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3. FAMILIAL MOSAICISM OF A CHROMOSOME 16 ABNORMALITY ASSOCIATED WITH MULTIPLE CONGENITAL ANOMALIES. TIPS RL; SMITH GS; MEYER DL; PERKINS AL Am J Ment Defic; 1964 Nov; 69():330-40. PubMed ID: 14223550 [No Abstract] [Full Text] [Related]
4. [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]
5. A CASE OF DOUBLE AUTOSOMAL TRISOMY WITH MOSAICISM: 48/XX (TRISOMY 18+21) AND 46/XX. HSU LY; SCHWANGER AJ; NEMHAUSER I; SOBEL EH J Pediatr; 1965 Jun; 66():1055-60. PubMed ID: 14288459 [No Abstract] [Full Text] [Related]
9. [CHROMOSOME ABNORMALITIES AND HUMAN DISEASES. CONTRIBUTION TO THE ANATOMICAL STUDY OF TRISOMY 13]. LAFOURCADE J; BOCQUET L; CRUVEILLER J; SARAUX H; BERGER R; LEJEUNE J; HUETDEBAROCHEZ Y; TURPIN R Bull Mem Soc Med Hop Paris; 1964 Mar 6-13; 115():383-99. PubMed ID: 14156094 [No Abstract] [Full Text] [Related]
10. Partial monosomy 8p and partial trisomy 8p with moderate mental retardation. van Balkom ID; Hagendoorn J; De Pater JM; Hennekam RC Genet Couns; 1992; 3(2):83-9. PubMed ID: 1642815 [TBL] [Abstract][Full Text] [Related]
12. [FAMILIAL OCCURRENCE OF AN ABNORMAL D-CHROMOSOME]. WOLF U; BAITSCH H; KUENZER W; REINWEIN H Cytogenetics; 1964; 3():112-23. PubMed ID: 14190610 [No Abstract] [Full Text] [Related]
13. The significance of dermatoglyphics in medicine. A short survey and summary. Holt SB Clin Pediatr (Phila); 1973 Aug; 12(8):471-84. PubMed ID: 4579966 [No Abstract] [Full Text] [Related]
14. A pedigree of 4/18 translocation chromosomes with type and countertype partial trisomy and partal monosomy for chromosome 18. Valdmanis A; Pearson G; Siegel AE; Hoeksema RH; Mann JD Ann Genet; 1967 Dec; 10(4):159-66. PubMed ID: 5301688 [No Abstract] [Full Text] [Related]
16. TRISOMY-18 SYNDROME IN A PATIENT WITH NORMAL KARYOTYPE, CLINICAL AND DERMATOGLYPHIC FINDINGS. HOOK EB; YUNIS JJ JAMA; 1965 Sep; 193():840-3. PubMed ID: 14329998 [No Abstract] [Full Text] [Related]
17. [MONGOL CHILD-MOSAIC PARENT. STUDY OF 2 FAMILIES]. FERRIER S J Genet Hum; 1964 Dec; 13():315-36. PubMed ID: 14269571 [No Abstract] [Full Text] [Related]
18. [Clinical anatomic and histopathological study of ocular signs in 2 cases of mosaicism associated with autosomal 18-21 double trisomy]. Laliam M; Laliam N; Ouadahi MS; Iles S; Ould Larbi L Bull Mem Soc Fr Ophtalmol; 1972; 85(0):83-90. PubMed ID: 4211332 [No Abstract] [Full Text] [Related]
19. PARTIAL TRISOMY-DEFICIENCY SYNDROME RESULTING FROM A RECIPROCAL TRANSLOCATION IN A LARGE KINDRED. UCHIDA IA; WANG HC; LAXDAL OE; ZALESKI WA; DUNCAN BP Cytogenetics; 1964; 3():81-96. PubMed ID: 14190616 [No Abstract] [Full Text] [Related]
20. 46,XY-47,XY,C+ mosaicism in a male infant with multiple anomalies. Oikawa K; Kajii T; Shimba H; Sasaki M Ann Genet; 1969 Jun; 12(2):102-6. PubMed ID: 5308379 [No Abstract] [Full Text] [Related] [Next] [New Search]