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4. The enzymatic expression of heterozygosity in families of children with galactosemia. DONNELL GN; BERGREN WR; BRETTHAUER RK; HANSEN RG Pediatrics; 1960 Apr; 25():572-81. PubMed ID: 13817542 [No Abstract] [Full Text] [Related]
5. What does it mean to be a carrier for a metabolic disease? Kaye EM Ann Neurol; 2002 Nov; 52(5):530-1. PubMed ID: 12402247 [No Abstract] [Full Text] [Related]
6. [Hereditary metabolic diseases and their recognition]. JONXIS JH Ned Tijdschr Geneeskd; 1960 Jan; 104():271-2. PubMed ID: 14407846 [No Abstract] [Full Text] [Related]
16. [Clinical demonstrations of hereditary disorders of metabolism]. Marti HR Schweiz Med Wochenschr; 1980 Dec; 110(49):1857-63. PubMed ID: 7455656 [TBL] [Abstract][Full Text] [Related]
17. The metabolic basis of some inborn intellectual disorders in adolescents. KUGELMASS IN Int Rec Med; 1961 Mar; 174():156-79. PubMed ID: 13754939 [No Abstract] [Full Text] [Related]
18. [THE FREQUENCY IN JAPAN OF CARRIERS OF THE RARE 'RECESSIVE' GENE CAUSING ACATALASEMIA]. HAMILTON HB; NEEL JV; KOBARA TY Jinrui Idengaku Zasshi; 1963 Sep; 8():163-76. PubMed ID: 14115911 [No Abstract] [Full Text] [Related]