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B Penchaszadeh

Showing results (21-30 of 37) with videos related to

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Journal of Medical Genetics|June 1, 1975
Trisomy 22. Two new cases and delineation of the phenotypeV B Penchaszadeh, R Coco
Journal De Genetique Humaine|March 1, 1977
Partial deficiency of long arm of chromosome No. 11R Coco, V B Penchaszadeh
Community Genetics|June 5, 2004
Genetic services to the latino population in the United StatesV B Penchaszadeh, D Puñales-Morejón
Community Genetics|November 16, 2004
Community genetic services in Latin America and regional network of medical genetics. Recommendations of a World Health Organization consultationSusana Kofman-Alfaro, Victor B Penchaszadeh
Genetics and Molecular Biology|April 26, 2014
Genetics and human rights. Two histories: Restoring genetic identity after forced disappearance and identity suppression in Argentina and after compulsory isolation for leprosy in BrazilVictor B Penchaszadeh, Lavinia Schuler-Faccini
American Journal of Medical Genetics|February 1, 1989
A new syndrome with distinct facial and auricular malformations and dominant inheritanceV Simosa, V B Penchaszadeh, T Bustos
American Journal of Medical Genetics|April 1, 1982
The nasopalpebral lipoma-coloboma syndrome: a new autosomal dominant dysplasia-malformation syndrome with congenital nasopalpebral lipomas, eyelid colobomas, telecanthus, and maxillary hypoplasiaV B Penchaszadeh, D Velasquez, R Arrivillaga
Journal of Medical Genetics|August 1, 1976
Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome: dominant inheritance and variable expressionV B Penchaszadeh, T C de Negrotti
Cancer Genetics and Cytogenetics|February 1, 1984
Chromosome fragility in patients with sporadic unilateral retinoblastomaM de Nuñez, V B Penchaszadeh, E Pimentel
Annales De Genetique|June 1, 1975
A case of ring 18 chromosome in a sibship with multiple spontaneous abortionsR Coco, C Z Barreiro, V B Penchaszadeh
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Journal of Medical Genetics|June 1, 1975
Trisomy 22. Two new cases and delineation of the phenotypeV B Penchaszadeh, R Coco
Journal De Genetique Humaine|March 1, 1977
Partial deficiency of long arm of chromosome No. 11R Coco, V B Penchaszadeh
Community Genetics|June 5, 2004
Genetic services to the latino population in the United StatesV B Penchaszadeh, D Puñales-Morejón
Community Genetics|November 16, 2004
Community genetic services in Latin America and regional network of medical genetics. Recommendations of a World Health Organization consultationSusana Kofman-Alfaro, Victor B Penchaszadeh
Genetics and Molecular Biology|April 26, 2014
Genetics and human rights. Two histories: Restoring genetic identity after forced disappearance and identity suppression in Argentina and after compulsory isolation for leprosy in BrazilVictor B Penchaszadeh, Lavinia Schuler-Faccini
American Journal of Medical Genetics|February 1, 1989
A new syndrome with distinct facial and auricular malformations and dominant inheritanceV Simosa, V B Penchaszadeh, T Bustos
American Journal of Medical Genetics|April 1, 1982
The nasopalpebral lipoma-coloboma syndrome: a new autosomal dominant dysplasia-malformation syndrome with congenital nasopalpebral lipomas, eyelid colobomas, telecanthus, and maxillary hypoplasiaV B Penchaszadeh, D Velasquez, R Arrivillaga
Journal of Medical Genetics|August 1, 1976
Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome: dominant inheritance and variable expressionV B Penchaszadeh, T C de Negrotti
Cancer Genetics and Cytogenetics|February 1, 1984
Chromosome fragility in patients with sporadic unilateral retinoblastomaM de Nuñez, V B Penchaszadeh, E Pimentel
Annales De Genetique|June 1, 1975
A case of ring 18 chromosome in a sibship with multiple spontaneous abortionsR Coco, C Z Barreiro, V B Penchaszadeh
Pageof 4