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7. Forearm fullness in Coffin-Lowry syndrome: a misleading yet possible early diagnostic clue. Hersh JH; Weisskopf B; DeCoster C Am J Med Genet; 1984 Jun; 18(2):195-9. PubMed ID: 6465196 [TBL] [Abstract][Full Text] [Related]
8. O--short stature with abnormalities of the cranium and limbs. Jorgenson RJ Birth Defects Orig Artic Ser; 1974; 10(5):249-51. PubMed ID: 4469995 [No Abstract] [Full Text] [Related]
9. [The "Charlie M." syndrome: a new clinical entity? Description of a case]. Bonioli E; Sbolgi P; Bernaola E; Pacciani G; Cottafava F Minerva Pediatr; 1980 May; 32(10):699-702. PubMed ID: 6779104 [No Abstract] [Full Text] [Related]
10. [Mucolipidosis Type II. STudy of 2 familial cases. Clinical and biochemical aspects]. Joannard A; Bost M; Pont J; Dieterlen M; Frappat P; Beaudoing A Pediatrie; 1974 Dec; 29(8):825-41. PubMed ID: 4218311 [No Abstract] [Full Text] [Related]
11. [Multiple malformation in a subject with D-D translocation]. Boncompagni P Minerva Pediatr; 1967 Nov; 19(47):2107-13. PubMed ID: 5606106 [No Abstract] [Full Text] [Related]
13. ["V.A.C.T.E.R.L.": a new complex of congenital multiple abnormalities as a possible consequence of the teratogenic action of exogenous hormones taken during pregnancy]. Buffoni L; Tarateta A; Pecorari D Minerva Ginecol; 1976 May; 28(5):382-91. PubMed ID: 1018820 [No Abstract] [Full Text] [Related]
14. A suspected case of Abruzzo-Erickson syndrome. Kidner G; Taylor J; Patton MA; Taylor N Cleft Palate Craniofac J; 2004 Sep; 41(5):565-7. PubMed ID: 15352866 [TBL] [Abstract][Full Text] [Related]
15. Epidemiology of limb-body wall complex in Japan. Kurosawa K; Imaizumi K; Masuno M; Kuroki Y Am J Med Genet; 1994 Jun; 51(2):143-6. PubMed ID: 8092190 [TBL] [Abstract][Full Text] [Related]
16. New syndrome of macrocephaly, hypertelorism, short limbs, hearing loss, and developmental delay. Bagatelle R; Cassidy SB Am J Med Genet; 1995 Jan; 55(3):367-71. PubMed ID: 7537019 [TBL] [Abstract][Full Text] [Related]
17. Congenital malformations of the hand and forearm in children: what radiologists should know. Aucourt J; Budzik JF; Manouvrier-Hanu S; Mézel A; Cotten A; Boutry N Semin Musculoskelet Radiol; 2012 Apr; 16(2):146-58. PubMed ID: 22648430 [TBL] [Abstract][Full Text] [Related]
18. Craniofacial, limb, and abdominal anomalies in a distinct syndrome: relation to the spectrum of Pfeiffer syndrome type 3. Barone CM; Marion R; Shanske A; Argamaso RV; Shprintzen RJ Am J Med Genet; 1993 Mar; 45(6):745-50. PubMed ID: 8456855 [TBL] [Abstract][Full Text] [Related]
19. [Ultrasonographic diagnosis of a combined malformation syndrome - hydrocephalus - evisceration and dysplasia of the extremities (author's transl)]. Schmidt W; Heberling D; Boos R; Heinrich D Z Geburtshilfe Perinatol; 1981 Jun; 185(3):183-6. PubMed ID: 7196655 [TBL] [Abstract][Full Text] [Related]
20. [Skeletal changes in a case of unusual chromosome aberration. (Patient with chromosome complex 48, XXXX-49, XXXXX: comparison with the syndrome 49,XXXXY]. Dallapiccola B; Pistocchi GF Radiol Med; 1968 Aug; 54(8):737-50. PubMed ID: 5190487 [No Abstract] [Full Text] [Related] [Next] [New Search]