These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
42. Limb reduction defects and renal dysplasia: confirmation of a new, apparently lethal, autosomal recessive MCA syndrome. Schrander-Stumpel C; de Die-Smulders C; Fryns JP; da Costa J; Bouckaert P Am J Med Genet; 1990 Sep; 37(1):133-5. PubMed ID: 2240030 [TBL] [Abstract][Full Text] [Related]
43. [Congenital functional disorders of the hypothalamus caused by a development disorder of the prosencephalon]. Ceelie N; Steendijk R Tijdschr Kindergeneeskd; 1981 Apr; 49(2):66-73. PubMed ID: 7268757 [TBL] [Abstract][Full Text] [Related]
44. RAPADILINO syndrome with radial and patellar aplasia/hypoplasia as main manifestations. Kääriäinen H; Ryöppy S; Norio R Am J Med Genet; 1989 Jul; 33(3):346-51. PubMed ID: 2801769 [TBL] [Abstract][Full Text] [Related]
45. A new short rib syndrome: report of two cases. Beemer FA; Langer LO; Klep-de Pater JM; Hemmes AM; Bylsma JB; Pauli RM; Myers TL; Haws CC Am J Med Genet; 1983 Jan; 14(1):115-23. PubMed ID: 6829599 [TBL] [Abstract][Full Text] [Related]
46. The genetics of hand malformations. Temtamy SA; McKusick VA Birth Defects Orig Artic Ser; 1978; 14(3):i-xviii, 1-619. PubMed ID: 215242 [No Abstract] [Full Text] [Related]
47. Mental retardation with pterygia, shortness and distinct facial appearance. A new MCA/MR syndrome. Haspeslagh M; Fryns JP; de Mûelenaere A; Schautteet L; van Eeckhoutte I; van den Berghe H Clin Genet; 1985 Dec; 28(6):550-5. PubMed ID: 4075567 [TBL] [Abstract][Full Text] [Related]
48. Case of lethal multiple pterygium syndrome with special reference to the origin of pterygia. Hartwig NG; Vermeij-Keers C; Bruijn JA; van Groningen K; Ottervanger HP; Holm JP Am J Med Genet; 1989 Aug; 33(4):537-41. PubMed ID: 2531978 [TBL] [Abstract][Full Text] [Related]
49. Familial transmission of a dysmorphic syndrome: a variant example of Kabuki syndrome? Belengeanu V; Rozsnyai K; Farcaş S; Velea I; Fryns JP Genet Couns; 2005; 16(2):167-71. PubMed ID: 16080297 [TBL] [Abstract][Full Text] [Related]
50. Filippi syndrome: report of three additional cases. Williams MS; Williams JL; Wargowski DS; Pauli RM; Pletcher BA Am J Med Genet; 1999 Nov; 87(2):128-33. PubMed ID: 10533026 [TBL] [Abstract][Full Text] [Related]