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Unusual inheritance of Becker type muscular dystrophy

Journal of medical genetics, 1978-04, Vol.15 (2), p.116-118

1978

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Hypertrophic pyloric stenosis: adult and congenital types occurring in the same family

Journal of medical genetics, 1969-06, Vol.6 (2), p.126-128

1969

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Dyschondrosteosis. A Mexican family with two affected males

Clinical genetics, 1972-05, Vol.3 (3), p.154-157

1972

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Brachydactyly type B and symphalangism in different members of a Mexican family

Annales de génétique, 1975-06, Vol.18 (2), p.131

1975

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Duplication 11q and deletion 5p syndromes due to a reciprocal translocation segregating in four generations

American journal of medical genetics, 1988-01, Vol.29 (1), p.187-192

1988

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Rotor syndrome, a family study

Revista de investigacion clinica, 1974-10, Vol.26 (4), p.363

1974

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Supernumerary bisatellited chromosome in a family ascertained through a patient with Sturge-Weber syndrome

Annales de génétique, 1975-03, Vol.18 (1), p.45

1975

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Gerodermia osteodysplastica hereditaria: Report of three affected brothers and literature review

American journal of medical genetics, 1979, Vol.3 (4), p.389-395

1979

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A glucose 6-phosphate dehydrogenase Gd (-) Castilla variant characterized by mild deficiency associated with drug-induced hemolytic anemia

The Journal of laboratory and clinical medicine, 1977-10, Vol.90 (4), p.754

1977

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A new glucose-6-phosphate dehydrogenase variant, Gd(-) tepic, characterized by moderate enzyme deficiency and mild episodes of hemolytic anemia

Human genetics, 1985, Vol.69 (1), p.19-21

1985

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Hypochondroplasia. Study of four cases in two Mexican families (author's transl)

Revista de investigacion clinica, 1975-04, Vol.27 (2)

1975

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Multiple epiphyseal dysplasia tarda. A family with autosomal recessive inheritance

Clinical genetics, 1974-01, Vol.6 (1), p.15-19

1974

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Sensitivity of 6 genetic markers for the identification of illegitimacy in Mexico City

Revista de investigacion clinica, 1985-01, Vol.37 (1), p.27

1985

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Hereditary radioulnar sinostosis (author's transl)

Revista de investigacion clinica, 1978-07, Vol.30 (3), p.307

1978

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Cytogenetic studies in Fanconi's anemia. Description of a case with bone marrow clonal evolution

Clinical genetics, 1974-01, Vol.5 (1), p.72-76

1974

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Preliminary Draft of a Universal Declaration on the Human Genome and Human Rights

Politics and the life sciences, 1996-09, Vol.15 (2), p.332-334

International Bioethics Committee, UNESCO

1996

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Familial Mediterranean fever in Mexico City

Revista de investigacion clinica, 1986-10, Vol.38 (4), p.389

1986

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Hereditary and epidemiological aspects of erythrocyte glucose-6-phosphate dehydrogenase deficiency in Mexico

Gaceta médica de México, 1976-06, Vol.111 (6), p.454

1976

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Familial gastric cancer

Revista de investigacion clinica, 1987-10, Vol.39 (4), p.359

1987

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Albumin Mexico, a New Variant of Serum Albumin

Nature (London), 1967-09, Vol.215 (5107), p.1288-1289

1967

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E type brachydactyly in a Mexican family

Revista de investigacion clinica, 1970-01, Vol.22 (1), p.49

1970

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A new syndrome characterized by mental retardation, epilepsy, palpebral conjunctival telangiectasias and IgA deficiency

Clinical genetics, 1978-02, Vol.13 (2), p.154-158

1978

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Nemaline myopathy. A family suggestive of recessive inheritance (author's transl)

Revista de investigacion clinica, 1974-10, Vol.26 (4), p.373

1974

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Complex segregation analysis of diabetes mellitus

Human heredity, 1979-01, Vol.29 (6), p.325-333

1979

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Hereditary pancreatitis. Afamily with 4 affected members (author's transl)

Revista de investigacion clinica, 1977-04, Vol.29 (2), p.165

1977

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Unusual inheritance of Becker type muscular dystrophy

Hypertrophic pyloric stenosis: adult and congenital types occurring in the same family

Dyschondrosteosis. A Mexican family with two affected males

Brachydactyly type B and symphalangism in different members of a Mexican family

Duplication 11q and deletion 5p syndromes due to a reciprocal translocation segregating in four generations

Rotor syndrome, a family study

Supernumerary bisatellited chromosome in a family ascertained through a patient with Sturge-Weber syndrome

Gerodermia osteodysplastica hereditaria: Report of three affected brothers and literature review

A glucose 6-phosphate dehydrogenase Gd (-) Castilla variant characterized by mild deficiency associated with drug-induced hemolytic anemia

A new glucose-6-phosphate dehydrogenase variant, Gd(-) tepic, characterized by moderate enzyme deficiency and mild episodes of hemolytic anemia

Hypochondroplasia. Study of four cases in two Mexican families (author's transl)

Multiple epiphyseal dysplasia tarda. A family with autosomal recessive inheritance

Sensitivity of 6 genetic markers for the identification of illegitimacy in Mexico City

Hereditary radioulnar sinostosis (author's transl)

Cytogenetic studies in Fanconi's anemia. Description of a case with bone marrow clonal evolution

Preliminary Draft of a Universal Declaration on the Human Genome and Human Rights

Familial Mediterranean fever in Mexico City

Hereditary and epidemiological aspects of erythrocyte glucose-6-phosphate dehydrogenase deficiency in Mexico

Familial gastric cancer

Albumin Mexico, a New Variant of Serum Albumin

E type brachydactyly in a Mexican family

A new syndrome characterized by mental retardation, epilepsy, palpebral conjunctival telangiectasias and IgA deficiency

Nemaline myopathy. A family suggestive of recessive inheritance (author's transl)

Complex segregation analysis of diabetes mellitus

Hereditary pancreatitis. Afamily with 4 affected members (author's transl)

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