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P A Otto

Showing results (11-20 of 57) with videos related to

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American Journal of Medical Genetics|April 1, 1992
Notes on the population genetics of fragile X syndromeA M Vianna-Morgante, P A Otto
American Journal of Medical Genetics|September 1, 1985
Serum CK-MB activity in progressive muscular dystrophy: is it of nosologic value?M Vainzof, M Zatz, P A Otto
Journal of Medical Genetics|June 1, 1976
X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with XgM Zatz, C Penha-Serrano, P A Otto
Chromosoma|January 1, 1981
The behavior of allocyclic chromosomes in Bloom's syndromeP G Otto, P A Otto, E Therman
Human Heredity|January 1, 1989
Estimates of conditional heterozygosity risks for young females in Duchenne muscular dystrophyM R Passos-Bueno, P A Otto, M Zata
American Journal of Medical Genetics|November 14, 2000
Calculation of recurrence risks for heterogeneous genetic disordersM C Braga, P A Otto, O Frota-Pessoa
Heredity|April 1, 1990
Allele frequency estimates when only heterozygotes can be recognized: method of estimation and application in the case of chromosomal inversion polymorphisms in DrosophilaL B Klaczko, P A Otto, A A Peixoto
American Journal of Medical Genetics|August 1, 1985
Unusual type of brachydactyly associated with short stature and facial anomalies. A new syndrome?A Richieri-Costa, G M Colletto, P A Otto
The Journal of Heredity|July 1, 1976
The variation of recurrence risks with penetrance for isolated cases of autosomal dominant conditionsO Frota-Pessoa, P A Otto, J R Plaza
American Journal of Medical Genetics|April 1, 1988
Relationship between Mayer-Rokitansky-Küster (MRK) anomaly and hereditary renal adysplasia (HRA)R de C Pavanello, A Eigier, P A Otto
Pageof 6

Showing results (11-20 of 57) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics|April 1, 1992
Notes on the population genetics of fragile X syndromeA M Vianna-Morgante, P A Otto
American Journal of Medical Genetics|September 1, 1985
Serum CK-MB activity in progressive muscular dystrophy: is it of nosologic value?M Vainzof, M Zatz, P A Otto
Journal of Medical Genetics|June 1, 1976
X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with XgM Zatz, C Penha-Serrano, P A Otto
Chromosoma|January 1, 1981
The behavior of allocyclic chromosomes in Bloom's syndromeP G Otto, P A Otto, E Therman
Human Heredity|January 1, 1989
Estimates of conditional heterozygosity risks for young females in Duchenne muscular dystrophyM R Passos-Bueno, P A Otto, M Zata
American Journal of Medical Genetics|November 14, 2000
Calculation of recurrence risks for heterogeneous genetic disordersM C Braga, P A Otto, O Frota-Pessoa
Heredity|April 1, 1990
Allele frequency estimates when only heterozygotes can be recognized: method of estimation and application in the case of chromosomal inversion polymorphisms in DrosophilaL B Klaczko, P A Otto, A A Peixoto
American Journal of Medical Genetics|August 1, 1985
Unusual type of brachydactyly associated with short stature and facial anomalies. A new syndrome?A Richieri-Costa, G M Colletto, P A Otto
The Journal of Heredity|July 1, 1976
The variation of recurrence risks with penetrance for isolated cases of autosomal dominant conditionsO Frota-Pessoa, P A Otto, J R Plaza
American Journal of Medical Genetics|April 1, 1988
Relationship between Mayer-Rokitansky-Küster (MRK) anomaly and hereditary renal adysplasia (HRA)R de C Pavanello, A Eigier, P A Otto
Pageof 6