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Results of search for 'au:"PFEIFFER, R A"', page 12 of 14
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Authors
Ammermann, M
BACHMANN, K D
Baisch, C
Ballhausen, W G
Beinder, E
Bier, L
Büchner, T
Diekmann, L
Henkel, K E
KOSENOW, W
Kessel, E
Lenz, W
Majewski, F
PFEIFFER, R A
Pfeiffer, R A
Rauch, A
Rott, H D
Stöss, H
Trautmann, U
Ulmer, R
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Topics
Abnormalities, Multiple
Adolescent
Adult
Child
Child, Preschool
Chromosome Aberrations
Chromosome Disorders
Female
Humans
Infant
Infant, Newborn
Intellectual Disability
Karyotyping
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Pedigree
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Trisomy
abnormalities
genetics
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Your search returned 274 results.
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221.
[Are monozygous twins and twin-specific abnormalities more prevalent following extracorporeal fertilization? A comment on studies of the Gynecologic Clinic of the Erlangen-Nürnberg University].
[electronic resource]
by
Pfeiffer, R A
Van Uem, J F
Siebzehnrübl, E
Wildt, L
Producer:
19891221
In:
Geburtshilfe und Frauenheilkunde
vol. 49
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222.
Mosaicism for an additional partial chromosome 8: 46,XX/47,XX+der(8)(p21 leads to qter).
[electronic resource]
by
Pfeiffer, R A
Kessel, E
Rathgen, E
Kulenkampff, M
Nehring, T
Producer:
19790324
In:
Human genetics
vol. 44
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223.
Human Y chromosomes with two fluorescing bands after staining with quinacrine derivates.
[electronic resource]
by
Kim, M A
Bier, L
Pawlowitzki, I H
Pfeiffer, R A
Producer:
19720106
In:
Humangenetik
vol. 13
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224.
Studies of malformation syndromes of man XXIV B: the Dubowitz syndrome. Further observations.
[electronic resource]
by
Opitz, J M
Pfeiffer, R A
Hermann, J P
Kushnick, T
Producer:
19740308
In:
Zeitschrift fur Kinderheilkunde
vol. 116
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225.
Familial reciprocal translocation t(17;19) (q11.2;q13.2) associated with neurofibromatosis type 1, including one patient with non-Hodgkin lymphoma and an additional t(14;20) in B lymphocytes.
[electronic resource]
by
Fahsold, R
Habash, T
Trautmann, U
Haustein, A
Pfeiffer, R A
Producer:
19950817
In:
Human genetics
vol. 96
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226.
[Coloboma and anal atresia: phenotype of a chromosome aberration?].
[electronic resource]
by
Pfeiffer, R A
Heimann, K
Heiming, E
Schlack, H
Maul, H
Producer:
19720501
In:
Klinische Monatsblatter fur Augenheilkunde
vol. 159
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227.
Multiple (up to seven) different accessory small marker chromosomes: prenatal diagnosis and follow-up.
[electronic resource]
by
Ulmer, R
Pfeiffer, R A
Wiest, E
Goelz, R
Trautmann, U
Producer:
19970918
In:
Annales de genetique
vol. 40
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228.
The Zimmermann-Laband syndrome.
[electronic resource]
by
Pfeiffer, R A
Seemanova, E
Süss, J
Müssig, D
Tietze, H U
Producer:
19920326
In:
Klinische Padiatrie
vol. 204
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229.
Identification of a de novo insertional mutation in P0 in a patient with a Déjérine-Sottas syndrome (DSS) phenotype.
[electronic resource]
by
Rautenstrauss, B
Nelis, E
Grehl, H
Pfeiffer, R A
Van Broeckhoven, C
Producer:
19950228
In:
Human molecular genetics
vol. 3
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230.
Robinow or "fetal face syndrome" in a male infant with ambiguous genitalia and androgen receptor deficiency.
[electronic resource]
by
Schönau, E
Pfeiffer, R A
Schweikert, H U
Böwing, B
Schott, G
Producer:
19900828
In:
European journal of pediatrics
vol. 149
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231.
[Connatal ptosis: a symptom of the syndrome of multiple pterygium and arthrogryposes].
[electronic resource]
by
Böckel, J
Grassl, F
Pfeiffer, R A
Ruprecht, K W
Heidbreder, E
Producer:
19841115
In:
Klinische Monatsblatter fur Augenheilkunde
vol. 185
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232.
Combination of silver and fluorescent staining for metaphase chromosomes.
[electronic resource]
by
Lau, Y F
Pfeiffer, R A
Arrighi, F E
Hsu, T C
Producer:
19780329
In:
American journal of human genetics
vol. 30
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233.
[Acrocephalopolysyndactyly (type II (McKusick) acrocephalosyndactyly or Carpenter's syndrome. Report on 4 cases and an observation of the syndrome of Marshall-Smith (author's transl)].
[electronic resource]
by
Pfeiffer, R A
Seemann, K B
Tünte, W
Gussone, J
Klemm, E
Producer:
19770622
In:
Klinische Padiatrie
vol. 189
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234.
[Hypothalamo-hypophyseal dwarfism with inner ear deafness in 2 sisters].
[electronic resource]
by
Winkelmann, W
Solbach, H G
Wiegelmann, W
Bethge, H
Pfeiffer, R A
Producer:
19720725
In:
Der Internist
vol. 13
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235.
Nosology of congenital non-progressive cerebellar ataxia. Report on six cases in three families.
[electronic resource]
by
Pfeiffer, R A
Palm, D
Jünemann, G
Mandl-Kramer, S
Heimann, E
Producer:
19740604
In:
Neuropadiatrie
vol. 5
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236.
[Familial cardiomyopathy with congenital webbed neck].
[electronic resource]
by
Diekmann, L
Pfeiffer, R A
Hilgenberg, F
Bender, F
Reploh, H D
Producer:
19681010
In:
Munchener medizinische Wochenschrift (1950)
vol. 109
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237.
Triploid embryo after in vitro fertilization.
[electronic resource]
by
Ulmer, R
Rehder, H
Trotnow, S
Kniewald, A
Kniewald, T
Pfeiffer, R A
Producer:
19860130
In:
Archives of gynecology
vol. 237
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238.
[Polysyndactyly, short limbs, and genital malformations--a new syndrome?].
[electronic resource]
by
Majewski, F
Pfeiffer, R A
Lenz, W
Müller, R
Feil, G
Seiler, R
Producer:
19720217
In:
Zeitschrift fur Kinderheilkunde
vol. 111
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239.
A novel 22q11.2 microdeletion in DiGeorge syndrome.
[electronic resource]
by
Rauch, A
Pfeiffer, R A
Leipold, G
Singer, H
Tigges, M
Hofbeck, M
Producer:
19990413
In:
American journal of human genetics
vol. 64
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240.
[Mongolism and leukemia. Clinical and cytogenetic findings in 4 mongoloid children with leukemia].
[electronic resource]
by
Hellriegel, K P
Pfeiffer, R A
Seiler, R
Schütz, C
Rickers, H J
Producer:
19691021
In:
Munchener medizinische Wochenschrift (1950)
vol. 111
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