1,334 results on '"CHROMOSOME abnormalities"'
Search Results
2. NEONATOLOGY.
3. [FAMILIAL ANECEPHALY AND REARRANGEMENT OF 2 13-15 CHROMOSOMES].
4. PERSONAL OBSERVATIONS ON HYDATIDIFORM MOLE.
5. [STUDY TECHNICS FOR HUMAN CHROMOSOMES AND INDICATIONS OF THEIR USE].
6. [THE IMPORTANCE OF CHROMOSOME ANALYSIS FOR PRACTICAL CLINICAL DIAGNOSIS].
7. EMBRYONIC SEX DIFFERENTIATION, CONTROLLING FACTORS AND ABNORMALITIES, DIAGNOSIS AND TREATMENT.
8. [CHROMOSOMAL MOSAICISM: NORMAL-D-D, WITH MENTAL AND CORPOREAL DEVELOPMENTAL RETARDATION].
9. GROSS CHROMOSOMAL ABNORMALITY. CLINICAL AND LABORATORY AIDS IN THE DIAGNOSIS.
10. SOME AIDS IN THE DIAGNOSIS OF GENETIC DISORDERS.
11. A PATIENT WITH 48 CHROMOSOMES (XYYY).
12. [CONTRIBUTION TO THE DIAGNOSIS OF GONADAL DYSGENESIS].
13. MONGOLISM (DOWN'S SYNDROME) WITH ATYPICAL CLINICAL AND CYTOGENETIC FEATURES.
14. INDICATIONS FOR CHROMOSOME STUDIES.
15. GENITOGRAPHY IN INTERSEXUAL STATES.
16. [ADVANCES IN THE DIAGNOSIS OF HETEROZYGOUS FEATURES IN HEREDITARY METABOLIC DISEASES].
17. CEREBRO-METACARPO-METATARSAL DYSTROPHY (PSEUDO-PSEUDO HYPOPARATHYROIDISM) WITH CHROMOSOMAL ANOMALY.
18. KLINEFELTER'S SYNDROME WITH THE XXYY SEX CHROMOSOME COMPLEX. WITH PARTICULAR REFERENCE TO PREPUBERTAL DIAGNOSIS.
19. PRACTICAL POSSIBILITIES FOR CLASSIFICATION OF PRIMARY AMENORRHEA WITH SPECIAL REFERENCE TO THE USE OF PNEUMOPELVIGRAPHY.
20. [ORO-DIGITO-FACIAL SYNDROME IN 2 BROTHERS].
21. ABNORMALITIES OF THE SEX CHROMOSOME COMPLEMENT IN MAN.
22. THE VALUE OF CHROMOSOMAL STUDIES IN AN OUTPATIENT CLINIC: IN A HOSPITAL FOR SEVERELY RETARDED PATIENTS.
23. [CHROMOSOME ABNORMALITIES IN A PATIENT PRESENTING A HEMATODERMA MANIFESTED BY MONOCYTIC LEUKOSIS].
24. HUMAN CHROMOSOMES IN MEDICAL DIAGNOSIS.
25. BRACHMANN/DE LANGE SYNDROME.
26. A PHENOTYPIC FEMALE WITH 49 CHROMOSOMES, PRESUMABLY XXXXX. A CASE REPORT.
27. MENTAL RETARDATION: METHODS OF DIAGNOSIS AND SOME RECENTLY DESCRIBED SYNDROMES.
28. MICROTECHNIQUE FOR CULTURING LEUCOCYTES FOR IMPROVED SPREAD OF CHROMOSOMES.
29. NORMAL-TRISOMY 13-15 MOSAICISM IN TWO INFANTS.
30. Pre-natal counselling and diagnosis in Down's syndrome.
31. CLINICAL SIGNIFICANCE OF ANOMALIES OF THE SEX CHROMOSOMES.
32. [CHROMOSOMAL ANALYSIS IN MAN AS A CLINICAL METHOD].
33. THE SYNDROME OF PURE GONADAL DYSGENESIS.
34. INTERSEX.
35. CYTOGENETICS IN CLINICAL ENDOCRINOLOGY.
36. TWO XY SIBLINGS WITH GONADAL DYSGENESIS AND A FEMALE PHENOTYPE.
37. SOME PRACTICAL APPLICATIONS OF GENETICS IN MEDICINE AND SURGERY.
38. [CHROMOSOME INVESTIGATION IN HUMANS].
39. [PARTIAL DELETION OF THE LONG ARMS OF THE CHROMOSOME 18].
40. [HEREDITARY DISEASE].
41. FAMILIAL SUPRAVALVAR AORTIC STENOSIS.
42. A Diagnosis of Turner Syndrome in the Eighth Decade of Life.
43. Incidental Detection of a Chromosomal Aberration by Array-CGH in an Early Prenatal Diagnosis for Monogenic Disease on Coelomic Fluid.
44. Cytogenetic and Genetic Abnormalities with Diagnostic Value in Myelodysplastic Syndromes (MDS): Focus on the Pre-Messenger RNA Splicing Process.
45. Adrenocortical Tumors in Children With Constitutive Chromosome 11p15 Paternal Uniparental Disomy: Implications for Diagnosis and Treatment.
46. Case Report: Contiguous Xq22.3 Deletion Associated with ATS-ID Syndrome: From Genotype to Further Delineation of the Phenotype.
47. Hypodiploidy in a pediatric patient of T-cell acute lymphoblastic leukemia: a case report.
48. The Role of Cytogenetic Methods in the Diagnosis of Haematological Diseases.
49. Cytogenetic and Genetic Abnormalities with Diagnostic Value in Myelodysplastic Syndromes (MDS): Focus on the Pre-Messenger RNA Splicing Process
50. Investigating the Biomarkers of the Sasang Constitution via Network Pharmacology Approach.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.