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M Opitz

Showing results (421-430 of 520) with videos related to

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American Journal of Medical Genetics. Part A|February 5, 2008
X-linked congenital ataxia: a new locus maps to Xq25-q27.1Ginevra Zanni, Enrico Bertini, Cecelia Bellcross, et al.
European Journal of Pediatrics|September 1, 1976
Chondrodysplasia punctata--rhizomelic form. Pathologic and radiologic studies of three infantsE F Gilbert, J M Opitz, J W Spranger, et al.
American Journal of Medical Genetics. Part A|May 20, 2011
A deletion 13q34/duplication 14q32.2-14q32.33 syndrome diagnosed 50 years after neonatal presentation as infantile hypercalcemiaPhilip D Pallister, Adam B Pallister, Sarah South, et al.
American Journal of Medical Genetics|December 8, 1998
Previously undescribed syndrome of spondylometaphyseal dysplasia, osteocartilaginous metaplasia of long bones, and progressive osteolysis of distal phalangesW R Osebold, A K Poznanski, J M Opitz, et al.
American Journal of Medical Genetics. Part A|May 8, 2013
Elements of morphology: standard terminology for the external genitaliaRaoul C M Hennekam, Judith E Allanson, Leslie G Biesecker, et al.
La Presse Medicale|May 22, 1971
[The campomelic syndrome]P Maroteaux, J Spranger, J M Opitz, et al.
European Journal of Pediatrics|April 6, 1976
Studies of malformation syndromes of man XXXXI B: nosologic studies in the Hanhart and the Möbius syndromeJ Herrmann, P D Pallister, E F Gilbert, et al.
Neuropadiatrie|July 1, 1971
Neurologic and psychometric findings in the Brachmann-De Lange syndromeA N Barr, J D Grabow, C G Matthews, et al.
American Journal of Medical Genetics|January 1, 1982
Clinicopathologic conference: a six-month-old infant with sudden onset of metabolic acidosis and shockM L Katcher, W E Segar, J J Wolfson, et al.
Journal of Medical Genetics|September 1, 1975
A syndrome of hypohidrotic ectodermal dysplasia with normal teeth, peculiar facies, pigmentary disturbances, psychomotor and growth retardation, bilateral nuclear cataract, and other signsN Freire-Maia, V A Fortes, L C Pereira, et al.
Pageof 52

Showing results (421-430 of 520) with videos related to

Sort By:
Pageof 52
American Journal of Medical Genetics. Part A|February 5, 2008
X-linked congenital ataxia: a new locus maps to Xq25-q27.1Ginevra Zanni, Enrico Bertini, Cecelia Bellcross, et al.
European Journal of Pediatrics|September 1, 1976
Chondrodysplasia punctata--rhizomelic form. Pathologic and radiologic studies of three infantsE F Gilbert, J M Opitz, J W Spranger, et al.
American Journal of Medical Genetics. Part A|May 20, 2011
A deletion 13q34/duplication 14q32.2-14q32.33 syndrome diagnosed 50 years after neonatal presentation as infantile hypercalcemiaPhilip D Pallister, Adam B Pallister, Sarah South, et al.
American Journal of Medical Genetics|December 8, 1998
Previously undescribed syndrome of spondylometaphyseal dysplasia, osteocartilaginous metaplasia of long bones, and progressive osteolysis of distal phalangesW R Osebold, A K Poznanski, J M Opitz, et al.
American Journal of Medical Genetics. Part A|May 8, 2013
Elements of morphology: standard terminology for the external genitaliaRaoul C M Hennekam, Judith E Allanson, Leslie G Biesecker, et al.
La Presse Medicale|May 22, 1971
[The campomelic syndrome]P Maroteaux, J Spranger, J M Opitz, et al.
European Journal of Pediatrics|April 6, 1976
Studies of malformation syndromes of man XXXXI B: nosologic studies in the Hanhart and the Möbius syndromeJ Herrmann, P D Pallister, E F Gilbert, et al.
Neuropadiatrie|July 1, 1971
Neurologic and psychometric findings in the Brachmann-De Lange syndromeA N Barr, J D Grabow, C G Matthews, et al.
American Journal of Medical Genetics|January 1, 1982
Clinicopathologic conference: a six-month-old infant with sudden onset of metabolic acidosis and shockM L Katcher, W E Segar, J J Wolfson, et al.
Journal of Medical Genetics|September 1, 1975
A syndrome of hypohidrotic ectodermal dysplasia with normal teeth, peculiar facies, pigmentary disturbances, psychomotor and growth retardation, bilateral nuclear cataract, and other signsN Freire-Maia, V A Fortes, L C Pereira, et al.
Pageof 52