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22. Congenital emphysema, cryptorchidism, penoscrotal web, deafness, and mental retardation--a new syndrome? Lynch SA; Bushby KM Clin Dysmorphol; 1997 Jan; 6(1):35-7. PubMed ID: 9018416 [TBL] [Abstract][Full Text] [Related]
23. [Embryonic pathology caused by maternal phenylketonuria. A cause of underdiagnosed mental retardation. A report of 8 cases]. Campistol Plana J; Arellano Pedrola M; Poo Argüelles P; Escofet Sotera C; Pérez Olarte P; Vilaseca Buscà MA An Esp Pediatr; 1999 Aug; 51(2):139-42. PubMed ID: 10495499 [TBL] [Abstract][Full Text] [Related]
27. [Weaver syndrome. Apropos of a case]. Alvarez-Coca J; Fullana A; Morena V; Gonzalez M; Oliver A; Gracia R; Peralta A An Esp Pediatr; 1984 Oct; 21(6):626-8. PubMed ID: 6524773 [No Abstract] [Full Text] [Related]
28. [A study of the development of bone: II. Percentage estimation of bone age (author's transl)]. Li GZ Zhonghua Fang She Xue Za Zhi; 1979; 13(1):19-23. PubMed ID: 233080 [No Abstract] [Full Text] [Related]
29. Cornelia de Lange syndrome. Say B; Balci S; Atasu M Turk J Pediatr; 1969 Oct; 11(4):166-80. PubMed ID: 5402549 [No Abstract] [Full Text] [Related]
31. Studies of microcephalic primordial dwarfism I: approach to a delineation of the Seckel syndrome. Majewski F; Goecke T Am J Med Genet; 1982 May; 12(1):7-21. PubMed ID: 7046443 [No Abstract] [Full Text] [Related]
32. Cohen syndrome: further delineation and inheritance. Kousseff BG Am J Med Genet; 1981; 9(1):25-30. PubMed ID: 7246618 [TBL] [Abstract][Full Text] [Related]
33. MCA/MR syndrome with severe pre- and postnatal growth retardation, deep mental retardation, distinct facial appearance with nasal hypoplasia, cleft palate and retino-choroidal coloboma in two unrelated female patients. Fryns JP Genet Couns; 2000; 11(4):399-402. PubMed ID: 11140419 [TBL] [Abstract][Full Text] [Related]
34. The clinical course of mannosidosis. Autio S; Louhimo T; Helenius M Ann Clin Res; 1982 Apr; 14(2):93-7. PubMed ID: 7149616 [TBL] [Abstract][Full Text] [Related]
35. An exceptional Albanian family with seven children presenting with dysmorphic features and mental retardation: maternal phenylketonuria. Knerr I; Zschocke J; Schellmoser S; Topf HG; Weigel C; Dötsch J; Rascher W BMC Pediatr; 2005 Apr; 5(1):5. PubMed ID: 15811181 [TBL] [Abstract][Full Text] [Related]
37. [Epilepsy in childhood. Studies on material of a pediatric university clinic during a decade]. Stögmann W Wien Med Wochenschr; 1969 Dec; 119(49):845-9. PubMed ID: 4989194 [No Abstract] [Full Text] [Related]