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2. Hypoplastic left heart. Evidence for possible autosomal recessive inheritance. Shokeir MH Birth Defects Orig Artic Ser; 1974; 10(4):223-7. PubMed ID: 4470892 [TBL] [Abstract][Full Text] [Related]
3. Familial hypoplastic left heart syndrome. Van Egmond H; Defloor E; Kunnen M; Carton D Acta Paediatr Belg; 1976; 29(1):25-8. PubMed ID: 1015290 [No Abstract] [Full Text] [Related]
4. Arteriohepatic dysplasia: familial pulmonary arterial stenosis with neonatal liver disease. Watson GH; Miller V Arch Dis Child; 1973 Jun; 48(6):459-66. PubMed ID: 4712776 [TBL] [Abstract][Full Text] [Related]
5. Genetics of conotruncal malformations: further evidence of autosomal recessive inheritance. Rein AJ; Sheffer R Am J Med Genet; 1994 Apr; 50(3):302-3. PubMed ID: 8042678 [No Abstract] [Full Text] [Related]
6. Probable autosomal recessive inheritance of polysplenia, situs inversus and cardiac defects in an Amish family. Arnold GL; Bixler D; Girod D Am J Med Genet; 1983 Sep; 16(1):35-42. PubMed ID: 6638068 [TBL] [Abstract][Full Text] [Related]
7. [Epidemiological and genetic study of 3 congenital cardiopathies with neonatal disclosure]. Briard ML; Chauvet ML; Le Merrer M; Frezal J Arch Fr Pediatr; 1984 May; 41(5):313-21. PubMed ID: 6466030 [TBL] [Abstract][Full Text] [Related]
8. Melnick-Needles syndrome: indication for an autosomal recessive form. ter Haar B; Hamel B; Hendriks J; de Jager J Am J Med Genet; 1982 Dec; 13(4):469-77. PubMed ID: 7158646 [TBL] [Abstract][Full Text] [Related]
9. Congenital chloride diarrhea, an autosomal recessive disease. Genetic study of 14 Finnish and 12 other families. Norio R; Perheentupa J; Launiala K; Hallman N Clin Genet; 1971; 2(3):182-92. PubMed ID: 5111762 [No Abstract] [Full Text] [Related]
10. Familial holoprosencephaly, heart defects, and polydactyly. Hennekam RC; van Noort G; de la Fuente AA Am J Med Genet; 1991 Nov; 41(2):258-62. PubMed ID: 1785646 [TBL] [Abstract][Full Text] [Related]