview
Tibial hemimelia report of a new brazilian family an overview
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Tibial hemimelia report of a new brazilian family an overview

Antonio Richieri-Costa

Revista Brasileira de Genética v. 13, n. 3, p. 613-623, Sept., 1990

Ribeirão Preto 1990

Item não circula. Consulte sua biblioteca.(Acessar)

4
Aural atresia, microtia, complex heart defect, and hearing loss syndrome additional case [Research Letter]
Aural atresia, microtia, complex heart defect, and hearing loss syndrome additional case [Research Letter]
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Aural atresia, microtia, complex heart defect, and hearing loss syndrome additional case [Research Letter]

Maria Leine Guion-Almeida Nancy Mizue Kokitsu Nakata

American Journal of Medical Genetics v. 117, n. 1, p. 84-83, Feb., 2003

New York 2003

Item não circula. Consulte sua biblioteca.(Acessar)

5
Aural atresia and microtia in Kabuki syndrome [Research Letter]
Aural atresia and microtia in Kabuki syndrome [Research Letter]
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Aural atresia and microtia in Kabuki syndrome [Research Letter]

Nancy Mizue Kokitsu Nakata Maria Leine Guion-Almeida

American Journal of Medical Genetics v. 118A, n. 4, p. 391-393, May, 2003

New York 2003

Item não circula. Consulte sua biblioteca.(Acessar)

6
Guadalajara camptodactyly syndrome type I report on a new case
Guadalajara camptodactyly syndrome type I report on a new case
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Guadalajara camptodactyly syndrome type I report on a new case

Roseli Maria Zechi Ceide Maria Leine Guion-Almeida; Antonio Richieri-Costa

Clinical Dysmorphology London v. 11, n. 2, p. 129-132, Apr. 2002

London 2002

Item não circula. Consulte sua biblioteca.(Acessar)

7
Conjoined twins report of a Brazilian twin belonging to the category duplicatas incompleta, an atypical parasite twinning type
Conjoined twins report of a Brazilian twin belonging to the category duplicatas incompleta, an atypical parasite twinning type
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Conjoined twins report of a Brazilian twin belonging to the category duplicatas incompleta, an atypical parasite twinning type

Antonio Richieri-Costa Maria Leine Guion-Almeida; Ulisses Frederigue Junior

Birth Defects Original Article Series New York v. 29, n. 1, p. 273-277, 1993

New York 1993

Item não circula. Consulte sua biblioteca.(Acessar)

8
The syndrome of frontonasal dysplasia, callosal agenesis, basal encephalocele, and eye anomalies phenotypic and aetiological considerations
The syndrome of frontonasal dysplasia, callosal agenesis, basal encephalocele, and eye anomalies phenotypic and aetiological considerations
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The syndrome of frontonasal dysplasia, callosal agenesis, basal encephalocele, and eye anomalies phenotypic and aetiological considerations

Antonio Richieri-Costa Maria Leine Guion-Almeida

International Journal of Medical Sciences v. 1, n. 1, p. 34-42, 2004

2004

Item não circula. Consulte sua biblioteca.(Acessar)

9
Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome?
Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome?
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Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome?

Maria Leine Guion-Almeida Ligiane Alves Machado Paula; Antonio Richieri-Costa

American Journal of Medical Genetics v. 129A, n. 2, p. 156-161, Aug., 2004

New York 2004

Item não circula. Consulte sua biblioteca.(Acessar)

10
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)

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