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4. Structural abnormalities of chromosome 18. 3. Two G-18 translocations, one identified AS 22-18. Fraccaro M; Herin P; Hultén M; Ivemark BI; Jonasson J; Lindsten J; Tiepolo L; Zetterqvist P Ann Genet; 1972 Jun; 15(2):93-8. PubMed ID: 4537728 [No Abstract] [Full Text] [Related]
5. [Phenotype and karyotype interrelationships in chromosomal diseases]. Prokof'eva-Bel'govska ; Grinberg KN; Revazov AA; Mikel'saar AV; Kuliev AM Vestn Akad Med Nauk SSSR; 1973; 28(1):37-44. PubMed ID: 4797784 [No Abstract] [Full Text] [Related]
6. Frequency of chromosomal aberrations in newborn infants with multiple developmental defects. Chebotarev AN Sov Genet; 1974 Sep; 8(10):1329-30. PubMed ID: 4439048 [No Abstract] [Full Text] [Related]
7. [Comparative pathology of trisomies D and E]. Bocquet L Union Med Can; 1968 Jul; 97(7):907-23. PubMed ID: 5709533 [No Abstract] [Full Text] [Related]
8. [Clinical aspects of chromosomal aberrations - problems of semiotics and nosography]. Leiber B Padiatr Padol Suppl; 1975; 4():32-47. PubMed ID: 127146 [TBL] [Abstract][Full Text] [Related]
11. [Partial monosomy of chromosome 13. Study of 2 cases]. Carakushansky G; Büellerback AE AMB Rev Assoc Med Bras; 1979 Nov; 25(11):392-4. PubMed ID: 317731 [No Abstract] [Full Text] [Related]
12. [Complex cyanotic heart defect in a newborn infant with cat eye syndrome]. Paul T; Reimer A; Wilken M; Miller K; Kallfelz HC Monatsschr Kinderheilkd; 1991 Apr; 139(4):228-30. PubMed ID: 2072964 [TBL] [Abstract][Full Text] [Related]
13. [Morphodysplasias to chromosomal aberration]. Laurent C Rev Prat; 1974 Sep; 24(39):3445-59. PubMed ID: 4450088 [No Abstract] [Full Text] [Related]
14. 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]