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3. Pyloroduodenal atresia (diaphragm type): an autosomal recessive disease. Mishalany HG; Idriss ZH; Der Kaloustian VM Pediatrics; 1978 Sep; 62(3):419-21. PubMed ID: 704218 [No Abstract] [Full Text] [Related]
4. 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]
5. [Pedigree analysis of two families with Alport's syndrome]. Wässer S; Theile H; Schöne D; Lemme B Padiatr Grenzgeb; 1980; 19(3):167-71. PubMed ID: 7454376 [No Abstract] [Full Text] [Related]
6. [Current indications for chromosome study in congenital defects]. de la Chapelle A; Kääriäinen H; Salonen R Duodecim; 1981; 97(16):1320-32. PubMed ID: 7327123 [No Abstract] [Full Text] [Related]
7. [Partial trisomy C through a familial translocation t(Cq+;Cq-)]. Lejeune J; Rethoré MO; Berger R; Abonyi D; Dutrillaux B; See G Ann Genet; 1968 Sep; 11(3):171-5. PubMed ID: 5304617 [No Abstract] [Full Text] [Related]
8. Autosomal recessive congenital stenosis of aqueduct of Sylvius. Barros-Nuñes P; Rivas F Genet Couns; 1993; 4(1):19-23. PubMed ID: 8471217 [TBL] [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. [Glanzmann-Naegeli thrombasthenia. Study of a strongly endogamous ethnic group]. Lévy JM; Mayer G; Sacrez R; Ruff R; Francfort JJ; Rodier L Ann Pediatr (Paris); 1971 Feb; 18(2):129-37. PubMed ID: 5102406 [No Abstract] [Full Text] [Related]
11. 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]
12. Radial ray defects, renal ectopia, duodenal atresia and hydrocephalus: the extended spectrum for Fanconi anaemia. Evans DG; Rees HC; Spreadborough A; Campbell DJ; Gau GS; Pickering E; Hamilton S; Clayton-Smith J Clin Dysmorphol; 1994 Jul; 3(3):200-6. PubMed ID: 7981854 [TBL] [Abstract][Full Text] [Related]
14. [Familial occurrence of long arm deletion in chromosome 18 (46,18q-)]. Dziuba P; Jończyk K; Dziekanowska D; Bulsiewicz H Pediatr Pol; 1972 Aug; 47(8):1037-42. PubMed ID: 5074000 [No Abstract] [Full Text] [Related]
15. [Frequent familial occurrence of a multiplex malformation of the eye]. Nagy M; Fazekas A Klin Monbl Augenheilkd; 1971 Mar; 158(3):430-7. PubMed ID: 4995582 [No Abstract] [Full Text] [Related]
16. Letter: Familial microtia and meatal atresia. Dar H; Winter ST J Med Genet; 1973 Sep; 10(3):305-6. PubMed ID: 4774544 [No Abstract] [Full Text] [Related]
17. Syndactyly of the ring and small finger. De Smet L; Mulier T; Fabry G Genet Couns; 1994; 5(1):45-9. PubMed ID: 8031535 [TBL] [Abstract][Full Text] [Related]