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R Laxova

Showing results (31-40 of 54) with videos related to

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American Journal of Human Genetics|August 1, 1986
Normal dosage of the insulin and insulin-like growth factor II genes in patients with the Beckwith-Wiedemann syndromeR A Spritz, D Mager, R M Pauli, et al.
Journal of Medical Genetics|June 1, 1971
A case of XYY Down's syndrome confirmed by autoradiographyR Laxova, J A McKeown, P Saldaña, et al.
Clinical Genetics|October 1, 1977
A family with syndactyly type II (synpolydactyly)M A Ridler, R Laxova, K Dewhurst, et al.
American Journal of Ophthalmology|July 15, 1987
Apparent Coats' disease and pericentric inversion of chromosome 3G L Skuta, T D France, T S Stevens, et al.
Archives of Disease in Childhood|March 1, 1973
Family with probable achondrogenesis and lipid inclusions in fibroblastsR Laxova, P T Ohara, M A Ridler, et al.
American Journal of Medical Genetics|November 15, 1992
Waardenburg syndrome type I in a child with deletion (2) (q35q36.2)S J Kirkpatrick, C M Kent, R Laxova, et al.
Genomics|April 1, 1991
Waisman syndrome, a human X-linked recessive basal ganglia disorder with mental retardation: localization to Xq27.3-qterR G Gregg, A B Metzenberg, K Hogan, et al.
American Journal of Medical Genetics|August 1, 1985
An X-linked recessive basal ganglia disorder with mental retardationR Laxova, E S Brown, K Hogan, et al.
American Journal of Medical Genetics|January 1, 1981
Idiopathic hydrops fetalis report of 4 patients including 2 affected sibsS M Schwartz, C Viseskul, R Laxova, et al.
American Journal of Medical Genetics|September 1, 1991
A 7-year old white-male boy with progressive neurological deteriorationL A Barness, K Henry, P Kling, et al.
Pageof 6

Showing results (31-40 of 54) with videos related to

Sort By:
Pageof 6
American Journal of Human Genetics|August 1, 1986
Normal dosage of the insulin and insulin-like growth factor II genes in patients with the Beckwith-Wiedemann syndromeR A Spritz, D Mager, R M Pauli, et al.
Journal of Medical Genetics|June 1, 1971
A case of XYY Down's syndrome confirmed by autoradiographyR Laxova, J A McKeown, P Saldaña, et al.
Clinical Genetics|October 1, 1977
A family with syndactyly type II (synpolydactyly)M A Ridler, R Laxova, K Dewhurst, et al.
American Journal of Ophthalmology|July 15, 1987
Apparent Coats' disease and pericentric inversion of chromosome 3G L Skuta, T D France, T S Stevens, et al.
Archives of Disease in Childhood|March 1, 1973
Family with probable achondrogenesis and lipid inclusions in fibroblastsR Laxova, P T Ohara, M A Ridler, et al.
American Journal of Medical Genetics|November 15, 1992
Waardenburg syndrome type I in a child with deletion (2) (q35q36.2)S J Kirkpatrick, C M Kent, R Laxova, et al.
Genomics|April 1, 1991
Waisman syndrome, a human X-linked recessive basal ganglia disorder with mental retardation: localization to Xq27.3-qterR G Gregg, A B Metzenberg, K Hogan, et al.
American Journal of Medical Genetics|August 1, 1985
An X-linked recessive basal ganglia disorder with mental retardationR Laxova, E S Brown, K Hogan, et al.
American Journal of Medical Genetics|January 1, 1981
Idiopathic hydrops fetalis report of 4 patients including 2 affected sibsS M Schwartz, C Viseskul, R Laxova, et al.
American Journal of Medical Genetics|September 1, 1991
A 7-year old white-male boy with progressive neurological deteriorationL A Barness, K Henry, P Kling, et al.
Pageof 6