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4. A case of chromosome abnormality (46, XX, Gq+) with congenital heart disease and leprechaunism. Iwaski H; Abe M; Nawate G; Kato H Jinrui Idengaku Zasshi; 1974 Jun; 19(1):82-3. PubMed ID: 4476865 [No Abstract] [Full Text] [Related]
5. [Partial deletion of the short arm of chromosome 4 (Wolf's syndrome). Two further cases]. Schinzel A; Schmid W Arch Genet (Zur); 1972; 45(2):88-98. PubMed ID: 4657590 [No Abstract] [Full Text] [Related]
6. [CNS pathology in hereditary syndromes of congenital developmental defects]. Ostrovskaia TI Arkh Patol; 1985; 47(10):42-8. PubMed ID: 3840990 [TBL] [Abstract][Full Text] [Related]
7. Syndromes and situations associated with congenital clavicular hypoplasia or agenesis. Hall BD Prog Clin Biol Res; 1982; 104():279-88. PubMed ID: 7163272 [No Abstract] [Full Text] [Related]
8. Ocular anomalies in malformation syndromes. Opitz JM Trans Am Acad Ophthalmol Otolaryngol; 1972; 76(5):1193-202. PubMed ID: 4199617 [No Abstract] [Full Text] [Related]
9. [Pathological anatomy of monogenic syndromes of multiple congenital developmental defects]. Cherstvoĭ ED; Laziuk GI; Lur'e IV; Ostrovskaia TI; Shved IA Arkh Patol; 1984; 46(4):39-45. PubMed ID: 6539587 [TBL] [Abstract][Full Text] [Related]
11. [Nijmegen's syndrome]. Kunz B; Teillac Hamel D; Girier B; Stephan JL; De Prost Y Ann Dermatol Venereol; 1992; 119(11):815-6. PubMed ID: 1301683 [No Abstract] [Full Text] [Related]
12. Dysmorphology report holoprosencephaly-polydactyly syndrome: affected brother and sister with a wide spectrum of anomalies. Delozier-Blanchet CD; Engel E Genet Couns; 1992; 3(1):57-8. PubMed ID: 1590983 [No Abstract] [Full Text] [Related]
13. Terminal deletion of the short arm of chromosome 3. Lizcano-Gil LA; Figuera LE Genet Couns; 1994; 5(1):35-8. PubMed ID: 8031533 [TBL] [Abstract][Full Text] [Related]