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Items: 14

3.

Chromosomal aberrations in couples undergoing intracytoplasmic sperm injection: influence on implantation and ongoing pregnancy rates.

Scholtes MC, Behrend C, Dietzel-Dahmen J, van Hoogstraten DG, Marx K, Wohlers S, Verhoeven H, Zeilmaker GH.

Fertil Steril. 1998 Nov;70(5):933-7.

PMID:
9806579
4.

Clarification of subtle reciprocal rearrangements using fluorescence in situ hybridization.

Sullivan BA, Leana-Cox J, Schwartz S.

Am J Med Genet. 1993 Aug 15;47(2):223-30.

PMID:
8213910
5.

Meiotic segregation in familial reciprocal translocation t(8q;22q).

Gödde-Salz E, Oesinghaus S, Grote W.

Am J Med Genet. 1982 Feb;11(2):241-7.

PMID:
7065009
7.

Partial trisomy 8 (8q24) and the trisomy-8 syndrome.

Sánchez O, Yunis JJ.

Humangenetik. 1974;23(4):297-303. No abstract available.

PMID:
4420964
8.

Cloning defined regions of the human genome by microdissection of banded chromosomes and enzymatic amplification.

Lüdecke HJ, Senger G, Claussen U, Horsthemke B.

Nature. 1989 Mar 23;338(6213):348-50.

PMID:
2784197
10.

Partial deletion 8q without Langer-Giedion syndrome: a recognisable syndrome.

Fennell SJ, Benson JW, Kindley AD, Schwarz MJ, Czepulkowski B.

J Med Genet. 1989 Mar;26(3):167-71. Review.

11.

The importance of further cytogenetic and molecular investigation of acrocentric variants: justification by presentation of a case [t(8;14)(q24;p11)].

Hills L, Earle E, Wilson M, Petrovic V, Voullaire LE, Leversha M, Danks DM, Choo KH.

Hum Genet. 1991 Jun;87(2):173-6.

PMID:
2066104
12.

Molecular analysis of overlapping chromosomal deletions in patients with Langer-Giedion syndrome.

Parrish JE, Wagner MJ, Hecht JT, Scott CI Jr, Wells DE.

Genomics. 1991 Sep;11(1):54-61.

PMID:
1684953
13.

Chromosome abnormalities and rare fragile sites detected in azoospermia patients.

Seki N, Sumiya H, Shimazaki J, Toyama Y, Takahashi E, Murata M, Hori T.

Jpn J Hum Genet. 1992 Sep;37(3):215-22.

PMID:
1472703
14.

[Chromosome 8 : complete trisomy and segmental trisomies].

Rethoré MO, Aurias A, Couturier J, Dutrillaux B, Prieur M, Lejeune J.

Ann Genet. 1977 Mar;20(1):5-11. French.

PMID:
302674

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