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Literature DB >> 14296923

MUSCULAR DYSTROPHY (DUCHENNE) IN A GIRL WITH TURNER'S SYNDROME.

P FERRIER, F BAMATTER, D KLEIN.

Abstract

Entities: Species

Keywords: CHILD; GENETICS, HUMAN; KARYOMETRY; MUSCULAR DYSTROPHY; TURNER'S SYNDROME

Mesh：

Year: 1965 PMID： 14296923 PMCID： PMC1012803 DOI： 10.1136/jmg.2.1.38

Source DB: PubMed Journal: J Med Genet ISSN： 0022-2593 Impact factor: 6.318

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21 in total

1. INCIDENCE OF TURNER'S SYNDROME IN JAPANESE DWARFED GIRLS.

Authors: Y NAKAGOME; I HIBI; K KONOSHITA; T NAGAO; M AIKAWA
Journal: Lancet Date: 1963-08-24 Impact factor: 79.321

Review 2. GENETICS AND DISEASES OF MUSCLE.

Authors: S H BOYER; D C FAINER
Journal: Am J Med Date: 1963-11 Impact factor: 4.965

3. THE PATHOLOGY AND CYTOGENETICS OF GONADAL AGENESIS.

Authors: H W JONES; M A FERGUSON-SMITH; R H HELLER
Journal: Am J Obstet Gynecol Date: 1963-11-01 Impact factor: 8.661

4. THE XO SYNDROME. A STUDY OF THE DIFFERENTIATED PHENOTYPE IN 25 PATIENTS.

Authors: L LEMLI; D W SMITH
Journal: J Pediatr Date: 1963-10 Impact factor: 4.406

5. [GONADAL DYSGENESIS (TURNER'S SYNDROME): A RARE DISEASE BUT VALUABLE INSTRUCTIVELY; A CHROMOSOME STUDY OF 35 CASES].

Authors: E ENGEL
Journal: Schweiz Med Wochenschr Date: 1964-06-27

6. Abnormal sexual development associated with sex chromosome mosaicism. Report of three cases.

Authors: P FERRIER; S M GARTLER; S H WAXMAN; T H SHEPARD
Journal: Pediatrics Date: 1962-05 Impact factor: 7.124

7. Cytogenetic studies in primary amenorrhoea.

Authors: P A JACOBS; D G HARNDEN; K E BUCKTON; W M BROWN; M J KING; J A McBRIDE; T N MACGREGOR; N MACLEAN
Journal: Lancet Date: 1961-06-03 Impact factor: 79.321

8. Progressive muscular dystrophy of the Duchenne type in females and its mode of inheritance.

Authors: V DUBOWITZ
Journal: Brain Date: 1960-09 Impact factor: 13.501

9. Colour blindness and the Duchenne-type muscular dystrophy.

Authors: U PHILIP; C A SMITH; J N WALTON
Journal: Ann Hum Genet Date: 1956-11 Impact factor: 1.670

10. On the inheritance of muscular dystrophy; with a note on the blood groups, and a note on colour vision and linkage studies.

Authors: J N WALTON; R R RACE; U PHILIP
Journal: Ann Hum Genet Date: 1955-08 Impact factor: 1.670

16 in total

Review 1. [New data on the genetics and classification of muscular dystrophies].

Authors: P E Becker
Journal: Humangenetik Date: 1972

2. Genetic-epidemiological studies in progressive muscular dystrophy.

Authors: J Prot
Journal: J Med Genet Date: 1971-03 Impact factor: 6.318

3. [Biochemical, histological and clinical findings in a four-year-old female carrier of benign X-linked muscular dystrophy (Becker type)].

Authors: H Moser
Journal: Humangenetik Date: 1971

Review 4. Duchenne muscular dystrophy: pathogenetic aspects and genetic prevention.

Authors: H Moser
Journal: Hum Genet Date: 1984 Impact factor: 4.132

5. The female carrier of Duchenne muscular dystrophy.

Authors: V Dubowitz
Journal: Br Med J (Clin Res Ed) Date: 1982-05-15

6. Brother/sister pairs affected with early-onset, progressive muscular dystrophy: molecular studies reveal etiologic heterogeneity.

Authors: U Francke; B T Darras; J H Hersh; B O Berg; R G Miller
Journal: Am J Hum Genet Date: 1989-07 Impact factor: 11.025

7. Dual diagnoses in 152 patients with Turner syndrome: Knowledge of the second condition may lead to modification of treatment and/or surveillance.

Authors: Kelly L Jones; Erin A McNamara; Mauro Longoni; Danny E Miller; Mersedeh Rohanizadegan; Laura A Newman; Frances Hayes; Lynne L Levitsky; Betty L Herrington; Angela E Lin
Journal: Am J Med Genet A Date: 2018-08-06 Impact factor: 2.802