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J M Opitz

Clinical genetics

Showing results (1-10 of 7) with videos related to

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Clinical Genetics|May 1, 1975
Autosomal recessive syndrome of cerebellar ataxia and hypogonadotropic hypogonadismG Neuhäuser, J M Opitz
Clinical Genetics|March 1, 1976
Familial spastic paraplegia with distal muscle wasting in the Old Order Amish; atypical Troyer syndrome or "new" syndromeG Neuhäuser, C Wiffler, J M Opitz
Clinical Genetics|March 1, 1976
Autosomal recessive syndrome of pseudogliomantous blindness, osteoporosis and mild mental retardationG Neuhäuser, E G Kaveggia, J M Opitz
Clinical Genetics|May 1, 1975
The evaluation of infants with the Zellweger (cerebro-hepato-renal) syndromeK W Gilchrist, E F Gilbert, N T Shahidi, et al.
Clinical Genetics|November 1, 1976
Hypertrichosis lanuginosa in a mother and sonN Freire-Maia, J Felizali, A C de Figueiredo, et al.
Clinical Genetics|January 11, 1976
Essential tremor, nystagmus and duodenal ulceration. A "new" dominantly inherited conditionG Neuhäuser, R F Daly, N C Magnelli, et al.
Clinical Genetics|May 11, 1975
Familial Kallmann syndrome with unilateral renal aplasiaJ D Wegenke, D T Uehling, J B Wear, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Clinical Genetics|May 1, 1975
Autosomal recessive syndrome of cerebellar ataxia and hypogonadotropic hypogonadismG Neuhäuser, J M Opitz
Clinical Genetics|March 1, 1976
Familial spastic paraplegia with distal muscle wasting in the Old Order Amish; atypical Troyer syndrome or "new" syndromeG Neuhäuser, C Wiffler, J M Opitz
Clinical Genetics|March 1, 1976
Autosomal recessive syndrome of pseudogliomantous blindness, osteoporosis and mild mental retardationG Neuhäuser, E G Kaveggia, J M Opitz
Clinical Genetics|May 1, 1975
The evaluation of infants with the Zellweger (cerebro-hepato-renal) syndromeK W Gilchrist, E F Gilbert, N T Shahidi, et al.
Clinical Genetics|November 1, 1976
Hypertrichosis lanuginosa in a mother and sonN Freire-Maia, J Felizali, A C de Figueiredo, et al.
Clinical Genetics|January 11, 1976
Essential tremor, nystagmus and duodenal ulceration. A "new" dominantly inherited conditionG Neuhäuser, R F Daly, N C Magnelli, et al.
Clinical Genetics|May 11, 1975
Familial Kallmann syndrome with unilateral renal aplasiaJ D Wegenke, D T Uehling, J B Wear, et al.
Pageof 1