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X
Tariverdian, Gholamali
36  Ergebnisse:
Personensuche X
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1

Trisomy 8q and partial trisomy 22 in a 43‐year‐old man with..:

Helbig, Ingo ; Wirtenberger, Michael ; Jauch, Anna...
American Journal of Medical Genetics Part A.  140A (2006)  15 - p. 1658-1662 , 2006
Link: https://doi.org/10.1002/..
 
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2

Multicolor chromosomal bar coding characterizes a de novo i..:

Schiffer, Christiane ; Popp, Susanne ; Moshir, Sharareh...
Clinical Dysmorphology.  12 (2003)  2 - p. 129-131 , 2003
Link: https://doi.org/10.1097/..
 
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3

Holoprosencephaly, bilateral cleft lip and palate and ectro..:

K??nig, Rainer ; Beeg, Thomas ; Tariverdian, Gholamali..
Clinical Dysmorphology.  12 (2003)  4 - p. 221-225 , 2003
Link: https://doi.org/10.1097/..
 
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4

The Novel Rho-GTPase Activating Gene MEGAP/srGAP3 Has a Put..:

Endris, Volker ; Wogatzky, Birgit ; Leimer, Uwe...
Proceedings of the National Academy of Sciences of the United States of America.  99 (2002)  18 - p. 11754-11759 , 2002
Link: https://www.jstor.org/st..
 
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5

Study of 30 patients with unexplained developmental delay a..:

Popp, Susanne ; Schulze, Birgit ; Granzow, Martin...
Human Genetics.  111 (2002)  1 - p. 31-39 , 2002
Link: https://doi.org/10.1007/..
 
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6

The novel Rho-GTPase activating geneMEGAP/srGAP3has a putat..:

Endris, Volker ; Wogatzky, Birgit ; Leimer, Uwe...
Proceedings of the National Academy of Sciences.  99 (2002)  18 - p. 11754-11759 , 2002
Link: https://doi.org/10.1073/..
 
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7

Agnathia‐otocephaly complex: Report of three cases with inv..:

Schiffer, Christiane ; Tariverdian, Gholamali ; Schiesser, Monika..
American Journal of Medical Genetics.  112 (2002)  2 - p. 203-208 , 2002
Link: https://doi.org/10.1002/..
 
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8

Misclassification risk of patients with bilateral cleft lip..:

Schulze, Birgit R. B. ; Tariverdian, Gholamali ; Komposch, Gerda.
American Journal of Medical Genetics.  99 (2001)  4 - p. 280-285 , 2001
Link: https://doi.org/10.1002/..
 
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9

Ellis-van Creveld syndrome: a generalized dysplasia of ench..:

Sergi, C. ; Voigtländer, Theda ; Zoubaa, Saida...
Pediatric Radiology.  31 (2001)  4 - p. 289-293 , 2001
Link: https://doi.org/10.1007/..
 
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10

Multiplex FISH telomere integrity assay identifies an unbal..:

Granzow, Martin ; Popp, Susanne ; Keller, Monika...
Human Genetics.  107 (2000)  1 - p. 51-57 , 2000
Link: https://doi.org/10.1007/..
 
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11

A case of Perlman syndrome: Fetal gigantism, renal dysplasi..:

Schilke, Kathrin ; Schaefer, Franz ; Waldherr, R�diger...
American Journal of Medical Genetics.  91 (2000)  1 - p. 29-33 , 2000
Link: https://doi.org/10.1002/..
 
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12

Rare dental abnormalities seen in oculo-facio-cardio-dental..:

Schulze, Birgit R.B. ; Horn, Denise ; Kobelt, Albrecht..
American Journal of Medical Genetics.  82 (1999)  5 - p. 429-435 , 1999
Link: https://doi.org/10.1002/..
 
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13

L�ri-Weill syndrome as part of a contiguous gene syndrome a..:

Spranger, Stephanie ; Schiller, Simone ; Jauch, Anna...
American Journal of Medical Genetics.  83 (1999)  5 - p. 367-371 , 1999
Link: https://doi.org/10.1002/..
 
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14

Short-rib-polydactyly syndrome type Verma-Naumoff-Le Marec ..:

Hentze, Sabine ; Sergi, Consolato ; Troeger, Jochen...
American Journal of Medical Genetics.  80 (1998)  3 - p. 281-285 , 1998
Link: https://doi.org/10.1002/..
 
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15

Monoallelic Expression of HumanPEG1/MESTIs Paralleled by Pa..:

Riesewijk, Anne M. ; Hu, Landian ; Schulz, Ute...
Genomics.  42 (1997)  2 - p. 236-244 , 1997
Link: https://doi.org/10.1006/..
 
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