Schwanitz G - Search Results

1

Prenatal diagnosis and management in fetuses with cystic hygromata colli.

Gembruch U, Hansmann M, Bald R, Zerres K, Schwanitz G, Födisch HJ. Gembruch U, et al. Among authors: schwanitz g. Eur J Obstet Gynecol Reprod Biol. 1988 Dec;29(4):241-55. doi: 10.1016/0028-2243(88)90064-0. Eur J Obstet Gynecol Reprod Biol. 1988. PMID: 3068081

2

Chromosomal findings in fetuses with prenatally diagnosed cysts of the choroid plexus.

Zerres K, Schüler H, Gembruch U, Bald R, Hansmann M, Schwanitz G. Zerres K, et al. Among authors: schwanitz g. Hum Genet. 1992 May;89(3):301-4. doi: 10.1007/BF00220545. Hum Genet. 1992. PMID: 1601421 Review.

3

Prenatal detection of heart defects as an indication for chromosome analysis.

Schwanitz G, Zerres K, Gembruch U, Bald R, Gamerdinger F, Hansmann M. Schwanitz G, et al. Ann Genet. 1990;33(2):79-83. Ann Genet. 1990. PMID: 2146918

4

Rate of chromosomal aberrations in prenatally detected hydrops fetalis and hygroma colli.

Schwanitz G, Zerres K, Gembruch U, Bald R, Hansmann M. Schwanitz G, et al. Hum Genet. 1989 Dec;84(1):81-2. doi: 10.1007/BF00210678. Hum Genet. 1989. PMID: 2606481

5

[Trisomy 22--prenatal findings in various developmental stages].

Zerres K, Niesen M, Schwanitz G, Hansmann M. Zerres K, et al. Among authors: schwanitz g. Geburtshilfe Frauenheilkd. 1988 Oct;48(10):720-3. doi: 10.1055/s-2008-1026616. Geburtshilfe Frauenheilkd. 1988. PMID: 3234704 German.

6

Chromosomal findings in fetuses with ultrasonographically diagnosed ventriculomegaly.

Schwanitz G, Schüler H, Gembruch U, Zerres K. Schwanitz G, et al. Ann Genet. 1993;36(3):150-3. Ann Genet. 1993. PMID: 8117059 Review.

7

[Fetal echocardiography and clinical genetics--a close correlation].

Zerres K, Gembruch U, Schwanitz G, Redel DA, Bald R, Gottschlich A, Hansmann M. Zerres K, et al. Among authors: schwanitz g. Z Kardiol. 1990 Feb;79(2):96-106. Z Kardiol. 1990. PMID: 2321416 German.

8

Hydrops fetalis as an indication for prenatal chromosome analysis with the example of the diagnosis of a duplication 15q11 and 17q25 due to a familial translocation 15/17.

Schwanitz G, Zerres K, Niesen M, Haverkamp F, Schmid G. Schwanitz G, et al. Ann Genet. 1988;31(3):186-9. Ann Genet. 1988. PMID: 3066282

9

Partial monosomy 22 as result of an X/22 translocation in a newborn with DiGeorge syndrome.

Schwanitz G, Zerres K. Schwanitz G, et al. Ann Genet. 1987;30(2):80-4. Ann Genet. 1987. PMID: 3314667 Review.

10

[Non-immunologic hydrops fetalis (NIHF)--case report of double partial trisomy 15q and 17q resulting from familial translocation 15/17 and cytogenetic findings in 50 cases with hydrops fetalis].

Schmid G, Haverkamp F, Rechmann J, Schwanitz G, Zerres K, Hansmann M, Kowalewski S. Schmid G, et al. Among authors: schwanitz g. Klin Padiatr. 1987 Jul-Aug;199(4):309-14. doi: 10.1055/s-2008-1026810. Klin Padiatr. 1987. PMID: 3657040 German.

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