MATERNAL SERUM ALPHA-FETOPROTEIN SCREENING IN 1987 von Simpson, Joe Leigh, Nadler, Henry L

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Antenatal detection of hereditary disorders von Nadler, H L

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Correction of γ-glutamyl transpeptidase deficiency in amniotic fluid of some cystic fibrosis fetuses by mixing with nondeficient fluids von BEN-YOSEPH, Y, REMBELSKI, P, NADLER, H. L

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MATERNAL SERUM AFP SCREENING: PROMISE NOT YET FULFILLED von Nadler, Henry L, Simpson, Joe Leigh

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The metabolism of sialic acid in cystic fibrosis von Ben-Yoseph, Y, Defranco, C L, Nadler, H L

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Congenital scalp defects with distal limb anomalies: Report of a family von Burton, Barbara K., Hauser, Lynn, Nadler, Henry L.

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Deficiency of arginine esterase in cystic fibrosis of the pancreas: demonstration of the proteolytic nature of the activity von Rao, G J, Nadler, H L

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Reaction of 4-methylumbelliferylguanidinobenzoate with proteases in human amniotic fluid von Walsh, M M, Rao, G J, Nadler, H L

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Clinical diagnosis of the inborn errors of metabolism in the neonatal period von Burton, Barbara K, Nadler, Henry L

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Schilder's disease: abnormal cholesterol retention and accumulation in cultivated fibroblasts von Burton, B K, Nadler, H L

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ANTENATAL DIAGNOSIS OF METABOLIC DISORDERS von BURTON, BARBARA K, NADLER, HENRY L

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Transport of L-cystine by cultivated skin fibroblasts of normal subjects and patients with cystinosis von Kaye, C I, Nadler, H L

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Reaction of 4-methylumbelliferylguanidinobenzoate with cultivated human skin fibroblasts derived from patients with cystic fibrosis von Platt, M W, Rao, G J, Nadler, H L

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Intrautrine Detection of Cystic Fibrosis von NADLER, HENRY L, WALSH, M M. J

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Tissue culture and antenatal detection of molecular diseases von Nadler, Henry L.

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Interallelic Complementation in Hybrid Cells Derived from Human Diploid Strains Deficient in Galactose-1-Phosphate Uridyl Transferase Activity von Nadler, Henry L., Chacko, Claramma M., Rachmeler, Martin

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Histidase Activity in Cultivated Human Amniotic Fluid Cells von Melancon, Serge B., Lee, Sally Y., Nadler, Henry L.

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Immunologic studies of arylsulfatase A in normal and metachromatic leukodystrophy liver von Shapira, E, DeGregorio, R R, Nadler, H L

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Absence of an α2-Macroglobulin-Protease Complex in Cystic Fibrosis von Shapira, Emmanuel, Rao, G J S, Wessel, Hans U, Nadler, Henry L

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Pompe's Disease: Detection of Heterozygotes by Lymphocyte Stimulation von Hirschhorn, Kurt, Nadler, Henry L., Waithe, William I., Brown, Barbara I., Hirschhorn, Rochelle

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