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11 in total

1. [Partial trisomy 11q and familial translocation 11--22 (author's transl)].

Authors: F Giraud; J F Mattei; M G Mattei; R Bernard
Journal: Humangenetik Date: 1975-08-25

2. The 11q-- syndrome: another case report.

Authors: M T Mulcahy; J Jenkyn
Journal: Hum Genet Date: 1977-04-15 Impact factor: 4.132

Review 3. Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases.

Authors: E K Pivnick; G V Velagaleti; R S Wilroy; M E Smith; S R Rose; R E Tipton; A T Tharapel
Journal: J Med Genet Date: 1996-09 Impact factor: 6.318

4. The 11q -- syndrome.

Authors: J Frank; V M Riccardi
Journal: Hum Genet Date: 1977-02-11 Impact factor: 4.132

5. Absence of constitutive heterochromatin in a partially identified supernumerary marker chromosome.

Authors: G S Pai; G H Thomas; P J Benke
Journal: J Med Genet Date: 1981-10 Impact factor: 6.318

6. Chromosomal investigations in children with pyknolepsy on dipropylacetate monotherapy.

Authors: F Kotlarek; J Faust
Journal: Hum Genet Date: 1978-09-19 Impact factor: 4.132

7. The 18 p-syndrome. Report of four cases.

Authors: J Faust; M Habedank; C Nieuwenhuijsen
Journal: Eur J Pediatr Date: 1976-08-16 Impact factor: 3.183

8. 11q aneuploidy: partial monosomy and trisomy in the children of a mother with a t(3;11)(p27;q23) translocation.

Authors: M A Ridler; J A McKeown
Journal: Hum Genet Date: 1979-11-01 Impact factor: 4.132

9. Partial deletion of long arm of chromosome 11[del(11)(q23)]: Jacobsen syndrome. Two new cases and review of the clinical findings.

Authors: A Schinzel; P Auf der Maur; H Moser
Journal: J Med Genet Date: 1977-12 Impact factor: 6.318

10. Craniosynostosis and syndactyly: expanding the 11q-- chromosomal deletion phenotype.

Authors: B M Lippe; R S Sparkes; B Fass; L Neidengard
Journal: J Med Genet Date: 1980-12 Impact factor: 6.318