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A case of monosomy G?

作者信息

Hall B, Fredga K, Svenningsen N

出版信息

Hereditas. 1967;57(3):356-64. doi: 10.1111/j.1601-5223.1967.tb02118.x.

DOI:10.1111/j.1601-5223.1967.tb02118.x

PMID:5587100

Abstract

摘要

相似文献

A case of monosomy G?

Hereditas. 1967;57(3):356-64. doi: 10.1111/j.1601-5223.1967.tb02118.x.

Monosomy for a G autosome.

Arch Dis Child. 1969 Feb;44(233):113-9. doi: 10.1136/adc.44.233.113.

[A case with mosaicism of partial monosomy G- monosomy G in peripheral blood lymphocytes].

Humangenetik. 1968;6(4):303-10.

21-Monosomy in a liveborn male infant.

Eur J Pediatr. 1983 Mar;140(1):57-9. doi: 10.1007/BF00661907.

[Viability in monosomy G].

Monatsschr Kinderheilkd (1902). 1969 Apr;117(4):184-7.

[Partial monosomy of a chromosome of the group G (21 q-) associated with mesomelic nanism with dominat autosomal transmission].

Minerva Pediatr. 1977 Jun 16;29(21):1341-8.

De novo partial monosomy 21 with unusual karyotype.

Jinrui Idengaku Zasshi. 1986 Mar;31(1):45-8. doi: 10.1007/BF01876801.

[Monosomy of chromosome 21].

Pediatr Pol. 1983 Jun;58(6):557-9.

[Monosomy 21, G-deletion syndrome I, Anti-mongolism].

Ugeskr Laeger. 1974 Aug 12;136(33):1857.

Partial monosomy of a G group chromosome (45,XY,G-46,XY,Gr): report of a new case.

Ann Genet. 1971 Mar;14(1):7-12.

引用本文的文献

"Antimongolism" syndrome.

Br Med J. 1969 Oct 18;4(5676):148-9. doi: 10.1136/bmj.4.5676.148.

[A case with mosaicism of partial monosomy G- monosomy G in peripheral blood lymphocytes].

Humangenetik. 1968;6(4):303-10.

Monosomy G: case report and review of the literature.

J Med Genet. 1971 Dec;8(4):496-500. doi: 10.1136/jmg.8.4.496.

Group G deletion syndromes.

J Med Genet. 1971 Sep;8(3):341-5. doi: 10.1136/jmg.8.3.341.

A child with a ring G chromosome (46,XX, Gr).

J Med Genet. 1971 Jun;8(2):231-4. doi: 10.1136/jmg.8.2.231.

A 45,XX,21--child: attempt at a cytological and clinical interpretation of the karyotype.

J Med Genet. 1972 Mar;9(1):110-5. doi: 10.1136/jmg.9.1.110.

Mental retardation, unusual facies, and abnormal nails associated with a group-G ring chromosome. A case report on two unrelated cases.

J Med Genet. 1971 Jun;8(2):195-201. doi: 10.1136/jmg.8.2.195.

[Ring G-chromosome. Report of two cases and review of literature].

Humangenetik. 1971;12(2):142-55. doi: 10.1007/BF00291470.

Karyotype 45,XX,-21/46,XX,21q-in an infant with symptoms of G-deletion syndrome I.

J Med Genet. 1974 Dec;11(4):389-93. doi: 10.1136/jmg.11.4.389.

A male infant with monosomy 21.

Humangenetik. 1975 Aug 29;29(1):1-7. doi: 10.1007/BF00273344.

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相似文献

A case of monosomy G?

Hereditas. 1967;57(3):356-64. doi: 10.1111/j.1601-5223.1967.tb02118.x.

Monosomy for a G autosome.

Arch Dis Child. 1969 Feb;44(233):113-9. doi: 10.1136/adc.44.233.113.

[A case with mosaicism of partial monosomy G- monosomy G in peripheral blood lymphocytes].

Humangenetik. 1968;6(4):303-10.

21-Monosomy in a liveborn male infant.

Eur J Pediatr. 1983 Mar;140(1):57-9. doi: 10.1007/BF00661907.

[Viability in monosomy G].

Monatsschr Kinderheilkd (1902). 1969 Apr;117(4):184-7.

[Partial monosomy of a chromosome of the group G (21 q-) associated with mesomelic nanism with dominat autosomal transmission].

Minerva Pediatr. 1977 Jun 16;29(21):1341-8.

De novo partial monosomy 21 with unusual karyotype.

Jinrui Idengaku Zasshi. 1986 Mar;31(1):45-8. doi: 10.1007/BF01876801.

[Monosomy of chromosome 21].

Pediatr Pol. 1983 Jun;58(6):557-9.

[Monosomy 21, G-deletion syndrome I, Anti-mongolism].

Ugeskr Laeger. 1974 Aug 12;136(33):1857.

Partial monosomy of a G group chromosome (45,XY,G-46,XY,Gr): report of a new case.

Ann Genet. 1971 Mar;14(1):7-12.

引用本文的文献

"Antimongolism" syndrome.

Br Med J. 1969 Oct 18;4(5676):148-9. doi: 10.1136/bmj.4.5676.148.

[A case with mosaicism of partial monosomy G- monosomy G in peripheral blood lymphocytes].

Humangenetik. 1968;6(4):303-10.

Monosomy G: case report and review of the literature.

J Med Genet. 1971 Dec;8(4):496-500. doi: 10.1136/jmg.8.4.496.

Group G deletion syndromes.

J Med Genet. 1971 Sep;8(3):341-5. doi: 10.1136/jmg.8.3.341.

A child with a ring G chromosome (46,XX, Gr).

J Med Genet. 1971 Jun;8(2):231-4. doi: 10.1136/jmg.8.2.231.

A 45,XX,21--child: attempt at a cytological and clinical interpretation of the karyotype.

J Med Genet. 1972 Mar;9(1):110-5. doi: 10.1136/jmg.9.1.110.

Mental retardation, unusual facies, and abnormal nails associated with a group-G ring chromosome. A case report on two unrelated cases.

J Med Genet. 1971 Jun;8(2):195-201. doi: 10.1136/jmg.8.2.195.

[Ring G-chromosome. Report of two cases and review of literature].

Humangenetik. 1971;12(2):142-55. doi: 10.1007/BF00291470.

Karyotype 45,XX,-21/46,XX,21q-in an infant with symptoms of G-deletion syndrome I.

J Med Genet. 1974 Dec;11(4):389-93. doi: 10.1136/jmg.11.4.389.

A male infant with monosomy 21.

Humangenetik. 1975 Aug 29;29(1):1-7. doi: 10.1007/BF00273344.