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Literature DB >> 13690987

A probable XXYY sex determining mechanism in a mentally defective male with Klinefelter's syndrome.

D H CARR, M L BARR, E R PLUNKETT.

Abstract

Entities: Disease

Keywords: MENTAL DEFICIENCY/case reports; SEX DETERMINATION

Mesh：

Year: 1961 PMID： 13690987 PMCID： PMC1939500

Source DB: PubMed Journal: Can Med Assoc J ISSN： 0008-4409 Impact factor: 8.262

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23 in total

1. Sex chromatin, sex chromosomes and sex anomalies.

Authors: M L BARR; D H CARR
Journal: Can Med Assoc J Date: 1960-11-05 Impact factor: 8.262

2. A presumptive human XXY/XX mosaic.

Authors: C E FORD; P E POLANI; J H BRIGGS; P M BISHOP
Journal: Nature Date: 1959-04-11 Impact factor: 49.962

3. An XXXX sex chromosome complex in two mentally defective females.

Authors: D H CARR; M L BARR; E R PLUNKETT
Journal: Can Med Assoc J Date: 1961-01-21 Impact factor: 8.262

4. Chromosomal trisomy associated with the Sturge-Weber syndrome.

Authors: M D HAYWARD; B D BOWER
Journal: Lancet Date: 1960-10-15 Impact factor: 79.321

5. Primary amentia and micro-orchidism associated with an XXXY sex-chromosome constitution.

Authors: M A FERGUSON-SMITH; A W JOHNSTON; S D HANDMAKER
Journal: Lancet Date: 1960-07-23 Impact factor: 79.321

6. The chromosomes in two patients with Klinefelter syndrome.

Authors: S BERGMAN; J REITALU; H NOWAKOWSKI; W LENZ
Journal: Ann Hum Genet Date: 1960-04 Impact factor: 1.670

7. Chromosomal translocations in mongolism and in normal relatives.

Authors: L S PENROSE; J R ELLIS; J D DELHANTY
Journal: Lancet Date: 1960-08-20 Impact factor: 79.321

8. [The etiology of Klinefelter's syndrome: a contribution to chromosome pathology in the human].

Authors: W LENZ; H NOWAKOWSKI; A PRADER; C SCHIRREN
Journal: Schweiz Med Wochenschr Date: 1959-07-11

9. [Chromosome aberrations and human diseases. XXY Klinefelter's syndrome from 46 chromosomes caused by T-T centromeric fusion].

Authors: J LEJEUNE; R TURPIN; J DECOURT
Journal: C R Hebd Seances Acad Sci Date: 1960-03-28

10. Chromation-positive Klinefelter's syndrome (primary microrchidism) in a mental-deficiency hospital.

Authors: M A FERGUSON-SMITH
Journal: Lancet Date: 1958-05-03 Impact factor: 79.321

15 in total

1. DERMATOGLYPHICS ASSOCIATED WITH THE XXYH CHROMOSOME COMPLEMENT.

Authors: I A UCHIDA; J R MILLER; H C SOLTAN
Journal: Am J Hum Genet Date: 1964-09 Impact factor: 11.025

Review 2. [ON THE CLINICAL ASPECTS AND HISTOPATHOLOGY OF PRIMARY MALE HYPOGONADISM. 2. CASTRATISM AND SO-CALLED KLINEFELTER'S SYNDROME AS DISEASE FORMS WITH KNOWN ETIOLOGY].

Authors: O HORNSTEIN
Journal: Arch Klin Exp Dermatol Date: 1963-09-02

Review 3. [ON THE CLINICAL ASPECTS AND HISTOPATHOLOGY OF PRIMARY MALE HYPOGONADISM. 1. NOSOLOGICAL CLASSIFICATION OF MALE HYPOGONADISM].

Authors: O HORNSTEIN
Journal: Arch Klin Exp Dermatol Date: 1963-09-02

A probable XXYY sex determining mechanism in a mentally defective male with Klinefelter's syndrome.

1. Sex chromatin, sex chromosomes and sex anomalies.

2. A presumptive human XXY/XX mosaic.

3. An XXXX sex chromosome complex in two mentally defective females.

4. Chromosomal trisomy associated with the Sturge-Weber syndrome.

5. Primary amentia and micro-orchidism associated with an XXXY sex-chromosome constitution.

6. The chromosomes in two patients with Klinefelter syndrome.

7. Chromosomal translocations in mongolism and in normal relatives.

8. [The etiology of Klinefelter's syndrome: a contribution to chromosome pathology in the human].

9. [Chromosome aberrations and human diseases. XXY Klinefelter's syndrome from 46 chromosomes caused by T-T centromeric fusion].

10. Chromation-positive Klinefelter's syndrome (primary microrchidism) in a mental-deficiency hospital.

1. DERMATOGLYPHICS ASSOCIATED WITH THE XXYH CHROMOSOME COMPLEMENT.

Review 2. [ON THE CLINICAL ASPECTS AND HISTOPATHOLOGY OF PRIMARY MALE HYPOGONADISM. 2. CASTRATISM AND SO-CALLED KLINEFELTER'S SYNDROME AS DISEASE FORMS WITH KNOWN ETIOLOGY].

Review 3. [ON THE CLINICAL ASPECTS AND HISTOPATHOLOGY OF PRIMARY MALE HYPOGONADISM. 1. NOSOLOGICAL CLASSIFICATION OF MALE HYPOGONADISM].

4. KLINEFELTER'S SYNDROME DUE TO XXYY CHROMOSOME ANOMALY.

5. Dizygotic twin with XXYY chromosome aneuploidy and diffuse sexual orientation, with review of 30 XXYY cases.

6. Sex chromosome aberrations in schizophrenia.

7. A family with a large Y chromosome.

8. The influence of inactive chromosomes on human development. Anomalous sex chromosome complements and the phenotype.

9. Sex chromatin survey in mentally handicapped children in Mexico.

10. A survey of sex chromatin abnormalities in mental hospitals.