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M C Reynoso

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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.
Ear, Nose, & Throat Journal|February 1, 1995
Autosomal dominant macroglossia: an addendum to the etiological classificationR Martinez y Martinez, M C Reynoso, A Hernandez, 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.
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.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Autosomal dominant congenital epiphyseal dysplasia limited to the femoral headsA Hernández, Z Nazara, M C Reynoso, et al.
Human Genetics|October 1, 1986
Autosomal dominant macroglossia in two unrelated familiesM C Reynoso, A Hernández, F Soto, et al.
Mutation Research|September 1, 1990
Aneuploidies, chromosome aberrations and dominant gene mutations detected in 113,913 consecutive newborn children in MexicoA Hernández, M C Reynoso, F Soto, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Autosomal dominant congenital macroglossia: further delineation of the syndromeM C Reynoso, A Hernández, L A Lizcano-Gil, et al.
Ophthalmic Paediatrics and Genetics|August 1, 1986
Ciliary and superciliary hypotrichosis. A distinct autosomal dominant traitL García-Esquivel, A Hernández, M C Reynoso, et al.
Clinical Genetics|September 1, 1985
Cortical blindness, growth and psychomotor retardation and postaxial polydactyly: a probably distinct autosomal recessive syndromeA Hernández, L García-Esquivel, M C Reynoso, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
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.
Ear, Nose, & Throat Journal|February 1, 1995
Autosomal dominant macroglossia: an addendum to the etiological classificationR Martinez y Martinez, M C Reynoso, A Hernandez, 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.
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.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Autosomal dominant congenital epiphyseal dysplasia limited to the femoral headsA Hernández, Z Nazara, M C Reynoso, et al.
Human Genetics|October 1, 1986
Autosomal dominant macroglossia in two unrelated familiesM C Reynoso, A Hernández, F Soto, et al.
Mutation Research|September 1, 1990
Aneuploidies, chromosome aberrations and dominant gene mutations detected in 113,913 consecutive newborn children in MexicoA Hernández, M C Reynoso, F Soto, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Autosomal dominant congenital macroglossia: further delineation of the syndromeM C Reynoso, A Hernández, L A Lizcano-Gil, et al.
Ophthalmic Paediatrics and Genetics|August 1, 1986
Ciliary and superciliary hypotrichosis. A distinct autosomal dominant traitL García-Esquivel, A Hernández, M C Reynoso, et al.
Clinical Genetics|September 1, 1985
Cortical blindness, growth and psychomotor retardation and postaxial polydactyly: a probably distinct autosomal recessive syndromeA Hernández, L García-Esquivel, M C Reynoso, et al.
Pageof 2