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2. A SMALL AUTOSOMAL RING CHROMOSOME IN A FEMALE INFANT WITH CONGENITAL MALFORMATIONS. LUCAS M; KEMP NH; ELLIS JR; MARSHALL R Ann Hum Genet; 1963 Nov; 27():189-95. PubMed ID: 14081490 [No Abstract] [Full Text] [Related]
4. PROBABLE DELETION OF THE SHORT ARM OF CHROMOSOME 18. VANDYKE HE; VALDMANIS A; MANN JD Am J Hum Genet; 1964 Sep; 16(3):364-74. PubMed ID: 14207551 [No Abstract] [Full Text] [Related]
5. Familial deletion of the short arm of the D1-chromosome (46, XX, 13 p-) not associated with loss of haptoglobin or catalase activity. Parker CE; Koch R; Mavalwala J; Derencsenyi A; Hatashita A Clin Pediatr (Phila); 1969 Aug; 8(8):453-8. PubMed ID: 5797429 [No Abstract] [Full Text] [Related]
6. Chromosomal anomalies in cryptorchidism and hypospadias. Yamaguchi T; Kitada S; Osada Y Urol Int; 1991; 47(2):60-3. PubMed ID: 1686509 [TBL] [Abstract][Full Text] [Related]
7. A retarded child with a 46XX,3p-q+ chromosome karyotype. Butler LJ; Hall ME; Wharton BA J Ment Defic Res; 1974 Mar; 18(0):41-9. PubMed ID: 4424443 [No Abstract] [Full Text] [Related]
8. Mental retardation with facial abnormalities, broad thumbs and toes and unusual dermatoglyphics. Davison BC; Ellis HL; Kuzemko JA; Roberts DF Dev Med Child Neurol; 1967 Oct; 9(5):588-93. PubMed ID: 5587707 [No Abstract] [Full Text] [Related]
9. DELETION OF THE SHORT ARM OF CHROMOSOME 18. SUMMITT RL Cytogenetics; 1964; 3():201-6. PubMed ID: 14227324 [No Abstract] [Full Text] [Related]
10. Syndrome associated with a deficiency of part of the long arm of chromosome no. 18. Insley J Arch Dis Child; 1967 Apr; 42(222):140-6. PubMed ID: 4381584 [No Abstract] [Full Text] [Related]
11. ENLARGED CHROMOSOMAL SATELLITES ASSOCIATED WITH MENTAL RETARDATION AND DIGITAL ARCHES IN THREE GENERATIONS. JACOBSON TS; TISCHLER B; MILLER JR Ann Hum Genet; 1964 Sep; 28():21-6. PubMed ID: 14204849 [No Abstract] [Full Text] [Related]
12. Two cases with a C-group ring autosome. Atkins L; Pant SS; Hazard GW; Ouellette EM Ann Hum Genet; 1966 Jul; 30(1):1-6. PubMed ID: 5964028 [No Abstract] [Full Text] [Related]
13. [FAMILIAL SEGREGATION OF A 5-13 TRANSLOCATION DETERMINING PARTIAL MONOSOMY AND A TRISOMY OF THE SHORT ARM OF THE 5 CHROMOSOME: "CAT CRY" DISEASE AND ITS "RECEPROCAL"]. LEJEUNE J; LAFOURCADE J; BERGER R; TURPIN R C R Hebd Seances Acad Sci; 1964 Jun; 258():5767-70. PubMed ID: 14161436 [No Abstract] [Full Text] [Related]
14. A FAMILY WITH A FUSION TRANSLOCATION. WENAR C; RUTTENBERG BA; MELLMAN WJ; COOKE MS J Ment Defic Res; 1964 Dec; 8():SUPPL:93-101. PubMed ID: 14248583 [No Abstract] [Full Text] [Related]
15. CONGENITAL ASYMMETRY ASSOCIATED WITH DIPLOID-TRIPLOID MOSAICISM AND LARGE SATELLITES. FERRIER P; STALDER G; BAMATTER F; FERRIER S; BUEHLER E; KLEIN D Lancet; 1964 Jan; 1(7324):80-2. PubMed ID: 14075544 [No Abstract] [Full Text] [Related]
16. PARTIAL DELETION OF THE SHORT ARMS OF A CHROMOSOME OF THE 4-5 GROUP (DENVER). DYGGVE HV; MIKKELSEN M Arch Dis Child; 1965 Feb; 40(209):82-5. PubMed ID: 14259280 [No Abstract] [Full Text] [Related]
17. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study. Jacobsen P; Hauge M; Henningsen K; Hobolth N; Mikkelsen M; Philip J Hum Hered; 1973; 23(6):568-85. PubMed ID: 4134631 [No Abstract] [Full Text] [Related]
18. Twins, probably monozygotic: one mongoloid with 48 chromosomes, the other normal. Dekaban A Cytogenetics; 1965; 4(4):227-39. PubMed ID: 4222115 [No Abstract] [Full Text] [Related]