Z. Nazara

发表

A distinct osteochondrodysplasia with hypertrichosis—Individualization of a probable autosomal recessive entity

J. Śanchez-Corona, J. Cantú, A. Hernández, 2004, Human Genetics.

Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: further delineation of a new genetic syndrome.

J. Śanchez-Corona, J. Cantú, L. Figuera, 1997, American journal of medical genetics.

A distinct dysmorphic syndrome with congenital glaucoma and probable autosomal recessive inheritance.

J. Śanchez-Corona, J. Cantú, D. García-Cruz, 1990, Ophthalmic paediatrics and genetics.

Generalized osteoporosis in a patient with oculocutaneous hypopigmentation syndrome (OOCHS), without cerebral defects A new syndrome?

A. Hernández, M. C. Reynoso, L. Bobadilla, 1996, Clinical genetics.

Microcephaly, distinctive facies, single atrium, postaxial polydactyly, skeletal defects and mental retardation: a new familial faciocardiomelic syndrome?

J. Śanchez-Corona, J. García-Ortiz, D. García-Cruz, 2007, Clinical dysmorphology.

De novo dir dup (1)(q3200----4200) in an adult. Further delineation of the pure 1q trisomy syndrome.

J. Śanchez-Corona, P. Barros-Núñez, C. Medina, 1989, Annales de Genetique.

Aneuploidies, chromosome aberrations and dominant gene mutations detected in 113,913 consecutive newborn children in Mexico.

A. Hernández, M. C. Reynoso, A. Rolón, 1990, Mutation research.

De novo partial trisomy of chromosome 18(pter yields q11:). Some observations on the phenotype mapping of chromosome 18 imbalances.

J. Cantú, A. Hernández, B. Ibarra, 1979, Annales de genetique.

Frontonasal dysplasia in the Klippel‐Feil syndrome: A new associated malformation

J. Cantú, A. Hernández, R. Fragoso, 1982, Clinical genetics.

Simultaneous trisomy 10q24 leads to qter and monosomy 4p16: an example of epistasis at the chromosome level.

J. Śanchez-Corona, J. Cantú, H. Rivera, 1981, Annales de genetique.

On the deletion 4p16 Wolf-Hirschhorn syndrome.

J. Cantú, A. Hernández, A. Rolón, 1979, Annales de genetique.

Ehlers‐Danlos features with progeroid facies and mild mental retardation

J. Cantú, R. Fragoso, Z. Nazara, 1986, Clinical genetics.

A probably distinct autosomal recessive thoraco-limb dysplasia.

H. Rivera, Z. Nazara, M. L. Ramírez, 1988, Journal of medical genetics.

A probable monogenic form of polyostotic fibrous dysplasia

J. Cantú, A. Hernández, M. Alvarez-Arratia, 1983, Clinical genetics.

Type and contretype signs in monosomy and trisomy 9p. On a case 46,XY, del (9) (pter yields p12:).

J. Cantú, H. Rivera, A. Hernández, 1979, Annales de genetique.

Osteopoikilosis: report of a familial case.

J. Śanchez-Corona, D. García-Cruz, Z. Nazara, 1994, Genetic counseling.

Some clinical and cytogenetic observations on a ring chromosome 13 (p11 q34).

J. Śanchez-Corona, J. Cantú, H. Rivera, 1979, Annales de genetique.

Further clinical and radiological features in metaphyseal chondrodysplasia Jansen type.

J. Cantú, A. Hernández, G. Vaca, 1981, Radiology.

Individualization of a syndrome with mental deficiency, macrocranium, peculiar facies, and cardiac and skeletal anomalies

J. Śanchez-Corona, J. Cantú, Z. Nazara, 1982, Clinical genetics.

49,XXXXX syndrome.

J. Cantú, A. Hernández, R. Fragoso, 1982, Annales de genetique.

Autosomal dominant congenital macroglossia: further delineation of the syndrome.

A. Hernández, M. C. Reynoso, R. Fragoso, 1994, Genetic counseling.

Prenatal growth retardation, pelvic hypoplasia, and arthrogrypotic changes of lower limbs: a distinct autosomal-recessive disorder.

A. Hernández, M. C. Reynoso, Z. Nazara, 1998, American journal of medical genetics.

Guadalajara camptodactyly syndrome

J. Cantú, H. Rivera, A. Hernández, 1980, Clinical genetics.

Keratosis palmaris et plantaris with clinodactyly. A distinct autosomal dominant genodermatosis.

J. Cantú, A. González-mendoza, A. Hernández, 1981, Dermatologica.

Monosomy 20p due to a de novo del(20)(p12.2). Clinical and radiological delineation of the syndrome.

J. Śanchez-Corona, J. Cantú, H. Rivera, 1985, Annales de genetique.

Achalasia microcephaly syndrome in a patient with consanguineous parents: support for a.m. being a distinct autosomal recessive condition

M. C. Reynoso, R. Fragoso, Z. Nazara, 1989, Clinical genetics.