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6 in total

1. Iminoglycinuria in a child in Czechoslovakia.

Authors: B Blehová; N Păzoutová; J Hyánek; J Jirásek
Journal: Humangenetik Date: 1973-07-20

Review 2. Diseases of Jews.

Authors: D M Krikler
Journal: Postgrad Med J Date: 1970-12 Impact factor: 2.401

3. Classic phenylketonuria: heterozygote detection during pregnancy.

Authors: R F Griffin; M E Humienny; E C Hall; L J Elsas
Journal: Am J Hum Genet Date: 1973-11 Impact factor: 11.025

4. Iminoglycinuria--a "harmless" inborn error of metabolism?

Authors: G R Fraser; A I Friedmann; V M Patton; D N Wade; L I Woolf
Journal: Humangenetik Date: 1968

5. Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters.

Authors: Stefan Bröer; Charles G Bailey; Sonja Kowalczuk; Cynthia Ng; Jessica M Vanslambrouck; Helen Rodgers; Christiane Auray-Blais; Juleen A Cavanaugh; Angelika Bröer; John E J Rasko
Journal: J Clin Invest Date: 2008-11-06 Impact factor: 14.808

6. Renal and intestinal hexose transport in familial glucose-galactose malabsorption.

Authors: L J Elsas; R E Hillman; J H Patterson; L E Rosenberg
Journal: J Clin Invest Date: 1970-03 Impact factor: 14.808

6 in total