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5. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome. Bonioli E; Palmieri A; Bertola A; Bellini C Genet Couns; 1995; 6(4):309-12. PubMed ID: 8775417 [TBL] [Abstract][Full Text] [Related]
6. [Medico-genetic study of the population of Turkmenistan. I. Hereditary diseases in 5 districts of the Ashkabad region]. Ginter EK; Revazov AA; Krasnopol'skaia KD; Akhimina NI; Iukina GP Genetika; 1980; 16(8):1487-94. PubMed ID: 6450714 [TBL] [Abstract][Full Text] [Related]
7. [Unusual form of obesity with an autosomal recessive type of heredity]. Akhmina NI; Ginter EK; Turaeva ShM Klin Med (Mosk); 1980 Jan; 58(1):63-6. PubMed ID: 6445019 [No Abstract] [Full Text] [Related]
8. Mammalian genetics: Determination of the radiation-induced mutation rate for sex-linked recessive lethals and visible autosomal genes in the mouse. ANL-7409. Grahn D; Craggs R; Leslie WP ANL Rep; 1967; ():110-1. PubMed ID: 5308199 [No Abstract] [Full Text] [Related]
9. Familial hydrocephalus of prenatal onset. Zlotogora J; Sagi M; Cohen T Am J Med Genet; 1994 Jan; 49(2):202-4. PubMed ID: 8116668 [TBL] [Abstract][Full Text] [Related]
10. [Regional characteristics of the incidence of hereditary pathology in Uzbekistan]. Gar'kavtseva RF; Ginter EK; Revazov AA Vestn Akad Med Nauk SSSR; 1984; (7):69-75. PubMed ID: 6236633 [No Abstract] [Full Text] [Related]
11. Consanguinity and genetic disorders. Profile from Jordan. Hamamy HA; Masri AT; Al-Hadidy AM; Ajlouni KM Saudi Med J; 2007 Jul; 28(7):1015-7. PubMed ID: 17603701 [TBL] [Abstract][Full Text] [Related]
12. Medical genetics and adoption. Schultz AL; Motulsky AG Child Welfare; 1971 Jan; 50(1):4-17. PubMed ID: 5170811 [No Abstract] [Full Text] [Related]
13. "Brittle" hair with short stature, intellectual impairment and decreased fertility: an autosomal recessive syndrome in an Amish kindred. Jackson CE; Weiss L; Watson JH Pediatrics; 1974 Aug; 54(2):201-7. PubMed ID: 4847854 [No Abstract] [Full Text] [Related]
15. Syndrome of osteoporosis with pseudoglioma. Bartsocas CS; Zeis PM; Elia M; Papadatos CJ Ann Genet; 1982; 25(1):61-2. PubMed ID: 6979303 [TBL] [Abstract][Full Text] [Related]
16. [Methods and indications for prenatal diagnosis. I. Elements of human genetics]. Masse A Union Med Can; 1983 Aug; 112(8):708-10, 712-3, 721. PubMed ID: 6636360 [No Abstract] [Full Text] [Related]
17. Congenital factor XIII deficiency. Shukla J; Dube B; Dube RK; Das BK; Mishra OP J Assoc Physicians India; 1993 Nov; 41(11):731. PubMed ID: 8005932 [No Abstract] [Full Text] [Related]
18. [A genetic study of pycnodysostosis]. de Almeida LM Ann Genet; 1972 Jun; 15(2):99-101. PubMed ID: 4537729 [No Abstract] [Full Text] [Related]