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3. Bowen-Conradi syndrome in an Indian infant: first non Hutterite case. Gupta A; Phadke SR Clin Dysmorphol; 2001 Apr; 10(2):155-6. PubMed ID: 11310999 [TBL] [Abstract][Full Text] [Related]
4. The Bowen-Conradi syndrome -- a highly lethal autosomal recessive syndrome of microcephaly, micrognathia, low birth weight, and joint deformities. Hunter AG; Woerner SJ; Montalvo-Hicks LD; Fowlow SB; Haslam RH; Metcalf PJ; Lowry RB Am J Med Genet; 1979; 3(3):269-79. PubMed ID: 484596 [TBL] [Abstract][Full Text] [Related]
5. A locus for Bowen-Conradi syndrome maps to chromosome region 12p13.3. Lamont RE; Loredo-Osti J; Roslin NM; Mauthe J; Coghlan G; Nylen E; Frappier D; Innes AM; Lemire EG; Lowry RB; Greenberg CR; Triggs-Raine BL; Morgan K; Wrogemann K; Fujiwara TM; Zelinski T Am J Med Genet A; 2005 Jan; 132A(2):136-43. PubMed ID: 15578624 [TBL] [Abstract][Full Text] [Related]
7. Microcephaly, micrognathia, and bird-headed dwarfism: prenatal diagnosis of a Seckel-like syndrome. Majoor-Krakauer DF; Wladimiroff JW; Stewart PA; van de Harten JJ; Niermeijer MF Am J Med Genet; 1987 May; 27(1):183-8. PubMed ID: 3300331 [TBL] [Abstract][Full Text] [Related]
8. Hypospadias as a new congenital anomaly in Bowen-Conradi syndrome. Aynaci FM; Mocan H; Erduran E; Gedik Y Genet Couns; 1994; 5(4):369-71. PubMed ID: 7888139 [No Abstract] [Full Text] [Related]
9. A Hutterite condition that mimics Bowen-Conradi syndrome. Flanagan JD; Reuter S; Crotwell PL; Myers A; De Berg K S D Med; 2015 Mar; 68(3):101-3. PubMed ID: 25906497 [TBL] [Abstract][Full Text] [Related]
10. Bowen-Conradi: a common Hutterite condition that mimics trisomy 18. Flanagan JD; Stein QP; Mroch AR; Deberg KL; Crotwell PL; Keppen LD S D Med; 2012 Jun; 65(6):221-3, 225. PubMed ID: 22856010 [TBL] [Abstract][Full Text] [Related]
17. Lambotte syndrome: microcephaly, holoprosencephaly, intrauterine growth retardation, facial anomalies, and early lethality--a new sublethal multiple congenital anomaly/mental retardation syndrome in four sibs. Verloes A; Dodinval P; Beco L; Bonnivert J; Lambotte C Am J Med Genet; 1990 Sep; 37(1):119-23. PubMed ID: 2240028 [TBL] [Abstract][Full Text] [Related]
18. [A newborn infant with the Bowen-Conradi syndrome; a fatal hereditary disorder]. Beemer FA; Gerards LJ Tijdschr Kindergeneeskd; 1982 Apr; 50(2):54-7. PubMed ID: 7123536 [No Abstract] [Full Text] [Related]
19. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome? Bindewald B; Ulmer H; Müller U Am J Med Genet; 1994 Apr; 50(2):173-6. PubMed ID: 8010348 [TBL] [Abstract][Full Text] [Related]
20. Neu-Laxova syndrome: report of a case from Turkey. Kuseyri F; Bilge I; Bilgiç L; Apak MY Clin Genet; 1993 May; 43(5):267-9. PubMed ID: 8375108 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]