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10 in total

1. Prenatal diagnosis of 45,X/46,XY mosaicism with postnatal confirmation in a phenotypically normal male infant.

Authors: L Y Hsu; H J Kim; R Hausknecht; K Hirschhorn
Journal: Clin Genet Date: 1976-10 Impact factor: 4.438

2. Non-fluorescent and non-heterochromatic Y chromosome in 45, X 46,XY mosaicism.

Authors: L Y Hsu; H J Kim; S Paciuc; L Steinfeld; K HirshhorHirschhorn
Journal: Ann Genet Date: 1974-03

3. Three cases of sex chromosome mosaicism with a nonfluorescent Y.

Authors: K Madan; L Gooren; J Schoemaker
Journal: Hum Genet Date: 1979-02-15 Impact factor: 4.132

4. A theory explaining the abnormality in 45,X/46,XY mosaicism with non-fluorescent Y chromosome. presentation of three cases.

Authors: B Kaluzewski; A Jokinen; H Hortling; A de la Chapelle
Journal: Ann Genet Date: 1978-03

5. Two dicentric Y isochromosomes, one without and the Yqh heterochromatic segment: review of the Y isochromosomes.

Authors: A Daniel; N Lyons; J H Casey; L Gras
Journal: Hum Genet Date: 1980 Impact factor: 4.132

6. Non-fluorescent Y-chromosome in mixed gonadal dysgenesis with 45,X/46,XY mosaicism.

Authors: J P Fryns; J C Pedersen; P Goddeeris; H van den Berghe
Journal: Ann Genet Date: 1980

7. Modification of DAPI banding on human chromosomes by prestaining with a DNA-binding oligopeptide antibiotic, distamycin A.

Authors: D Schweizer; P Ambros; M Andrle
Journal: Exp Cell Res Date: 1978-02 Impact factor: 3.905

8. Translocations causing non-fluorescent Y chromosomes in human XO/XY mosaics.

Authors: T Caspersson; M Hultén; J Jonasson; J Lindsten; A Therkelsen; L Zech
Journal: Hereditas Date: 1971 Impact factor: 3.271

9. Non-fluorescent Y chromosome in a male infant with Turner's symptoms and XO/XY mosaicism.

Authors: C Fonatschi; S D Flatz; R Freymann
Journal: Clin Genet Date: 1977-03 Impact factor: 4.438

10. Gonadal dysgenesis with mosaicism and a nonfluorescent Y chromosome: report of two cases with correlation of clinical, pathologic, and cytogenetic findings.

Authors: W R Curtis; B J White; A W Lucky; N Roche-Bender; D R Knab; R E Johnsonbaugh
Journal: Am J Obstet Gynecol Date: 1980-03-01 Impact factor: 8.661

10 in total

6 in total

1. Identification and characterization of normal length nonfluorescent Y chromosomes: cytogenetic analysis, southern hybridization and non-isotopic in situ hybridization.

Authors: F Speleman; B Van der Auwera; K Mangelschots; M Vercruyssen; T Raap; J Wiegant; M Craen; J Leroy
Journal: Hum Genet Date: 1990-10 Impact factor: 4.132

Distamycin A-DAPI banding of nonfluorescent Y(Ynf) chromosomes in 45,X/46,XYnf mosaicism.

1. Prenatal diagnosis of 45,X/46,XY mosaicism with postnatal confirmation in a phenotypically normal male infant.

2. Non-fluorescent and non-heterochromatic Y chromosome in 45, X 46,XY mosaicism.

3. Three cases of sex chromosome mosaicism with a nonfluorescent Y.

4. A theory explaining the abnormality in 45,X/46,XY mosaicism with non-fluorescent Y chromosome. presentation of three cases.

5. Two dicentric Y isochromosomes, one without and the Yqh heterochromatic segment: review of the Y isochromosomes.

6. Non-fluorescent Y-chromosome in mixed gonadal dysgenesis with 45,X/46,XY mosaicism.

7. Modification of DAPI banding on human chromosomes by prestaining with a DNA-binding oligopeptide antibiotic, distamycin A.

8. Translocations causing non-fluorescent Y chromosomes in human XO/XY mosaics.

9. Non-fluorescent Y chromosome in a male infant with Turner's symptoms and XO/XY mosaicism.

10. Gonadal dysgenesis with mosaicism and a nonfluorescent Y chromosome: report of two cases with correlation of clinical, pathologic, and cytogenetic findings.

1. Identification and characterization of normal length nonfluorescent Y chromosomes: cytogenetic analysis, southern hybridization and non-isotopic in situ hybridization.

2. Characterisation of a satellited non-fluorescent Y chromosome (Y[nfqs]) by FISH.

3. Short arm dicentric Y chromosome with associated statural defects in a sterile man.

4. Hae III restriction of DNA from three cases with nonfluorescent Y chromosomes (45XO/46XYnf).

5. Three cases of 45,X/46,XYnf mosaicism. Molecular analysis revealed heterogeneity of the nonfluorescent Y chromosome.

6. Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypes.