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D García-Cruz

Showing results (1-10 of 54) with videos related to

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Human Genetics|November 1, 1979
Heterozygous expression in 3-M slender-boned nanismD García-Cruz, J M Cantú
Human Genetics|January 19, 1978
Autosomal recessive sensorineural-conductive deafness, mental retardation, and pinna anomaliesJ M Cantú, R Ruenes, D García-Cruz
Annales De Genetique|January 5, 2002
Further clinical delineation in trisomy 1q32 syndromeI Nuño-Arana, J R González-García, D García-Cruz
Archives of Medical Research|January 1, 1995
Omphalocele-exstrophy-imperforate-anus-spina bifida (OEIS) complex in a male prenatally exposed to diazepamL A Lizcano-Gil, D García-Cruz, J Sánchez-Corona
Neurologia (Barcelona, Spain)|August 26, 2015
Ethical considerations in presymptomatic diagnosis of autosomal dominant spinocerebellar ataxiasM H Orozco-Gutiérrez, I Cervantes-Aragón, D García-Cruz
Human Genetics|January 1, 1980
Severe mental deficiency, proportionate dwarfism, and delayed sexual maturation. A distinct inherited syndromeJ M Cantú, J Sánchez-Corona, D García-Cruz, et al.
American Journal of Medical Genetics|July 9, 1999
Neocentromere at 13q32 in one of two stable markers derived from a 13q21 breakH Rivera, A I Vasquez, D García-Cruz, et al.
Birth Defects Original Article Series|January 1, 1977
A distinct skeletal dysplasia in an infant from consanguineous parentsJ M Cantú, C Manzano, P Pagán, et al.
Clinical Genetics|October 1, 1995
Spondylo-camptodactyly syndrome: a distinct autosomal dominant entity?L A Lizcano-Gil, D García-Cruz, J Sánchez-Corona, et al.
Human Genetics|January 1, 1984
Pure monosomy and trisomy 2q24.2----q3105 due to an inv ins(7;2)(q21.2;q3105q24.2) segregating in four generationsM Moller, D García-Cruz, H Rivera, et al.
Pageof 6

Showing results (1-10 of 54) with videos related to

Sort By:
Pageof 6
Human Genetics|November 1, 1979
Heterozygous expression in 3-M slender-boned nanismD García-Cruz, J M Cantú
Human Genetics|January 19, 1978
Autosomal recessive sensorineural-conductive deafness, mental retardation, and pinna anomaliesJ M Cantú, R Ruenes, D García-Cruz
Annales De Genetique|January 5, 2002
Further clinical delineation in trisomy 1q32 syndromeI Nuño-Arana, J R González-García, D García-Cruz
Archives of Medical Research|January 1, 1995
Omphalocele-exstrophy-imperforate-anus-spina bifida (OEIS) complex in a male prenatally exposed to diazepamL A Lizcano-Gil, D García-Cruz, J Sánchez-Corona
Neurologia (Barcelona, Spain)|August 26, 2015
Ethical considerations in presymptomatic diagnosis of autosomal dominant spinocerebellar ataxiasM H Orozco-Gutiérrez, I Cervantes-Aragón, D García-Cruz
Human Genetics|January 1, 1980
Severe mental deficiency, proportionate dwarfism, and delayed sexual maturation. A distinct inherited syndromeJ M Cantú, J Sánchez-Corona, D García-Cruz, et al.
American Journal of Medical Genetics|July 9, 1999
Neocentromere at 13q32 in one of two stable markers derived from a 13q21 breakH Rivera, A I Vasquez, D García-Cruz, et al.
Birth Defects Original Article Series|January 1, 1977
A distinct skeletal dysplasia in an infant from consanguineous parentsJ M Cantú, C Manzano, P Pagán, et al.
Clinical Genetics|October 1, 1995
Spondylo-camptodactyly syndrome: a distinct autosomal dominant entity?L A Lizcano-Gil, D García-Cruz, J Sánchez-Corona, et al.
Human Genetics|January 1, 1984
Pure monosomy and trisomy 2q24.2----q3105 due to an inv ins(7;2)(q21.2;q3105q24.2) segregating in four generationsM Moller, D García-Cruz, H Rivera, et al.
Pageof 6