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American Journal of Medical Genetics
|
January 15, 1994
Newly recognized autosomal recessive faciothoracoskeletal syndrome
A Richieri-Costa, M L Guion-Almeida, J R Lauris, et al.
Birth Defects Original Article Series
|
January 1, 1996
Amniotic bands and the EEC syndrome
M L Guion-Almeida, E S Rodini, S C Pereira, et al.
American Journal of Medical Genetics
|
October 27, 1998
Smith-Fineman-Myers syndrome in apparently monozygotic twins
M L Guion-Almeida, A Tabith, N M Kokitsu-Nakata, et al.
American Journal of Medical Genetics
|
March 25, 1998
Blepharo-Cheilo-Dontic (BCD) syndrome: report on four new patients
M L Guion-Almeida, E S Rodini, N M Kokitsu-Nakata, et al.
American Journal of Medical Genetics
|
August 17, 1999
Auriculo-condylar syndrome: further evidence for a new disorder
M L Guion-Almeida, N M Kokitsu-Nakata, R M Zechi-Ceide, et al.
American Journal of Medical Genetics
|
July 1, 1993
Newly recognized blepharofacioskeletal syndrome
A Richieri-Costa, M L Guion-Almeida, E S Rodini, et al.
Journal of Pediatric Genetics
|
September 15, 2016
Clinical findings in children with congenital anomalies and misoprostol intrauterine exposure: a study of 38 cases
Siulan Vendramini-Pittoli, Maria L Guion-Almeida, Antonio Richieri-Costa, et al.
American Journal of Medical Genetics
|
July 1, 1993
Mandibulofacial dysostosis: report on two Brazilian families suggesting autosomal recessive inheritance
A Richieri-Costa, M A Bortolozo, J R Lauris, et al.
Clinical Genetics
|
June 26, 2002
Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome
P Sandrin-Garcia, C Macedo, L R Martelli, et al.
Clinical Dysmorphology
|
March 28, 2015
An unusual presentation of oculoauriculovertebral spectrum with a Tessier 30 cleft: report on two cases
Siulan Vendramini-Pittoli, Maria L Guion-Almeida, Juliana M Santos, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 55) with videos related to
Sort By:
Page
of 6
American Journal of Medical Genetics
|
January 15, 1994
Newly recognized autosomal recessive faciothoracoskeletal syndrome
A Richieri-Costa, M L Guion-Almeida, J R Lauris, et al.
Birth Defects Original Article Series
|
January 1, 1996
Amniotic bands and the EEC syndrome
M L Guion-Almeida, E S Rodini, S C Pereira, et al.
American Journal of Medical Genetics
|
October 27, 1998
Smith-Fineman-Myers syndrome in apparently monozygotic twins
M L Guion-Almeida, A Tabith, N M Kokitsu-Nakata, et al.
American Journal of Medical Genetics
|
March 25, 1998
Blepharo-Cheilo-Dontic (BCD) syndrome: report on four new patients
M L Guion-Almeida, E S Rodini, N M Kokitsu-Nakata, et al.
American Journal of Medical Genetics
|
August 17, 1999
Auriculo-condylar syndrome: further evidence for a new disorder
M L Guion-Almeida, N M Kokitsu-Nakata, R M Zechi-Ceide, et al.
American Journal of Medical Genetics
|
July 1, 1993
Newly recognized blepharofacioskeletal syndrome
A Richieri-Costa, M L Guion-Almeida, E S Rodini, et al.
Journal of Pediatric Genetics
|
September 15, 2016
Clinical findings in children with congenital anomalies and misoprostol intrauterine exposure: a study of 38 cases
Siulan Vendramini-Pittoli, Maria L Guion-Almeida, Antonio Richieri-Costa, et al.
American Journal of Medical Genetics
|
July 1, 1993
Mandibulofacial dysostosis: report on two Brazilian families suggesting autosomal recessive inheritance
A Richieri-Costa, M A Bortolozo, J R Lauris, et al.
Clinical Genetics
|
June 26, 2002
Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome
P Sandrin-Garcia, C Macedo, L R Martelli, et al.
Clinical Dysmorphology
|
March 28, 2015
An unusual presentation of oculoauriculovertebral spectrum with a Tessier 30 cleft: report on two cases
Siulan Vendramini-Pittoli, Maria L Guion-Almeida, Juliana M Santos, et al.
Page
of 6