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Z Nazará

Showing results (1-10 of 31) with videos related to

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Radiology|July 1, 1979
Cleidocranial dysplasiaZ Nazará, R Fragoso, A Hernández, et al.
Human Genetics|April 5, 1979
Autosomal dominant acrodysostosisJ M Cantú, A Hernández, A Panduro-Cerda, et al.
American Journal of Medical Genetics|March 7, 1998
Prenatal growth retardation, pelvic hypoplasia, and arthrogrypotic changes of lower limbs: a distinct autosomal-recessive disorderA Sarralde, M C Reynoso, Z Nazará, et al.
Boletin Medico Del Hospital Infantil De Mexico|April 1, 1982
[Faciodigitogenital (Aarskog-Scott) syndrome]R Fragoso, D García-Cruz, J Sánchez-Corona, et al.
Clinical Genetics|November 1, 1982
Frontonasal dysplasia in the Klippel-Feil syndrome: a new associated malformationR Fragoso, A Cid-García, A Hernández, et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion|July 1, 1974
[Facioacromelic disostosis with metal retardation (author's transl)]J M Cantú, A Hernández, Z Nazará-Cazorla, et al.
Clinical Genetics|December 1, 1989
Achalasia microcephaly syndrome in a patient with consanguineous parents: support for a.m. being a distinct autosomal recessive conditionA Hernández, M C Reynoso, F Soto, et al.
Boletin Medico Del Hospital Infantil De Mexico|January 1, 1982
[Tricho-oculo-dentomandibular progeroid syndrome]A Hernández, C Martínez-Basalo, Z Nazará, et al.
Clinical Genetics|January 1, 1996
Generalized osteoporosis in a patient with oculocutaneous hypopigmentation syndrome (OOCHS), without cerebral defects. A new syndrome?A Hernández, Z Nazará, M C Reynoso, et al.
Clinical Genetics|October 1, 1982
Individualization of a syndrome with mental deficiency, macrocranium, peculiar facies, and cardiac and skeletal anomaliesJ M Cantú, J Sánchez-Corona, A Hernándes, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Radiology|July 1, 1979
Cleidocranial dysplasiaZ Nazará, R Fragoso, A Hernández, et al.
Human Genetics|April 5, 1979
Autosomal dominant acrodysostosisJ M Cantú, A Hernández, A Panduro-Cerda, et al.
American Journal of Medical Genetics|March 7, 1998
Prenatal growth retardation, pelvic hypoplasia, and arthrogrypotic changes of lower limbs: a distinct autosomal-recessive disorderA Sarralde, M C Reynoso, Z Nazará, et al.
Boletin Medico Del Hospital Infantil De Mexico|April 1, 1982
[Faciodigitogenital (Aarskog-Scott) syndrome]R Fragoso, D García-Cruz, J Sánchez-Corona, et al.
Clinical Genetics|November 1, 1982
Frontonasal dysplasia in the Klippel-Feil syndrome: a new associated malformationR Fragoso, A Cid-García, A Hernández, et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion|July 1, 1974
[Facioacromelic disostosis with metal retardation (author's transl)]J M Cantú, A Hernández, Z Nazará-Cazorla, et al.
Clinical Genetics|December 1, 1989
Achalasia microcephaly syndrome in a patient with consanguineous parents: support for a.m. being a distinct autosomal recessive conditionA Hernández, M C Reynoso, F Soto, et al.
Boletin Medico Del Hospital Infantil De Mexico|January 1, 1982
[Tricho-oculo-dentomandibular progeroid syndrome]A Hernández, C Martínez-Basalo, Z Nazará, et al.
Clinical Genetics|January 1, 1996
Generalized osteoporosis in a patient with oculocutaneous hypopigmentation syndrome (OOCHS), without cerebral defects. A new syndrome?A Hernández, Z Nazará, M C Reynoso, et al.
Clinical Genetics|October 1, 1982
Individualization of a syndrome with mental deficiency, macrocranium, peculiar facies, and cardiac and skeletal anomaliesJ M Cantú, J Sánchez-Corona, A Hernándes, et al.
Pageof 4