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7 in total

1. New chromosomal dysmorphic syndromes. 2. Trisomy 10p.

Authors: S Stengel-Rutkowski; J D Murken; R Frankenberger; M Riechert; H Spiess; A Rodewald; J Stene
Journal: Eur J Pediatr Date: 1977-10-12 Impact factor: 3.183

2. A familial insertion involving an active nucleolar organiser within chromosome 12.

Authors: J L Watt; D A Couzin; D J Lloyd; G S Stephen; E McKay
Journal: J Med Genet Date: 1984-10 Impact factor: 6.318

3. Y autosome translocation and complex chromosome rearrangement in cri du chat syndrome.

Authors: J F Mattei; M G Mattei; J Coignet; F Giraud
Journal: J Med Genet Date: 1978-04 Impact factor: 6.318

4. Segregation of an insertional chromosome rearrangement in 3 generations.

Authors: K E Toomey; T Mohandas; R S Sparkes; M M Kaback; D L Rimoin
Journal: J Med Genet Date: 1978-10 Impact factor: 6.318

5. Partial trisomy 4 resulting from a complex maternal rearrangement of chromosomes 2, 4, and 18 with interstitial translocation.

Authors: M G Mattei; J F Mattei; R Bernard; F Giraud
Journal: Hum Genet Date: 1979-09-02 Impact factor: 4.132

Review 6. The Cri du Chat syndrome: epidemiology, cytogenetics, and clinical features.

Authors: E Niebuhr
Journal: Hum Genet Date: 1978-11-16 Impact factor: 4.132

7. Pure monosomy and trisomy 2q24.2----q3105 due to an inv ins(7;2)(q21.2;q3105q24.2) segregating in four generations.

Authors: M Moller; D García-Cruz; H Rivera; J Sánchez-Corona; J M Cantú
Journal: Hum Genet Date: 1984 Impact factor: 4.132

7 in total