Diagnostic criteria for Walker-Warburg syndrome von Dobyns, William B., Pagon, Roberta A., Armstrong, Dawna, Curry, Cynthia J. R., Greenberg, Frank, Grix, Arthur, Holmes, Lewis B., Laxova, Renata, Michels, Virginia V., Robinow, Meinhard, Zimmerman, Roberta L., Opitz, John M., Reynolds, James F.

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Female pseudohermaphroditism with associated anomalies von Robinow, Meinhard

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Rickets, deficiency of alkaline phosphatase activity and premature loss of teeth in childhood von SOBEL, E H, CLARK, Jr, L C, FOX, R P, ROBINOW, M

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Mental retardation in Duchenne muscular dystrophy: Its relation to the maternal carrier state von Robinow, Meinhard

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Correspondence von Robinow, Meinhard

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The Variability of Weight and Height Increments from Birth to Six Years von Robinow, Meinhard

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Imperforate anus in the Pallister-Killian syndrome von Robinow, Meinhard

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Living history-autobiography: Pediatric genetics in a new world von Robinow, Meinhard

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Coarctation of the aorta inherited as an autosomal dominant trait von Beekman, Robert H., Robinow, Meinhard

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Respiratory obstruction and cor pulmonale in the Hallermann-Streiff syndrome von Robinow, Meinhard

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Care of Infants with Myelomeningocele von ROBINOW, MEINHARD, PINA, GLORIA, TURK, MARGARET A.

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Peromelia, ipsilateral subclavian atresia, coarctation, and aneurysms of the aorta resulting from intrauterine vascular occlusion von Robinow, Meinhard, Schatzman, Earl R., Oberheu, Kenneth

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THE STATISTICAL DIAGNOSIS OF ZYGOSITY IN MULTIPLE HUMAN BIRTHS von ROBINOW, MEINHARD

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In defense of chaos von Robinow, Meinhard, Shaw, Anthony

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Distal phalangeal hypoplasia and fingertip arches von Robinow, Meinhard, Johnson, G.F.

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Comment on COVESDEM syndrome von Robinow, Meinhard

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New syndrome von Robinow, Meinhard, Beemer, Frits A.

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Femoral-facial syndrome-prenatal diagnosis-autosomal dominant inheritance von Robinow, Meinhard, Sonek, Jiri, Buttino, Louis, Veghte, Anne

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Genée-wiedemann syndrome in a family von Robinow, Meinhard, Chen, Harold

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The Lenz-Majewski hyperostotic dwarfism. A syndrome of multiple congenital anomalies, mental retardation, and progressive skeletal sclerosis von Robinow, M, Johanson, A J, Smith, T H

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